{ "count" : 6257, "data" : [ { "id" : "6a30706df292fd229cff4aa0", "title" : "Chemical Operator", "company" : "Standard Nuclear, Inc.", "salary" : { "min" : 65000.0, "max" : 95000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for a Chemical Operator in Idaho Falls, USA, with adjustments for mid-seniority and the manufacturing industry." }, "location" : "Scoville, Idaho, United States", "locations" : [ "Scoville", "Idaho", "United States" ], "timestamp" : "2026-06-16T12:06:51.372", "fingerprint" : "9cd8c8ab76ee3834ad99c198a0e3c7e6b7ed5d6a73979a5e90dd576406765e81", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/standardnuclearinc/jobs/5263527008", "externalId" : "5263527008", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Idaho Falls", "state" : "Idaho", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.4887907,-112.0362800" } ], "locationText" : "Idaho Falls, Idaho, United States", "employmentType" : "FULL_TIME", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Location: Idaho Falls, ID Schedule: Full-Time FUNCTION The Chemical Operator will support Standard Nuclear’s chemical processing and materials production operations by operating, monitoring, and maintaining equipment used in sol-gel processing and chemical dissolution systems. This is a hands-on role involving solution mixing, reactor operation, particulate washing and drying, filtration, liquid waste handling, and general materials processing. Operators will be cross-trained across multiple systems and will support operations in Standard Nuclear’s Idaho Facility to ensure consistent production output. This position requires mechanical aptitude, attention to detail, and the ability to follow procedures closely. Prior experience with the specific equipment or processes is not required — strong operators from chemical, industrial, or manufacturing environments are encouraged to apply. RESPONSIBILITIES Sol-Gel & Dissolution Operations Operate equipment used in sol-gel processing, including mixers, vibratory pumps, wash systems, heating/drying units, and filtration systems. Prepare chemical solutions by measuring, mixing, and adjusting feed components according to established procedures. Support dissolution processes involving powders, aqueous solutions, and controlled chemical reactions. Perform washing steps using oxide solutions and rinsing equipment to clean or condition material batches. Chemical Handling & Process Execution Handle chemical powders, solutions, and liquid waste streams following approved safety practices. Monitor process parameters, system pressures, solution levels, temperatures, and flow rates. Document batch data, equipment readings, and process deviations accurately. Conduct routine cleaning, equipment resets, and system preparation between production runs. Equipment Operation & Troubleshooting Operate pumps, valves, pneumatic systems, heaters, furnaces, filtration modules, and separation equipment. Perform basic troubleshooting on mechanical and chemical processing systems. Assist maintenance or engineering staff with system adjustments, repairs, or calibration activities. Safety, Quality & Compliance Follow all Standard Nuclear environmental, health, and safety (EH&S) requirements, including hazardous material handling and PPE protocols. Maintain accurate records in accordance with quality assurance procedures. Support internal audits, inspections, and readiness reviews. Adhere strictly to written procedures and report any deviations or safety concerns immediately. Cross-Training & Production Support Train across multiple chemical processing areas to provide operational flexibility. Support production operations across Standard Nuclear’s Idaho facility as needed. Collaborate with engineering, quality, and operations teams to improve process consistency and efficiency. PREFERED QUALIFICATIONS (No degree required — candidates from manufacturing, chemical processing, or industrial operations are encouraged to apply.) Minimum Requirements 3+ years of experience in chemical processing, industrial manufacturing, or mechanical/process operations. Ability to safely handle powders, solutions, pumps, mixers, and industrial processing equipment. Familiarity with basic chemical handling and general industrial safety practices. Comfortable working with wash solutions, liquid waste systems, and cleaning processes. Ability to follow detailed procedures and record accurate operational data. Ability to lift 50 lbs., work at heights, and work in environments involving heat, noise, or odors. Ability to work in controlled or restricted areas with required PPE. Preferred Experience (Not Required) Experience in sol-gel processing, wet chemistry, or materials processing. Prior work with reactors, mixing systems, dry/wet separation equipment, or filtration modules. Experience in plant start-up, new equipment commissioning, or scale-up environments. Exposure to regulated operations (NQA-1, ISO, cGMP, etc.). Lean/Six Sigma or continuous improvement familiarity. BENEFITS Health, Dental & Vision Insurance Health Savings Account Disability and Life Insurance 401K Plan Paid Time Off, Holidays WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Work is performed in chemical processing and industrial manufacturing areas. PPE such as gloves, safety glasses, and respirators may be required. Some work occurs in controlled or restricted-access environments involving powders and chemical solutions. Standard Nuclear embraces equal opportunity and is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability, or any other legally protected status. To conform to U. S. Government export regulations, applicant must be a U. S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S. C. 1324b(a)(3), or eligible to obtain the required authorizations from the U. S. Department of State.", "summaryDescription" : "Chemical Operator at Standard Nuclear, Inc.", "postedDate" : "2026-06-16T01:18:13.012", "createdAt" : "2026-06-16T01:18:13.012", "lastUpdated" : "2026-06-16T12:06:51.372", "ingestTimestamp" : "2026-06-16T01:18:13.012", "mongoId" : "6a30706df292fd229cff4aa0", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 65000, "salaryAnnualMax" : 95000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Manufacturing", "llmIndustryConfidence" : 0.95 }, { "id" : "6a305611f292fd229cf2497e", "title" : "Clinical Assay Performance Fellow", "company" : "Moderna", "industry" : "Biotech", "salary" : { "min" : 30000.0, "max" : 45000.0, "currency" : "GBP", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimation is based on the UK market baseline for an entry-level Clinical Assay Performance Fellow in the Biotech industry, adjusted for company size and internship employment type." }, "location" : "United Kingdom", "locations" : [ "United Kingdom" ], "timestamp" : "2026-06-16T13:53:46.192", "fingerprint" : "00e70227ab5620d7328392c8ce07f08dbf4f542f7af2c7751ed0f2ffdf402493", "source" : "workday", "language" : "en", "applyUrl" : "https://modernatx.wd1.myworkdayjobs.com/M_tx/job/Oxford---England/Clinical-Assay-Performance-Fellow_R19323-1", "externalId" : "R19323", "industryFunction" : { }, "locationPoint" : "55.3781,-3.436", "structuredLocations" : [ { "country" : "United Kingdom", "continent" : "eu", "workMode" : "onsite" } ], "locationText" : "United Kingdom", "employmentType" : "FULL_TIME", "remoteFriendly" : false, "rawDescription" : "**The Role** This short-term internship will support a focused project on assay performance monitoring and digital enablement across the Clinical Biomarker Laboratories (CBL). You will evaluate current approaches to assay performance tracking (e.g. trending, control data, variability) and develop a simple, scalable digital solution to improve visibility, standardisation, and transferability across functional assay teams. The work will be grounded in real datasets and laboratory workflows, with a focus on practical implementation and exploration of AI-driven approaches where appropriate. **What You’ll Gain** * Exposure to a regulated clinical testing environment (GxP) * Understanding of assay performance and lifecycle monitoring across multiple platforms * Experience working at the interface of science, data, and digital/AI solutions * Visibility and interaction with cross-functional stakeholders involved in clinical testing * Opportunity to deliver a tangible output with potential application across CBL teams **Here’s What You’ll Do** Working with scientists and cross-functional stakeholders, you will: * Review current assay performance monitoring and data trending approaches. * Engage with Flow Cytometry, Immunoassay teams to understand workflows and data structures. * Identify gaps in standardisation, data access, and cross-team usability. * Design and prototype a digital solution (e.g. dashboard, automated trending, AI-supported insights) * Explore AI/data-driven approaches to detect drift, variability, or performance issues * Support laboratory-based activities under supervision to understand assay execution and data generation. * Present a final recommendation and/or working prototype. You will interact with stakeholders across Moderna’s clinical testing functions (Assay Leads, Study Leads, Operations, Automation, Compliance) to ensure solutions are aligned to practical use. **Here’s What You’ll Need (Minimum Qualifications)** * Background in science, engineering, or data science (e.g. biology, physics) * Interest in data, digital tools, or AI * Strong analytical and problem-solving skills * Able to work independently and synthesise input from multiple stakeholders **Pay & Benefits** **At Moderna, we believe that when you feel your best, you can do your best work. That’s why our global benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.** * Best-in-class healthcare, plus voluntary benefit programs to support your unique needs * A holistic approach to well-being with access to fitness, mindfulness, and mental health support * Family building benefits, including fertility, adoption, and surrogacy support * Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown * Savings and investments to help you plan for the future * Location-specific perks and extras The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work. **About Moderna** Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities. We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit [modernatx.com/careers](https://www.modernatx.com/en-US/careers/life-at-moderna) to learn more about our current opportunities. Moderna is a smoke-free, alcohol-free, and drug-free work environment. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply! Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best. Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at [leavesandaccommodations@modernatx.com](mailto:leavesandaccommodations@modernatx.com%22%20\\\\o%20%22mailto:leavesandaccommodations@modernatx.com%22%20\\\\t%20%22_blank). -", "summaryDescription" : "Clinical Assay Performance Fellow at Moderna", "postedDate" : "2026-06-13T03:47:09.529", "createdAt" : "2026-06-16T03:47:09.523", "lastUpdated" : "2026-06-16T13:53:46.192", "ingestTimestamp" : "2026-06-16T03:47:09.523", "mongoId" : "6a305611f292fd229cf2497e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://modernatx.wd1.myworkdayjobs.com/M_tx/job/Oxford---England/Clinical-Assay-Performance-Fellow_R19323-1", "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "mid", "dataQualityScore" : 0.7777778, "daysOld" : 3, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2eb38e74d8ee00a0e7ea6d", "title" : "Assembler II (Non-Routine)", "company" : "A-dec", "salary" : { "min" : 45000.0, "max" : 60000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Assembler II in the United States, adjusted for junior seniority and the healthcare industry." }, "location" : "United States of America", "locations" : [ "United States of America" ], "timestamp" : "2026-06-16T00:43:58.049", "fingerprint" : "e6d6a7082ad0465f0b66901520ddc59745e637754c054930cfbbe0f6c7df4abd", "source" : "workday", "language" : "en", "applyUrl" : "https://adec.wd5.myworkdayjobs.com/A-dec/job/Oregon---Newberg-Campus/Assembler-II--Non-Routine-_JR102346-1", "externalId" : "JR102346", "industryFunction" : { }, "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "onsite" } ], "locationText" : "United States", "employmentType" : "FULL_TIME", "remoteFriendly" : false, "rawDescription" : "At A-dec, we do more than create the highest quality products and services for the dental industry; we strive to deliver a superior employment experience for each of our team members. With an environment that encourages and assists each person in developing to their highest potential, a career at A-dec is incredibly rewarding. ## Overview The Assembler II performs both routine and semi-routine assembly tasks which include sub-assemblies, assembling some final products, packaging, water spider, and checks parts for quality and function. **JOB DUTIES AND RESPONSIBILITIES:** * Performs routine assembly tasks, working independently with the aid of standard work assembly drawings (SWADs), such as: * Assembles electrical and mechanical components and any additional routine sub-assemblies. * Packages products while maintaining quality and productivity standards. * Water Spider (inventory movement support): facilitates workflow, including stocking bins, pallets, cardboard, and general material handling. * Builds final product. Works with area manufacturing engineers (ME’s) * Frequently operates tools/equipment such as hand tools, pneumatics tools, testing equipment, fixtures, and high voltage dielectric testing while using required personal protective equipment (PPE) and following safety guidelines. * Routinely follows work and test instructions to perform tasks. May be required to interpret the results of certain tests and at times may troubleshoot and repair assemblies as necessary. * Achieves and maintains established safety, quality, and productivity standards. Must not pose a risk to self or others. * Assembler II is in the process of learning to build an entire product or line and may train less experienced Assemblers. **QUALIFICATIONS:** **Knowledge, Skills, and Abilities** * Must be able to read, write, and communicate in English with a demonstrated ability to follow written and oral instructions. * Must possess basic computer skills. * Able to perform basic math calculations. * Must be able to troubleshoot problems when necessary. * Must be able to operate the required hand tools and fixtures. * Able to interpret standard work assembly drawings (SWAD), production order paperwork, test instructions, and quality checklists. **Education and Experience** * Typically requires 1-2 years of manufacturing experience. **Physical Requirements:** Ability to lift, carry, push, pull or otherwise maneuver up to 35 pounds with or without assistance on a routine basis. Must have manual hand dexterity to grasp, operate tools and equipment repetitively. Able to walk, stand, sit, bend, reach, and occasionally kneel, climb steps, and twist throughout an entire shift. Some areas may be exposed to chemicals, noise, vibration and /or dust, and require the use of appropriate Personal Protective Equipment (PPE); such as, but not limited to safety glasses, hearing protection, foot protection, etc. **Disclaimer** This job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not to be construed as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to this job. A-dec reserves the right to assign job duties and days and hours of work based on factors such as workload requirements, staffing levels, and customer demands. At A-dec, we value our people and show it by prioritizing an inclusive culture, total well-being, and opportunities for learning and career advancement. **A background check and screen for the illegal use of drugs is required.** _A-dec is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. In addition, A-dec will not discriminate against applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another. *VEVRAA Federal Contractor”_ _A-dec is interested in qualified candidates authorized to work in the United States for US-based positions. We are unable to sponsor or take over sponsorship of employment visas._", "summaryDescription" : "Assembler II (Non-Routine) at A-dec", "postedDate" : "2026-06-12T22:08:37.838", "createdAt" : "2026-06-14T22:08:37.806", "lastUpdated" : "2026-06-16T00:43:58.049", "ingestTimestamp" : "2026-06-14T22:08:37.806", "mongoId" : "6a2eb38e74d8ee00a0e7ea6d", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://adec.wd5.myworkdayjobs.com/A-dec/job/Oregon---Newberg-Campus/Assembler-II--Non-Routine-_JR102346-1", "salaryAnnualMin" : 45000, "salaryAnnualMax" : 60000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "mid", "dataQualityScore" : 0.7777778, "daysOld" : 3, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c6c3b74d8ee00a09179ba", "title" : "Chemical Technician", "company" : "Triumvirate Environmental", "salary" : { "min" : 28.0, "max" : 28.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Niagara Falls, Ontario, Canada", "locations" : [ "Niagara Falls", "Ontario", "Canada" ], "timestamp" : "2026-06-16T00:49:18.680", "fingerprint" : "64da15e8546025077199fc928cd5ec01b681caf5a4e50ff97bbf5246e657be36", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/triumvirateenvironmental/jobs/4684623006", "externalId" : "4684623006", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Niagara Falls", "state" : "Ontario", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.1065603,-79.0639039" } ], "locationText" : "Niagara Falls, Ontario, Canada", "remoteFriendly" : false, "rawDescription" : "Chemical Technician Photech Environmental Services Inc, a wholly owned subsidiary of Triumvirate Environmental, one of the largest environmental services firms in North America, is seeking a Chemical Technician to join our team at our Niagara Falls, ON location. Photech Environmental Solutions provides hazardous waste disposal services to industrial, research and institutional facilities across Ontario, where chemical wastes are sorted, packaged and removed from generator facilities and shipped to our hazardous waste transfer and processing facility in Niagara Falls, ON. Photech employs highly skilled chemical technicians who work within our Lab Pack processing operations, where a Lab Pack is then manually deconstructed for bulk consolidation within our Lab Pack production space. The chemical technician is responsible for oversight and delivery of the entire process. The deconstruction and consolidation process requires experienced Chemical Technicians to sort through bins containing bottles of chemical wastes, separating for bulking chemical compatibility and disposal/recycling treatment technology. Chemicals are re-sorted into similar bins and labelled for the appropriate bulking station. Full bins are pushed further ahead on the manual roller conveyor to the end, where bins await labpack labourers who are tasked with the opening and bulking of segregated chemical wastes at designated bulking stations Responsibilities: Work as part of a team in a chemical waste consolidation/processing area. Work under difficult seasonal environment conditions (hot/cold) The donning and use of task specific PPE, including but not limited to: Full face respiratory protection, Poly Coated Tyvek PPE, Hard Hat, CSA approved Safety Boots. Conduct onsite evaluations to assess, categorize and segregate hazardous waste materials by chemical compatibility and disposition streaming. Safely consolidate processable segregated waste for disposition. Safely repack highly hazardous wastes for disposition. Prepare and label bulk waste containers according to regulatory requirements and company policies. Document and maintain accurate records of waste processing activities. Respond promptly and effectively to emergency situations involving hazardous materials. Safe operation of lift trucks. Occasional weekend work at company hosted household hazardous waste events across Ontario, providing technical chemical ID, segregation and packing services. Basic Requirements: Completion of a two- or three-year college program in chemical, biochemical or chemical engineering technology or a closely related discipline Experience with Ontario Regulation 347 of the Environmental Protection Act. Minimum 3 years experience in hazardous waste processing and material handling. Must demonstrate strong verbal and written communication abilities to effectively interact with colleagues, and stakeholders, ensuring clear and professional exchanges of information Demonstrated ability to analyze complex issues, develop solutions, and implement strategies to achieve positive outcomes Valid provincial driver’s license Must be willing to consent to a criminal background check. Ability to lift 50 pounds on a regular basis Ability to work overtime on a regular basis Must be clean-shaven and able to wear all required safety equipment in both hot and cold temperatures during regular working conditions. The Lab Pack Specialist frequently handles hazardous chemicals and is responsible for donning and doffing personal protective equipment in both hot and cold work environments. This role is considered safety-sensitive Preferred Requirements: Besides Health, Dental and Vision benefits, TONS of safety training for some positions with opportunities for external trainings and certifications, Mentorship & Career Succession Planning. To learn more about our business, culture, and the exciting work that we are doing in the industry, find us on LinkedIn, Instagram (@triumvirateenvironmental), or our website! Triumvirate Environmental is an equal opportunity employer. We are committed to fostering a diverse and inclusive workplace and encourage applications from individuals of all backgrounds, including women, racialized persons, Indigenous peoples, persons with disabilities, and members of the LGBTQ2S+ community. In accordance with the Accessibility for Ontarians with Disabilities Act (AODA), accommodation will be provided at any stage of the hiring process upon request. If you have a disability and need accommodation during the application and hiring process, please contact us at https://www.triumvirate.com/contact or call us at 888-834-9697. The requirements listed above are representative of the knowledge, skill, and/or ability required. Actual starting base pay may vary based on factors such as education, experience, skills, location and budget. 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We publish the largest number of journals and books and are pioneers in open research. Through our leading brands, trusted for more than 180 years, we provide technology-enabled products, platforms, and services that help researchers uncover new ideas and share their discoveries, advance science, and support education and healthcare globally. For more information, please visit about.springernature.com and follow @SpringerNature. **About the Brand** Nature Portfolio publishes high-quality, impactful research across the life, physical, chemical, and applied sciences. Its portfolio includes Nature, the Nature Research journals, Nature Reviews journals, Nature Communications, and Scientific Reports. Together, these journals publish some of the world’s most significant scientific discoveries. Online, nature.com provides millions of readers monthly with research content, news, commentary, and career opportunities via Nature Careers. For more information, please visit nature.com and follow @NaturePortfolio. **About the Role** Nature Communications is the leading multidisciplinary Open Access journal, publishing high-quality scientific research. To help build on the success of the journal, we are seeking a scientist with a background in biocatalysis, enzyme engineering, chemoenzymatic synthesis, computational chemistry applied to biological systems, or related areas at the chemistry-biology interface. The successful candidate will have a critical eye, a deep understanding of their subject area, broad scientific interests, and the ability to think on their feet. The Interim Associate or Senior Editor role at Nature Communications is ideal for researchers who love science but feel that a career at the bench is not enough to satisfy their desire to learn more about the natural world, and for those who enjoy reading papers outside their chosen area of research. **Role Responsibilities:** • Handle original research papers and oversee peer review • Work closely with other editors on all aspects of the editorial process, including manuscript selection • Make well-reasoned editorial decisions based on expert advice • Determine subject representation within the journal • Liaise extensively with editors across Nature Portfolio and the wider scientific community • Attend conferences and visit research institutions **Experience, Skills & Qualifications** **Essential:** • PhD (or equivalent) in biocatalysis, enzyme engineering, chemoenzymatic synthesis, computational chemistry applied to biological systems, or a related discipline at the chemistry-biology interface • Strong understanding of chemical biology and related research areas • Ability to critically assess the novelty, context, and impact of research • Excellent communication skills in written and spoken English • Strong interest in scientific research beyond a primary area of expertise • Ability to quickly engage with new research areas • Excellent interpersonal and collaboration skills • Willingness to travel and engage with researchers internationally **Desirable:** • Postdoctoral or equivalent research experience • Editorial experience (not required; full training will be provided) • Significant editorial experience may be considered for appointment at Senior Editor level To Apply, Please Submit: • CV • Cover letter explaining your motivation, preferred office location, salary expectations, and earliest start date At Springer Nature, we value diversity and inclusion and are committed to building an environment where everyone can thrive. We empower colleagues and value diverse perspectives as we strive to attract, nurture, and develop the very best talent. Springer Nature was awarded Diversity Team of the Year at the 2022 British Diversity Awards. More information: [https://group.springernature.com/gp/group/taking-responsibility/diversity-equity-inclusion](https://group.springernature.com/gp/group/taking-responsibility/diversity-equity-inclusion) If you have any access needs related to disability, neurodivergence, or a chronic condition, please contact us so we can make all necessary accommodations. For more information about career opportunities at Springer Nature, please visit: [https://careers.springernature.com/](https://careers.springernature.com/) #LI-MM1 Job Posting End Date: 30-06-2026", "summaryDescription" : "Interim Associate or Senior Editor, Nature Communications, Chemical Biology at Springer Nature. Skills: Chemical biology, Biocatalysis, Enzyme engineering. Handle original research papers. 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Self-perform teams; GC operations; Project stakeholders", "projectManagementSkills" : [ "Planning", "Scheduling", "Change management", "Closeout" ], "domainKnowledge" : "Commercial construction; Self-perform operations", "domainList" : [ "commercial-construction", "self-perform-operations" ], "domainSpecificKnowledge" : [ "Commercial construction", "Self-perform operations" ], "problemSolvingSkills" : "Risk planning; Resolve field issues", "specialRequirements" : "Background check, Drug screen", "outcomesObjectives" : "Successful delivery; Safety performance; Quality performance; Financial performance; Protect schedule; Protect margin", "qualificationsBasic" : "Bachelor's degree in Construction Management, Engineering, or related field, 10+ years of experience in commercial construction, Proven ability to manage complex scopes, Proven ability to manage labor productivity, Proven ability to manage cost performance, Relationship-building skills with owners, Relationship-building skills with architects, Relationship-building skills with field teams, Relationship-building skills with trade partners, Commitment to a safety-first culture, Disciplined execution in the field", "qualificationsPreferred" : "Proficiency in construction software, Experience with scheduling tools", "workSiteFlexibility" : "Onsite", "rawDescription" : "Celebrating 85 Years of Building With Purpose At Absher Construction, we’re proud to celebrate over 85 years as one of the Pacific Northwest’s most respected general contractors. As a 100% employee-owned company, we believe our people are our greatest asset and we invest in them like it! From fully paid medical premiums for employees, to a generous PTO policy, 401(k) and ESOP retirement benefits, we offer a total rewards package that reflects the pride and ownership we bring to every project. As a Self-Perform Project Manager, you own the outcome. You’ll lead Absher’s self-perform operations on multiple scopes, managing planning, performance, and profitability. This role is deeply rooted in the field where you’ll be walking jobs, pressure-testing plans, mentoring teams, and driving execution where it matters most. This is a builder’s role for someone who thrives on accountability, sees complexity as a challenge worth solving, and understands that high-performing teams are built through discipline, clarity, and collaboration. What You’ll Do Lead project execution to ensure successful delivery, safety, quality, and financial performance of self-perform scopes Oversee planning, scheduling, change management, safety integration, quality control, and closeout Develop and communicate execution strategies with field leaders to ensure clarity on scope, productivity goals, sequencing, and constraints Drive risk planning, identify high-risk activities early, and embed safety into crew planning and daily readiness Monitor and resolve field issues proactively, maintaining alignment between estimate, plan, and execution Track labor productivity and costs, identify variances, and implement corrective actions to protect schedule and margin Supervise, mentor, and develop team members to build the next generation of self-perform leaders Serve as the key interface between self-perform teams, GC operations, and project stakeholders, ensuring alignment and scope clarity Why You’ll Be Successful You’re not a spectator, you’re an operator. You lead with influence more than authority, thrive on solving complex challenges, and believe in building high-performing teams that win together. What You Bring: Bachelor’s degree in Construction Management, Engineering, or related field (or equivalent field experience) 10+ years of experience in commercial construction, preferably with self-perform operations Proven ability to manage complex scopes, labor productivity, and cost performance Strong relationship-building skills with owners, architects, field teams, and trade partners Commitment to a safety-first culture and disciplined execution in the field Proficiency in construction software (e.g., Procore, scheduling tools) a plus Safety certifications (OSHA 30, First Aid/CPR) preferred Note: Absher is a Federal Contractor. All job offers are contingent upon successful completion of a background check and drug screen. Salary offers are typically made between the entry and midpoint of the range and are based on factors such as experience, education, and internal equity. Pay Transparency $120,000—$150,000 USD Background Check & Pre-Employment Screening All offers of employment are contingent upon successful completion of a pre-employment background check and drug screening. Background checks may include verification of employment history, education, criminal records, and references. For positions with access to company financial accounts or credit card programs, a credit history check may also be conducted. All screening is conducted in compliance with the Fair Credit Reporting Act (FCRA) and applicable state and local laws. Candidates will be asked to provide written consent prior to any screening. If results include information that may affect a hiring decision, candidates will have the opportunity to review and respond to the findings before a final decision is made. Absher Construction is an equal opportunity employer. Background check results are evaluated in context and do not automatically disqualify applicants. Absher’s Commitment: Our Pledge to EEOC At Absher, we are committed to building a culture where everyone can thrive. We welcome diverse voices, perspectives, and experiences and we believe our work is stronger because of them. No employee or applicant will face discrimination based on race, color, national origin, religion, age, gender identity, sexual orientation, disability, veteran status, or any other protected class. Notice to Staffing Agencies Please note: We are not accepting unsolicited resumes or inquiries from staffing agencies at this time. Absher employees are not authorized to bind the company to any third-party recruitment agreements.", "summaryDescription" : "Concrete Project Manager - Self Perform Team at Absher Construction. Skills: Self-perform operations, Project execution, Field leadership. Lead project execution. 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Form Energy is an American manufacturing and energy technology company. We’re revolutionizing energy storage with cost-effective, multi-day technology designed to keep the electric grid secure and reliable, even during extended periods of stress. By strengthening the electric system and reimagining what’s possible, we’re giving clean energy a whole new form! In recent years, Form Energy has earned a number of accolades, including being named by TIME as a “Best Invention”, MIT Technology Review as a “Top Climate Tech Company To Watch”, and Fast Company as “One of the Next Big Things In Tech”. We are making rapid progress on our mission of delivering energy storage for a better world, and our team is growing just as rapidly to meet demand. We have signed contracts with leading electric utilities across the United States and production of our iron-air batteries is underway at our first high-volume manufacturing facility in West Virginia. Working for Form Energy is more than just a job, it’s a chance to be part of something extraordinary. And now - right as we significantly scale up battery manufacturing - might be the most exciting moment in the company’s history to join. We are assembling a team of highly talented and driven individuals across the country. Driven by our core values of humanity, excellence, and creativity, our team is determined to deliver on our mission and transform the energy landscape for the better. Feeling energized to make a meaningful impact on the world? Then keep reading - you’ve come to the right place. ROLE DESCRIPTION Form Energy is hiring a Senior Chemical Engineer to join the Product Echem Performance team. In this role, you will build on existing results to improve our electrolyte product integration process and help optimize the electrolyte workflow for Form Energy's long-duration energy storage system. As a Senior Chemical Engineer specializing in fluid mechanics, handling systems, and mathematical modeling, you will play a key role in developing and owning predictive models for our iron-air battery — including a shunt current model and an electrolyte level model — as well as designing and developing test vehicle components. Your responsibilities will also include leading the analysis and definition of requirements for fluid and material management, with modeling as a core tool for driving design decisions. This role is crucial in conducting hands-on verification testing to ensure that our fluid handling systems meet all requirements, and in closing gaps between model predictions and real-world test data. This role offers the chance to also work closely with chemical, materials, and mechanical engineers on the technology development team in the lab and to analyze their data. This is an exciting opportunity to help shape and be part of the growth of a fast-moving company with breakthrough technology and an incredible mission! Relocation assistance is available. WHAT YOU'LL DO: - Develop, own, and iterate on mathematical models to predict and analyze the behavior of fluid systems under different conditions, including a shunt current model and an dynamic fluid level model - Validate models against experimental data, perform root cause analysis when gaps arise, and drive model improvements - Establish processes and define system requirements to maintain chemical specifications throughout the battery's service lifetime - Execute chemistry and mechanical design trades, leveraging modeling to optimize the design of fluid handling components and interfaces between cells and systems - Provide high-quality data analysis and design trades WHAT YOU'LL BRING: - PhD or MS with 3+ years of professional experience in Chemistry, Chemical Engineering, Material Science or a related field is required - Expert in fluid mechanics, fluid handling and sensor selection - Experience in leading engineering verification tests, RCA and addressing model to data gap - Demonstrated experience with defining engineering requirements - Excellent problem solving and communication skills, and the ability to work both independently and collaboratively as part of a team #LI-Onsite Humanity is a cornerstone of Form Energy’s culture, and we make sure our compensation and benefits reflect that. Form Energy offers competitive salaries, stock options, and a holistic benefits package to ensure all employees have what they need to thrive while working here. When it comes to you and your family’s health, we cover 100% of medical, dental, and vision premiums for full-time employees - and 80% of healthcare premiums for dependents. This starts from day one. We also offer at least 12 weeks of paid leave for new parents (up to 20 weeks for birthing parents), and generous vacation policies to give employees time to recharge when needed. To build America’s energy future, we need everyone at the table. We are proud to be an equal opportunity employer, and encourage candidates from all backgrounds to apply to our open jobs. If you may require reasonable accommodations to participate in our interview process, please contact accommodations@formenergy.com. Requests for accommodations will be treated with discretion. Form Energy is committed to maintaining the privacy of our applicants. Please be aware that we will never solicit sensitive personal information such as Social Security numbers or bank account details during the recruiting or hiring process.", "summaryDescription" : "Senior Chemical Engineer at Form Energy", "createdAt" : "2026-06-16T00:32:09.832", "lastUpdated" : "2026-06-16T11:33:22.596", "ingestTimestamp" : "2026-06-16T00:32:09.832", "mongoId" : "6a30505ff292fd229ceefa31", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 111826, "salaryAnnualMax" : 139777, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 0.7777778, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Climate Tech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a305f10f292fd229cf77f0f", "title" : "Senior Chemical Engineer", "company" : "Form Energy", "industry" : "Research & Development", "salary" : { "min" : 111826.0, "max" : 139777.0, "currency" : "USD", "frequency" : "Yearly" }, "location" : "Berkeley, CA", "locations" : [ "Berkeley, CA" ], "timestamp" : "2026-06-16T10:38:24.350", "fingerprint" : "e58168ca87bb281442b9961978849cafa6e3a016af97023d590c6d31ee18176e", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/formenergy/2b1ae5b7-0a25-46bb-a09c-40db134ad53f/application", "externalId" : "2b1ae5b7-0a25-46bb-a09c-40db134ad53f", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Berkeley", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "37.8708393,-122.2728630" } ], "locationText" : "Berkeley, California, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "remoteFriendly" : false, "rawDescription" : "Are you ready to build America’s energy future? Form Energy is an American manufacturing and energy technology company. We’re revolutionizing energy storage with cost-effective, multi-day technology designed to keep the electric grid secure and reliable, even during extended periods of stress. By strengthening the electric system and reimagining what’s possible, we’re giving clean energy a whole new form! In recent years, Form Energy has earned a number of accolades, including being named by TIME as a “Best Invention”, MIT Technology Review as a “Top Climate Tech Company To Watch”, and Fast Company as “One of the Next Big Things In Tech”. We are making rapid progress on our mission of delivering energy storage for a better world, and our team is growing just as rapidly to meet demand. We have signed contracts with leading electric utilities across the United States and production of our iron-air batteries is underway at our first high-volume manufacturing facility in West Virginia. Working for Form Energy is more than just a job, it’s a chance to be part of something extraordinary. And now - right as we significantly scale up battery manufacturing - might be the most exciting moment in the company’s history to join. We are assembling a team of highly talented and driven individuals across the country. Driven by our core values of humanity, excellence, and creativity, our team is determined to deliver on our mission and transform the energy landscape for the better. Feeling energized to make a meaningful impact on the world? Then keep reading - you’ve come to the right place. ROLE DESCRIPTION Form Energy is hiring a Senior Chemical Engineer to join the Product Echem Performance team. In this role, you will build on existing results to improve our electrolyte product integration process and help optimize the electrolyte workflow for Form Energy's long-duration energy storage system. As a Senior Chemical Engineer specializing in fluid mechanics, handling systems, and mathematical modeling, you will play a key role in developing and owning predictive models for our iron-air battery — including a shunt current model and an electrolyte level model — as well as designing and developing test vehicle components. Your responsibilities will also include leading the analysis and definition of requirements for fluid and material management, with modeling as a core tool for driving design decisions. This role is crucial in conducting hands-on verification testing to ensure that our fluid handling systems meet all requirements, and in closing gaps between model predictions and real-world test data. This role offers the chance to also work closely with chemical, materials, and mechanical engineers on the technology development team in the lab and to analyze their data. This is an exciting opportunity to help shape and be part of the growth of a fast-moving company with breakthrough technology and an incredible mission! Relocation assistance is available. 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Form Energy offers competitive salaries, stock options, and a holistic benefits package to ensure all employees have what they need to thrive while working here. When it comes to you and your family’s health, we cover 100% of medical, dental, and vision premiums for full-time employees - and 80% of healthcare premiums for dependents. This starts from day one. We also offer at least 12 weeks of paid leave for new parents (up to 20 weeks for birthing parents), and generous vacation policies to give employees time to recharge when needed. To build America’s energy future, we need everyone at the table. We are proud to be an equal opportunity employer, and encourage candidates from all backgrounds to apply to our open jobs. If you may require reasonable accommodations to participate in our interview process, please contact accommodations@formenergy.com. Requests for accommodations will be treated with discretion. Form Energy is committed to maintaining the privacy of our applicants. Please be aware that we will never solicit sensitive personal information such as Social Security numbers or bank account details during the recruiting or hiring process.", "summaryDescription" : "Senior Chemical Engineer at Form Energy", "createdAt" : "2026-06-16T00:27:12.943", "lastUpdated" : "2026-06-16T10:38:24.350", "ingestTimestamp" : "2026-06-16T00:27:12.943", "mongoId" : "6a305f10f292fd229cf77f0f", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 111826, "salaryAnnualMax" : 139777, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 0.7777778, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Climate Tech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2c7b4474d8ee00a09490b1", "title" : "Senior Chemical / Process Engineer", "company" : "CycloKinetics", "salary" : { "min" : 135000.0, "max" : 185000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Chemical / Process Engineer in Salt Lake City, adjusted for the climate tech industry and full-time employment." }, "location" : "CycloKinetics - CK1", "locations" : [ "CycloKinetics - CK1" ], "timestamp" : "2026-06-16T01:12:58.018", "fingerprint" : "63cc493306f81384833110e93bf28bebbfd9d180c2f7ef6660845c42838f0221", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/cyclokinetics/jobs/5228231008", "externalId" : "5228231008", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Salt Lake City", "state" : "Utah", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7596198,-111.8867970" } ], "locationText" : "Salt Lake City, Utah, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Chemical Engineering, Process Engineering, Process Simulation, P&ID, HAZOP, Scale-up, GMP, Aspen Plus, Batch processing, Continuous processing, Process control", "professionalSkills" : [ "Project management", "Process design", "Process optimization", "Process validation" ], "hardSkillsList" : [ "Process modeling", "Process design", "Process optimization", "Process validation", "HAZOP analysis", "Scale-up design" ], "hardSkills" : [ { "name" : "Process modeling", "level" : "intermediate" }, { "name" : "Process design", "level" : "intermediate" }, { "name" : "Process optimization", "level" : "intermediate" }, { "name" : "Process validation", "level" : "intermediate" }, { "name" : "HAZOP analysis", "level" : "intermediate" }, { "name" : "Scale-up design", "level" : "intermediate" } ], "majorSkills" : "Process Engineering, Process Design, Scale-up, GMP", "majorSkillsList" : [ "Process Engineering", "Process Design", "Scale-up", "GMP" ], "coreResponsibilities" : "Design and develop chemical processes, Create and review P&IDs, Conduct HAZOP studies, Manage process scale-up activities, Ensure processes comply with GMP, Optimize existing processes, Troubleshoot process issues, Develop process validation protocols, Collaborate with cross-functional teams", "teamCollaboration" : "Cross-functional teams", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "GMP environments; Batch processing; Continuous processing", "domainList" : [ "gmp-environments", "batch-processing", "continuous-processing" ], "domainSpecificKnowledge" : [ "GMP environments", "Batch processing", "Continuous processing" ], "toolProficiency" : [ "Process simulation software", "Aspen Plus", "P&ID software" ], "documentationSkills" : "P&ID development; Process validation protocols", "problemSolvingSkills" : "Process optimization; Troubleshooting", "qualificationsBasic" : "5+ years of experience, Bachelor's degree in Chemical Engineering or related field, Experience with process simulation software, Experience with P&ID development, Experience with HAZOP studies, Experience with scale-up processes, Experience with GMP environments", "qualificationsPreferred" : "Master's degree preferred, Experience with Aspen Plus, Experience with batch processing, Experience with continuous processing, Experience with process control systems, Experience with validation protocols", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "About CycloKinetics CycloKinetics, is advancing the next generation of high-performance propellants for aerospace and defense. Our highly innovative technology allows us to harness existing energy from biomass and convert it to superior performance fuels and propellants across aviation, aerospace, and defense applications. We are a team of engineers, scientists, and operators driven by performance, innovation, and national security impact focused on building scalable, domestic energy solutions that power the future of propulsion. CycloKinetics is based in Salt Lake City, Utah. Job Summary: We are seeking an experienced Senior Chemical / Process Engineer to serve as a key technical leader for continuous process development and implementation. This role will focus heavily on distillation systems, hydrogenation processes, continuous flow operations, and translating process intent into real-world industrial systems. In this highly cross functional role, the individual will work closely with the R able to present data for strategic decisions Demonstrated proficiency with common computer tools and web‑based applications Ability to work effectively in fast‑paced development environments Track record of teamwork with personal accountability, attention to detail, collaboration, and delivering results Highly detail‑oriented, proactive, self‑driven, and able to take initiative to achieve scientific and operational goals Candidates with biorefinery, petroleum, or chemical industry backgrounds strongly encouraged to apply Must be able to use a respirator per OSHA standards and pass respirator fit test (requires being clean‑shaven where respirator seals) Physical Demands: Frequent lifting and moving of items up to fifty (50) pounds*, bending, reaching above shoulder level, climbing stairs, pulling, prolonged standing or sitting may be required. Must have safe work habits and perform all duties in accordance with company safety policies. Personal protective equipment is provided by the company, and its use is mandatory. General: This position is based in Salt Lake City, Utah with work performed on-site. CycloKinetics is an At-Will, VEVRAA, Equal Employment Opportunity Employer, E-Verify, and Drug Free Workplace. Benefits: CycloKinetics offers a competitive compensation and benefits package (health, dental, vision, employee and dependent life coverage(s) and accidental death and dismemberment, short-term disability, long-term disability, flexible spending accounts, health savings account, 401k matching, PTO, holiday pay, parental leave, and bonus potential). EEO Statement: CycloKinetics is an Equal Opportunity Employer and embraces diversity in our employee population. We are excited to work with talented individuals from a wide range of backgrounds. All employment decisions at CycloKinetics are based on business needs, job requirements and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status or special disabled veteran, marital status, parental status, pregnancy, genetic information, or any other legally protected status. We’re looking for detail-oriented team members who pride themselves on solving problems while bringing positive energy and strong communication skills to the table. If this describes you, come join our team today and contribute to the success of our organization! FLSA Classification: Exempt", "summaryDescription" : "Senior Chemical / Process Engineer at CycloKinetics. Skills: Process Engineering, Process Design, Scale-up, GMP. Design and develop chemical processes. Create and review P&IDs", "postedDate" : "2026-06-14T21:29:46.619", "createdAt" : "2026-06-14T21:29:46.619", "lastUpdated" : "2026-06-16T01:12:58.018", "ingestTimestamp" : "2026-06-14T21:29:46.619", "mongoId" : "6a2c7b4474d8ee00a09490b1", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 135000, "salaryAnnualMax" : 185000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Process modeling", "Process design", "Process optimization", "Process validation", "HAZOP analysis", "Scale-up design", "Process Engineering", "Process Design", "Scale-up", "GMP", "Project management", "GMP environments", "Batch processing", "Continuous processing", "Process simulation software", "Aspen Plus", "P&ID software" ], "skillCount" : 17, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Climate Tech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a30693af292fd229cfc761e", "title" : "Technician - Microbiology", "company" : "AsureQuality", "industry" : "Food And Beverages", "salary" : { "min" : 52000.0, "max" : 65000.0, "currency" : "NZD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an Entry-level Technician - Microbiology in Christchurch, New Zealand, adjusted for the Food & Beverage industry." }, "location" : "Christchurch, Canterbury Region, New Zealand", "locations" : [ "Christchurch", "Canterbury Region", "New Zealand" ], "timestamp" : "2026-06-16T09:02:04.697", "fingerprint" : "61107e4c7f8cc8e6fc7b8256a84f79c30abc065f5692408fedc5348e1ebcd05b", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/AsureQuality/6000000001152190-technician-microbiology", "externalId" : "6000000001152190", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Christchurch", "state" : "Canterbury Region", "country" : "New Zealand", "continent" : "oc", "source" : "llm", "workMode" : "onsite", "geo" : "-35.1938353,174.2947014" } ], "locationText" : "Christchurch, Canterbury Region, New Zealand", "employmentType" : "FULL_TIME", "experienceMinYears" : 0, "experienceMaxYears" : 2, "experienceLevel" : "entry", "hardSkillsList" : [ "Microbiological analysis" ], "hardSkills" : [ { "name" : "Microbiological analysis", "level" : "intermediate" } ], "majorSkills" : "Microbiology", "majorSkillsList" : [ "Microbiology" ], "coreResponsibilities" : "Complete sample testing, Adhere to laboratory procedures, Adhere to regulatory procedures, Keep records up to date, Maintain work area, Participate in working safely, Contribute to improvement activities", "teamCollaboration" : "Day to day improvement activities", "domainKnowledge" : "Food safety; Food quality", "domainList" : [ "food-safety", "food-quality" ], "domainSpecificKnowledge" : [ "Food safety", "Food quality" ], "communicationSkills" : "Written communication; Verbal communication", "continuousLearning" : "Train on the job; Develop hands on skills", "specialRequirements" : "Flexibility to work overtime, Work overtime at short notice", "outcomesObjectives" : "Ensure products meet standards", "qualificationsBasic" : "Recent graduate, Experience in similar environment, Worked in Retail or Hospitality, Good hand and eye coordination, Ability to work under pressure, Excellent time management, Organisational skill, Clear communication (written and verbal)", "qualificationsPreferred" : "Passion for Microbiology as a career", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Everyday our experienced team of 1600+ people work alongside farmers, producers, and others throughout the food supply chain to help them uphold what Aotearoa stands for in food - a higher standard of quality and safety. We are passionate about our shared role as Kaitiaki Kai, guardians of food, and have a deep responsibility to do the right thing for food and the environments it comes from. We are committed to attracting, developing, and retaining great people, and supporting them to be the best they can be. We know diverse teams are stronger teams and we believe in fairness and opportunity for all. We are looking for a full time Technician to join our Microbiology Team based at our Christchurch Laboratory. Successful applicants will be responsible for carrying out Microbiological analysis on routine samples and ensure our customer's products meet the highest standards of quality and safety. Your key duties will involve: * Complete sample testing within the given turn-around-time (TAT) * Strictly adhere to all laboratory and regulatory quality assurance procedures * Ensure all relevant records are kept up to date at all times * Maintain a clean and tidy work area * Participate and contribute to working safely * Be actively involved in all the day to day improvement activities Our laboratory is open 7 days a week and flexibility to work overtime at short notice is ideal. The roster for this role is Sunday to Thursday. The successful applicant will be working a minimum of 40 hours per week. About you: We want to hear from motivated individuals who are keen team players with a passion for providing quality customer focus. Ideally you will have/be; * Recent graduate * Experience in a similar environment or worked in Retail or Hospitality * Passionate about Microbiology as a career * Good hand and eye co-ordination * Strong attention to detail * Ability to work under pressure * Excellent time management and organisational skill * Clear communication (both written and verbal) ## Qualifications BSc or Diploma majoring in Food Science or Microbiology. ## Additional Information This is an excellent opportunity to train on the job and develop hands on skills in a commercial testing laboratory. You will learn from the best and be able to pursue career aspirations at AsureQuality. Apply on line today! Helping Aotearoa shape a better food world - Join us today!", "summaryDescription" : "Technician - Microbiology at AsureQuality. Skills: Microbiology. Complete sample testing. Adhere to laboratory procedures", "postedDate" : "2026-06-14T21:45:08.000", "createdAt" : "2026-06-16T00:00:59.544", "lastUpdated" : "2026-06-16T09:02:04.697", "ingestTimestamp" : "2026-06-16T00:00:59.544", "mongoId" : "6a30693af292fd229cfc761e", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "50k-75k", "hasSalary" : false, "allSkills" : [ "Microbiological analysis", "Microbiology", "Food safety", "Food quality" ], "skillCount" : 4, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Entry", "dataQualityScore" : 1.0, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Food & Beverage", "llmIndustryConfidence" : 0.92 }, { "id" : "6a16291c58b93c861e95a071", "title" : "Mechanical/Chemical EIT/Coordinator", "industry" : "Manufacturing", "salary" : { "min" : 65000.0, "max" : 85000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level Mechanical/Chemical EIT/Coordinator in Ann Arbor, United States, adjusted for manufacturing industry and full-time employment." }, "location" : "United States-Michigan-Ann Arbor", "locations" : [ "United States-Michigan-Ann Arbor" ], "timestamp" : "2026-06-15T04:55:19.099", "fingerprint" : "ff89d2db1638968b7cdf7f23e10ed182adb9949be11e7a54e7c29266252f8a09", "source" : "taleo", "language" : "en", "applyUrl" : "https://hdr.taleo.net/careersection/ex/jobdetail.ftl?job=780119", "externalId" : "780119", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Ann Arbor", "state" : "Michigan", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.2813722,-83.7484616" } ], "locationText" : "Ann Arbor, Michigan, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "toolProficiency" : [ "Microsoft Office" ], "qualificationsBasic" : "Bachelor's degree in Engineering, Computer skills in Microsoft Office", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Required Qualifications Bachelor's degree in Engineering Computer skills in Microsoft Office An attitude and commitment to being an active participant of our employee-owned culture What We Believe HDR is our company. Together, we build on each other's life experiences and perspectives to make great things possible every day. This shapes our collaborative culture, encourages organizational trust and connects us closer to the clients and communities we serve. Our Commitment As employee owners, we all have a role in creating an inclusive environment where each of us is welcomed, valued, respected and empowered to bring our authentic selves to work every day. Our eight Employee Network Groups (Asian Pacific, Black, Hispanic/Latino(a), LGBTQ+, People with Disabilities, Veterans, Women, Young Professionals) help create a sense of belonging and foster a supportive environment where everyone is empowered to engage and contribute. Each group has an executive sponsor and is open to all employees. United States-Michigan-Ann Arbor", "summaryDescription" : "Mechanical/Chemical EIT/Coordinator", "createdAt" : "2026-06-14T04:58:24.098", "lastUpdated" : "2026-06-15T04:55:19.099", "ingestTimestamp" : "2026-06-14T04:58:24.098", "mongoId" : "6a16291c58b93c861e95a071", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 65000, "salaryAnnualMax" : 85000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Microsoft Office" ], "skillCount" : 1, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Entry", "dataQualityScore" : 0.6666667, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Manufacturing", "llmIndustryConfidence" : 0.9 }, { "id" : "6a305571f292fd229cf1f9c0", "title" : "Technical Officer (Chemical and Biomolecular Engineering)", "company" : "The University of Sydney", "industry" : "Education", "salary" : { "min" : 107.0, "max" : 107.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "Australia", "locations" : [ "Australia" ], "timestamp" : "2026-06-16T12:22:32.535", "fingerprint" : "853442d3a4bb8ae77d6b3dbddb4ec54fd01cf5bdeeb5979d531865f467278326", "source" : "workday", "language" : "en", "applyUrl" : "https://usyd.wd105.myworkdayjobs.com/USYD_EXTERNAL_CAREER_SITE/job/Darlington-Campus/Technical-Officer--Chemical-and-Biomolecular-Engineering-_0152371-2", "externalId" : "0152371", "industryFunction" : { }, "locationPoint" : "-25.2744,133.7751", "structuredLocations" : [ { "country" : "Australia", "continent" : "oc", "workMode" : "remote" } ], "locationText" : "Australia", "employmentType" : "FULL_TIME", "technicalSkills" : "Chemical engineering, Biomolecular engineering", "professionalSkills" : [ "Technical services", "Research support", "Teaching support", "Laboratory equipment maintenance", "Inventory management", "Safety documentation development", "WHS compliance", "Process control", "Industrial chemical engineering", "Electronics", "Additive manufacturing", "Machining", "CAD" ], "hardSkillsList" : [ "Equipment operation", "Procedure preparation", "Safety compliance" ], "softSkillsList" : [ "Problem solving", "Relationship building" ], "hardSkills" : [ { "name" : "Equipment operation", "level" : "intermediate" }, { "name" : "Procedure preparation", "level" : "intermediate" }, { "name" : "Safety compliance", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Problem solving" }, { "name" : "Relationship building" } ], "majorSkills" : "Technical support, Laboratory operations, WHS compliance", "majorSkillsList" : [ "Technical support", "Laboratory operations", "WHS compliance" ], "coreResponsibilities" : "Deliver technical support, Deliver technical services, Tailor services to user requirements, Escalate service gaps, Escalate feedback, Support effective resource utilisation, Meet education requirements, Meet research requirements, Adhere to WHS procedures, Maintain professionalism, Support teaching operations, Deliver training to facility users, Induct facility users, Perform general laboratory procedures, Contribute to team culture, Collaborate with technical support teams, Support central project operations, Set up laboratory equipment, Operate laboratory equipment, Prepare operating procedures, Assist with process implementation, Assist with system implementation, Assist with new ways of working, Improve efficiency, Improve service delivery, Provide hands-on support for research, Provide hands-on support for teaching, Provide hands-on support for demonstrations, Maintain laboratory equipment, Manage inventories, Provide guidance to staff, Provide guidance to students, Provide training for staff, Provide training for students, Contribute to safety documentation, Ensure compliance with WHS standards, Resolve issues impacting research operations", "teamCollaboration" : "Work independently; Work collaboratively within team; Collaborate with other technical teams; Collaborate with University departments", "domainKnowledge" : "Chemical engineering; Biomolecular engineering; Hazardous substances; Compressed gases; Cryogens; Biological substances", "domainList" : [ "chemical-engineering", "biomolecular-engineering", "hazardous-substances", "compressed-gases", "cryogens", "biological-substances" ], "domainSpecificKnowledge" : [ "Chemical engineering", "Biomolecular engineering", "Hazardous substances", "Compressed gases", "Cryogens", "Biological substances" ], "communicationSkills" : "Customer-facing communications", "documentationSkills" : "Safety documentation", "innovationCreativity" : "Enable innovative teaching; Enable innovative research", "problemSolvingSkills" : "Problem solving", "specialRequirements" : "Full strength and range of movement, Flexible joints, Lift, carry, push, pull, Manipulate items, Tolerate repetitive physical tasks", "outcomesObjectives" : "Strengthen education support outcomes; Enhance research support outcomes; Improve efficiency; Improve service delivery", "qualificationsBasic" : "Bachelor's degree in chemical engineering or related field, Relevant training and experience, Experience providing technical support, Experience providing training, Experience providing routine maintenance on chemical engineering equipment, Experience providing routine maintenance on laboratory equipment, Experience engaging with external parties, Experience coordinating repair of equipment, Experience coordinating procurement of equipment, Experience in safe handling of biological substances, Experience in safe handling of hazardous substances, Experience in safe storage of biological substances, Experience in safe storage of hazardous substances, Experience in safe disposal of biological substances, Experience in safe disposal of hazardous substances, Experience adhering to WHS compliance, Experience improving WHS compliance, Full strength and range of movement in both arms, Flexible joints to lift, carry, push, pull, Ability to manipulate items, Tolerate repetitive physical tasks, Unrestricted work rights in Australia", "qualificationsPreferred" : "Experience or qualification in process control, Experience or qualification in industrial chemical engineering, Experience or qualification in WHS compliance, Experience or qualification in electronics, Experience or qualification in additive manufacturing, Experience or qualification in machining, Experience or qualification in CAD", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "* **Full time, fixed term position until 30th October 2026. Located at the Electrical Engineering Building (J03) on the Darlington Campus** * **Deliver hands-on support for research operations, teaching activities, and outreach demonstrations** * **Base Salary HEO6 $107,12 - $115,686 + 17% superannuation** **About the opportunity** The University of Sydney is welcoming applications for motivated and experienced **Technical Officer (****Chemical and Biomolecular Engineering)** to join the Central Operations Services (COS) Engineering Delivery Team and provide high-quality technical services within the designated area of responsibility to strengthen and enhance education and research support outcomes. The **Technical Officer** (**Chemical and Biomolecular Engineering)** will work independently and collaboratively within the team to contribute high quality technical services that support teaching and research activities within the designated areas of responsibility. This role involves delivering hands on assistance for practical classes, demonstrations, and research operations, maintaining and operating laboratory equipment and managing inventories. The **Technical Officer** will also provide guidance and training for staff and students, contribute to the development of safety documentation, and ensure compliance with Work Health and Safety standards in alignment with University policies and legislation. The position requires strong problem solving and communication skills to manage the delivery of technical support and resolve issues impacting the research operations of academic staff and students. You will be responsible for setting up and operating complex or bespoke laboratory equipment, preparing operating procedures, and assisting with the implementation of new processes, systems, and ways of working to improve efficiency and service delivery. Collaboration with other technical teams and University departments will be essential to support resource sharing and consistent practices. This is an opportunity to play a key role in enabling innovative teaching and research in a safe and well managed environment. Your key responsibilities will be to: * deliver technical support and services in accordance with the role and tailor services to user/client requirements within remit and escalate service gaps/feedback as appropriate * support the effective utilisation of resources within the designated area of responsibility, ensuring that the work area’s education/research requirements are effectively met * lead by example by demonstrating a strong adherence to established WHS and compliance procedures, and maintain professionalism in all customer-facing activities and communications * support teaching operations and deliver training to facility users in the safe operation of equipment, building inductions, and general laboratory procedures * contribute to a positive, professional and customer focused team culture * collaborate with other technical support teams across the university and support the operations of projects managed centrally as required. **About you** * bachelor's degree in chemical engineering or in a related field or relevant training and experience * experience in providing technical support, training, and routine maintenance on common chemical engineering or laboratory equipment in a research or teaching laboratory environment * experience engaging with external parties or contractors to coordinate repair or procurement of equipment to maintain research continuity * experience in the safe handling/storage/disposal of biological and hazardous substances (e.g., chemicals, waste, compressed gases and cryogens) and relevant experience in adhering to and improving WHS compliance in modern laboratory environments * strong communication and relationship building skills, with an ability to establish and maintain working relationships with customers * full strength and range of movement in both arms and flexible joints to lift, carry, push, pull a variety of loads; ability to manipulate items and tolerate repetitive physical tasks * possess experience or qualification in process control, industrial chemical engineering and WHS compliance or other relevant practical engineering skills (electronics, additive manufacturing, machining, CAD) (desirable). **Sponsorship / work rights for** **Australia** You must have unrestricted work rights in Australia for the duration of this employment to be eligible to apply. Visa sponsorship is not available for this appointment. **Pre-employment checks** Your employment is conditional upon the successful completion of all pre-employment or background checks required for the role in terms satisfactory to the University. Also, to meet the University’s obligations under the National Higher Education Code to [Prevent and Eliminate Gender-Based Violence](https://www.sydney.edu.au/about-us/vision-and-values/safety-and-respect/sexual-harm-and-gender-based-violence.html) you will be asked to declare if you have been investigated for, or found to engaged in, sexual harm or gender-based violence in the course of previous employment or in a legal process. Similarly, your ongoing employment is conditional upon the satisfactory maintenance of all relevant clearances and background check requirements. If you do not meet these conditions, the University may take any necessary step, including the termination of your employment. **EEO statement** At the University of Sydney, our shared values are [trust, accountability and excellence](https://www.sydney.edu.au/about-us/vision-and-values.html) and we strive to be a place where everyone can thrive. We are committed to creating a University community that thrives through diversity and reflects the wider community that we serve. We deliver on this through our commitment to [diversity and inclusion](https://www.sydney.edu.au/about-us/vision-and-values/diversity.html), evidenced by our people and culture programs, as well as key strategies to increase participation and support the careers of [Aboriginal and Torres Strait Islander People](https://www.sydney.edu.au/about-us/careers-at-sydney/indigenous-careers.html), [women](https://www.sydney.edu.au/about-us/vision-and-values/diversity/gender-equity.html), [people living with a disability](https://www.sydney.edu.au/about-us/careers-at-sydney/careers-for-people-with-disability.html), [people from culturally and linguistically diverse backgrounds](https://www.sydney.edu.au/about-us/vision-and-values/diversity/cultural-diversity.html), and those who identify as [LGBTQIA+](https://www.sydney.edu.au/about-us/vision-and-values/diversity/lgbtiq-community.html). We welcome applications from candidates from all backgrounds. We are proud to be recognised as an Australian Workplace Equality Index (AWEI) Platinum Employer. [Find out more about our work on diversity and inclusion](http://sydney.edu.au/about-us/vision-and-values/diversity.html). **How to apply** Applications (including a cover letter, CV, and any additional supporting documentation) can be submitted via the **Apply** button at the top of the page. For employees of the University or contingent workers, please login into your [**Workday**](https://sydney.edu.au/workday) account and navigate to the Career icon on your Dashboard. Click on USYD Find Jobs and apply. For a confidential discussion about the role, or if you require reasonable adjustment or any documents in alternate formats, please contact Kevin Lim, Recruitment Operations by email to [kevin.lim@sydney.edu.au](mailto:kevin.lim@sydney.edu.au). **©** The University of Sydney The University reserves the right not to proceed with any appointment. Click to view the [Position Description](https://unisyd.sharepoint.com/:b:/s/WorkdayIntegration/IQAMFtUXkONXRrlfePHNQ8AqAR5Z9jDUv3SdCaqyf7uyYQs?download=1) for this role. **Applications Close** Monday 29 June 2026 11:59 PM", "summaryDescription" : "Technical Officer (Chemical and Biomolecular Engineering) at The University of Sydney. Skills: Technical support, Laboratory operations, WHS compliance. Deliver technical support. Deliver technical services", "postedDate" : "2026-06-16T03:44:04.607", "createdAt" : "2026-06-16T03:44:04.600", "lastUpdated" : "2026-06-16T12:22:32.535", "ingestTimestamp" : "2026-06-16T03:44:04.600", "mongoId" : "6a305571f292fd229cf1f9c0", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://usyd.wd105.myworkdayjobs.com/USYD_EXTERNAL_CAREER_SITE/job/Darlington-Campus/Technical-Officer--Chemical-and-Biomolecular-Engineering-_0152371-2", "salaryAnnualMin" : 222560, "salaryAnnualMax" : 222560, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Equipment operation", "Procedure preparation", "Safety compliance", "Problem solving", "Relationship building", "Technical support", "Laboratory operations", "WHS compliance", "Technical services", "Research support", "Teaching support", "Laboratory equipment maintenance", "Inventory management", "Safety documentation development", "Process control", "Industrial chemical engineering", "Electronics", "Additive manufacturing", "Machining", "CAD", "Chemical engineering", "Biomolecular engineering", "Hazardous substances", "Compressed gases", "Cryogens", "Biological substances" ], "skillCount" : 26, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Education", "llmIndustryConfidence" : 0.95 }, { "id" : "6a191e7758b93c861e39f686", "title" : "Product Manager – Chemical Product Mgmt.", "company" : "Mercedes-Benz Research and Development India", "industry" : "Manufacturing", "salary" : { "min" : 1850000.0, "max" : 2750000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Product Manager in Bangalore, India, adjusted for mid-seniority and the automotive industry." }, "location" : "India-Karnataka-Bangalore", "locations" : [ "India-Karnataka-Bangalore", "'Embassy Crest' Plot No 5, , EPIP Zone, Phase 1, " ], "timestamp" : "2026-06-15T06:48:39.258", "fingerprint" : "08f7b20469ff8a8e1883ae8d046cd1e4b3cf95404aa001cd029021e78ce2838a", "source" : "taleo", "language" : "en", "applyUrl" : "https://tas-daimler.taleo.net/careersection/ex/jobdetail.ftl?job=883006", "externalId" : "883006", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Bangalore", "state" : "Karnataka", "country" : "India", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "12.9767936,77.5900820" } ], "locationText" : "Bangalore, Karnataka, India", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 5, "experienceMaxYears" : 8, "experienceLevel" : "Mid", "professionalSkills" : [ "Product lifecycle management", "Portfolio management", "Commercial acumen", "Cost optimization", "Pricing strategies", "Tender participation", "Commercial negotiations", "Supplier management", "Stakeholder management", "Cross-functional collaboration", "Problem-solving skills" ], "hardSkillsList" : [ "Chemical products understanding", "Formulations understanding" ], "softSkillsList" : [ "Presentation skills" ], "hardSkills" : [ { "name" : "Chemical products understanding", "level" : "intermediate" }, { "name" : "Formulations understanding", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Presentation skills" } ], "majorSkills" : "Product strategy, Roadmap development, User stories, Cross-functional collaboration", "majorSkillsList" : [ "Product strategy", "Roadmap development", "User stories", "Cross-functional collaboration" ], "coreResponsibilities" : "Own product roadmap, Manage product lifecycle, Define product positioning, Drive new product introductions, Manage product portfolio performance, Identify portfolio expansion opportunities, Support pricing strategies, Support tender participation, Support commercial negotiations, Collaborate with suppliers, Lead supplier alignment, Act as primary interface, Improve product management processes, Mitigate supply risks, Mitigate quality risks, Mitigate regulatory risks, Support automation initiatives, Support data-driven reporting", "teamCollaboration" : "Cross-functional collaboration; Collaborate with suppliers; Collaborate with procurement; Collaborate with R&D; Collaborate with quality; Collaborate with logistics", "projectManagementSkills" : [ "Roadmap", "New product introductions" ], "domainKnowledge" : "Chemical products; Regulatory frameworks; Car care chemicals; Workshop chemicals; Oils; Greases; Aerosols; Adhesives; Consumables", "domainList" : [ "chemical-products", "regulatory-frameworks", "car-care-chemicals", "workshop-chemicals", "oils", "greases", "aerosols", "adhesives", "consumables" ], "domainSpecificKnowledge" : [ "Chemical products", "Regulatory frameworks", "Car care chemicals", "Workshop chemicals", "Oils", "Greases", "Aerosols", "Adhesives", "Consumables" ], "communicationSkills" : "Presentation skills", "continuousLearning" : "Continuous learning opportunities", "innovationCreativity" : "Drive innovation", "problemSolvingSkills" : "Problem-solving skills", "outcomesObjectives" : "Revenue growth; Margin growth; On-time product launches; Compliant product launches; Portfolio optimization; Cost savings achieved; Stakeholder satisfaction; Operational efficiency improvements", "qualificationsBasic" : "Bachelor's degree in Chemistry, 5–8 years of experience in product management", "qualificationsPreferred" : "MBA preferred, Experience in chemicals, Experience in automotive, Experience in FMCG, Experience in industrial products, Experience with global suppliers, Experience with multi-market portfolios", "remoteFriendly" : false, "rawDescription" : "About MBRDI Mercedes-Benz Research and Development India (MBRDI), headquartered in Bengaluru with a satellite office in Pune, is the largest R&D center for Mercedes-Benz Group AG outside of Germany. Our mission is to drive innovation and excellence in automotive engineering, digitalization, and sustainable mobility solutions, shaping the future of mobility. Role Summary The Product Manager – Chemical Product Management is responsible for the end-to-end lifecycle management of chemical products, including car care chemicals, workshop chemicals, oils, greases, aerosols, adhesives, and related consumables. The role focuses on portfolio strategy, product performance, compliance, supplier management, cost optimization, and revenue growth across regional and global markets. Key Responsibilities Product Strategy & Lifecycle Management Own the product roadmap and lifecycle (concept, launch, optimization, phase-out) for assigned chemical product categories. Define product positioning, value propositions, and differentiation aligned with business and market needs. Drive new product introductions (NPI), replacements, and localization initiatives. Portfolio & Commercial Management Manage product portfolio performance (revenue, margin, volume, cost, and market share). Identify opportunities to expand the portfolio, optimize SKUs, and improve profitability. Support pricing strategies, tender participation, and commercial negotiations. Supplier & Stakeholder Management Collaborate with suppliers, procurement, R&D, quality, and logistics teams. Lead supplier alignment on specifications, formulations, packaging, labeling, and timelines. Act as the primary interface between internal stakeholders and external partners. Process & Operations Excellence Improve and standardize product management processes to ensure on-time launches. Identify and mitigate risks related to supply, quality, and regulatory changes. Support automation, data-driven reporting, and continuous improvement initiatives. Key Skills & Competencies Strong understanding of chemical products, formulations (good to have), and regulatory frameworks. Product lifecycle and portfolio management expertise. Commercial acumen with experience in pricing, tenders, and cost optimization. Stakeholder management and cross-functional collaboration. Analytical mindset with strong problem-solving skills. Excellent communication and presentation skills. Success Metrics Revenue and margin growth of the chemical product portfolio. On-time and compliant product launches. Portfolio optimization and cost savings achieved. Stakeholder satisfaction and operational efficiency improvements. Qualifications & Experience Bachelor’s degree in Chemistry, Chemical Engineering, or a related field (MBA preferred). 5–8 years of experience in product management, preferably in chemicals, automotive, FMCG, or industrial products. Experience working with global suppliers and multi-market portfolios. Why Join Us? · Be part of a purpose-driven organization that is shaping the future of mobility · Work on cutting-edge technologies and global projects · Thrive in a collaborative, diverse, and inclusive environment · Access world-class infrastructure and continuous learning opportunities Equal Opportunity Statement At MBRDI, we are committed to diversity and inclusion. We welcome applications from all qualified individuals, regardless of gender, background, or ability. Mercedes-Benz Research and Development India Private Limited", "summaryDescription" : "Product Manager – Chemical Product Mgmt. at Mercedes-Benz Research and Development India. Skills: Product strategy, Roadmap development, User stories, Cross-functional collaboration. Own product roadmap. 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Supplier alignment; Internal stakeholders; External partners", "projectManagementSkills" : [ "Roadmap", "New product introductions" ], "domainKnowledge" : "Chemical products; Regulatory frameworks; Car care chemicals; Workshop chemicals; Oils; Greases; Aerosols; Adhesives; Consumables", "domainList" : [ "chemical-products", "regulatory-frameworks", "car-care-chemicals", "workshop-chemicals", "oils", "greases", "aerosols", "adhesives", "consumables" ], "domainSpecificKnowledge" : [ "Chemical products", "Regulatory frameworks", "Car care chemicals", "Workshop chemicals", "Oils", "Greases", "Aerosols", "Adhesives", "Consumables" ], "communicationSkills" : "Presentation skills", "continuousLearning" : "Continuous learning opportunities", "innovationCreativity" : "Drive innovation", "problemSolvingSkills" : "Problem-solving skills; Analytical mindset", "outcomesObjectives" : "Revenue growth; Margin growth; On-time product launches; Compliant product launches; Portfolio optimization; Cost savings achieved; Stakeholder satisfaction; Operational efficiency improvements", "qualificationsBasic" : "Bachelor's degree in Chemistry, 5–8 years of experience in product management", "qualificationsPreferred" : "MBA preferred, Experience in chemicals, Experience in automotive, Experience in FMCG, Experience in industrial products, Experience with global suppliers, Experience with multi-market portfolios", "remoteFriendly" : false, "rawDescription" : "About MBRDI Mercedes-Benz Research and Development India (MBRDI), headquartered in Bengaluru with a satellite office in Pune, is the largest R&D center for Mercedes-Benz Group AG outside of Germany. Our mission is to drive innovation and excellence in automotive engineering, digitalization, and sustainable mobility solutions, shaping the future of mobility. Role Summary The Product Manager – Chemical Product Management is responsible for the end-to-end lifecycle management of chemical products, including car care chemicals, workshop chemicals, oils, greases, aerosols, adhesives, and related consumables. The role focuses on portfolio strategy, product performance, compliance, supplier management, cost optimization, and revenue growth across regional and global markets. Key Responsibilities Product Strategy & Lifecycle Management Own the product roadmap and lifecycle (concept, launch, optimization, phase-out) for assigned chemical product categories. Define product positioning, value propositions, and differentiation aligned with business and market needs. Drive new product introductions (NPI), replacements, and localization initiatives. Portfolio & Commercial Management Manage product portfolio performance (revenue, margin, volume, cost, and market share). Identify opportunities to expand the portfolio, optimize SKUs, and improve profitability. Support pricing strategies, tender participation, and commercial negotiations. Supplier & Stakeholder Management Collaborate with suppliers, procurement, R&D, quality, and logistics teams. Lead supplier alignment on specifications, formulations, packaging, labeling, and timelines. Act as the primary interface between internal stakeholders and external partners. Process & Operations Excellence Improve and standardize product management processes to ensure on-time launches. Identify and mitigate risks related to supply, quality, and regulatory changes. Support automation, data-driven reporting, and continuous improvement initiatives. Key Skills & Competencies Strong understanding of chemical products, formulations (good to have), and regulatory frameworks. Product lifecycle and portfolio management expertise. Commercial acumen with experience in pricing, tenders, and cost optimization. Stakeholder management and cross-functional collaboration. Analytical mindset with strong problem-solving skills. Excellent communication and presentation skills. Success Metrics Revenue and margin growth of the chemical product portfolio. On-time and compliant product launches. Portfolio optimization and cost savings achieved. Stakeholder satisfaction and operational efficiency improvements. Qualifications & Experience Bachelor’s degree in Chemistry, Chemical Engineering, or a related field (MBA preferred). 5–8 years of experience in product management, preferably in chemicals, automotive, FMCG, or industrial products. Experience working with global suppliers and multi-market portfolios. Why Join Us? · Be part of a purpose-driven organization that is shaping the future of mobility · Work on cutting-edge technologies and global projects · Thrive in a collaborative, diverse, and inclusive environment · Access world-class infrastructure and continuous learning opportunities Equal Opportunity Statement At MBRDI, we are committed to diversity and inclusion. We welcome applications from all qualified individuals, regardless of gender, background, or ability. Mercedes-Benz Research and Development India Private Limited", "summaryDescription" : "Product Manager – Chemical Product Mgmt. at Mercedes-Benz Research and Development India. Skills: Product strategy, Roadmap development, User stories, Cross-functional collaboration. Own product roadmap. Manage product lifecycle", "createdAt" : "2026-06-14T06:41:29.004", "lastUpdated" : "2026-06-15T05:01:45.330", "ingestTimestamp" : "2026-06-14T06:41:29.004", "mongoId" : "69ce5e3b9bc74574cb6779a2", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Chemical products understanding", "Formulations knowledge", "Presentation skills", "Product strategy", "Roadmap development", "User stories", "Cross-functional collaboration", "Product lifecycle management", "Portfolio management", "Commercial acumen", "Cost optimization", "Stakeholder management", "Problem-solving skills", "Roadmap", "New product introductions", "Chemical products", "Regulatory frameworks", "Car care chemicals", "Workshop chemicals", "Oils", "Greases", "Aerosols", "Adhesives", "Consumables" ], "skillCount" : 24, "jobCategory" : "product", "jobSubcategory" : "product_management", "seniorityLevel" : "Mid", "dataQualityScore" : 0.8888889, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Automotive", "llmIndustryConfidence" : 0.95 }, { "id" : "6a3055a1f292fd229cf20678", "title" : "Chemical Production Operator", "company" : "Huntsman", "industry" : "Manufacturing", "salary" : { "min" : 35000.0, "max" : 50000.0, "currency" : "GBP", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Chemical Production Operator in the United Kingdom, adjusted for industry and company size." }, "location" : "United Kingdom", "locations" : [ "United Kingdom" ], "certifications" : [ "Forklift Licence" ], "timestamp" : "2026-06-16T15:04:39.354", "fingerprint" : "c6e6a727569e1563d2eb69e62fb07b081bc0cf3c331d52b022bd3628088fb296", "source" : "workday", "language" : "en", "applyUrl" : "https://huntsman.wd1.myworkdayjobs.com/Huntsman/job/UK---Duxford/Chemical-Production-Operator_J-019921", "externalId" : "J-019921", "industryFunction" : { }, "locationPoint" : "55.3781,-3.436", "structuredLocations" : [ { "country" : "United Kingdom", "continent" : "eu", "workMode" : "onsite" } ], "locationText" : "United Kingdom", "employmentType" : "FULL_TIME", "hardSkillsList" : [ "Manual handling", "Lifting" ], "hardSkills" : [ { "name" : "Manual handling", "level" : "intermediate" }, { "name" : "Lifting", "level" : "intermediate" } ], "majorSkills" : "Process operation, Chemical manufacturing", "majorSkillsList" : [ "Process operation", "Chemical manufacturing" ], "coreResponsibilities" : "Operate plant machinery, Manufacture products, Fill products, Pack products, Report near misses, Report incidents, Report accidents, Investigate incidents, Investigate accidents, Set up batches, Check batches, Weigh batches, Add materials, Move batch materials, Complete documentation, Provide handover, Clean vessels, Clean machinery, Ensure targets are met, Maintain quality standards, Maximize efficiency, Report maintenance work, Keep workstation clean, Keep workstation tidy, Keep workstation organised", "teamCollaboration" : "Work as part of team", "domainKnowledge" : "Chemical processes; High-performance adhesives", "domainList" : [ "chemical-processes", "high-performance-adhesives" ], "domainSpecificKnowledge" : [ "Chemical processes", "High-performance adhesives" ], "documentationSkills" : "Complete documentation", "continuousLearning" : "Training costs covered; Sitewide learning days; E-learning courses; EHS courses; Job related courses", "innovationCreativity" : "Identify areas for improvement; Identify cost savings", "problemSolvingSkills" : "Minimize downtime; Minimize cost", "specialRequirements" : "Physically demanding role, Manual handling, Ability to carry/lift", "outcomesObjectives" : "Maximize production output; Minimize downtime; Minimize cost", "qualificationsBasic" : "GCSE Maths and English, Computer literate, Awareness of Health & Safety", "qualificationsPreferred" : "Chemistry or technical qualification, Experience in manufacturing process environment, Experience in chemical industry, Forklift Licence or capacity to learn", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Job Description** : **Contract:** Permanent **Shift:** 40 hours, weekly rotations (6am – 2pm, 2pm – 10pm, 10pm-2pm Monday to Friday) Huntsman are recruiting permanent Production Operators for our chemical manufacturing site in Duxford, Cambridge. As a flexible and motivated team member, you will work a three-shift system, 40 hours a week, operating plant equipment and chemical processes safely and efficiently to maximize production output. You will be trained to use a wide range of processing equipment, varying from planetary mixers to reaction vessels, to manufacture our high-performance adhesives. **As Chemical Production Operator, you will:** * Operate plant machinery to manufacture, fill and pack products following standard operating procedures and in a safe and efficient manner * Ensure all work is carried out safely and all near misses, incidents and accidents are reported/investigated. * Setting up batches, checking, weighing and adding materials, and physically moving batch materials where required. * Complete all related documentation accurately and provide suitable handover to on-coming shifts. * Clean vessels and machinery between campaigns to ensure no cross-contamination of product and/or materials to subsequent batches. * Work as part of a team to ensure targets are met whilst maintaining quality standards and maximising efficiency. * Report plant maintenance work requirements to minimise downtime and cost. * Keep workstation clean, tidy and organised in line with the 5S approach. * Identify areas for improvement and/or cost savings. **Skills & Experience Required:** * Strong attention to detail. * Strong numerical ability with GCSE Maths and English. Chemistry or a technical qualification is advantageous. * Experience in a manufacturing process environment is preferred, or with experience in the chemical industry. * Forklift Licence or the capacity to learn. * Excellent, reliable team worker, able to adapt to changing priorities. * Computer literate. * This role is physically demanding requiring a certain amount of manual handling and ability to carry/lift variety of items. * Awareness and understanding of Health & Safety. Working Hours: Monday – Friday, 8-hour shifts. 6am-2pm, 2pm – 10pm, 10- 6am for which you will receive a shift premium. **What we offer:** * Financial Reward: Competitive salary, pension scheme, a guaranteed annual payment, non-contractual Incentive Compensation Scheme, free onsite parking. * Health and Wellbeing: Private health insurance & employee assistance programmes offering access to online GP, mental health support and physiotherapy, Cycle to work scheme, free fruit, a day off for your birthday. * Family and Caregiving: Enhanced pay for maternity, paternity and adoption and shared parental leave. * Training: Training costs covered by the company, sitewide learning days, unlimited access to 10,000+ e-learning courses as well as other EHS and job related courses. **About Huntsman:** At Huntsman, we welcome talent, experience, and fresh ideas from all employees at all stages of their careers. As an integral part of a dynamic, industry-leading company, you will have the opportunity to make a difference and be part of a family-like atmosphere. We prioritize safety and ethics, and in return, we offer competitive compensation and benefits packages. To learn more about Huntsman and our chemical products, please visit our website at [www.huntsman.com](http://www.huntsman.com/). **Additional Locations:**", "summaryDescription" : "Chemical Production Operator at Huntsman. Skills: Process operation, Chemical manufacturing. Operate plant machinery. 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PQ’s products are used in a wide variety of industrial processes and many customer products, from decorative paints to green cement, from clean drinking water to green tires and from toothpaste to biofuels and beer. Ideal candidates resonate with PQ’s Core Values of Integrity, Sustainability, People, Customer Focus and Safety. Successful employees embrace and model these values in their behaviors and actions. This position applies to the overall operation of the liquid sodium silicate dissolving plant, and potassium silicate dissolving plant. It has the responsibility of maintaining maximum safety, efficiency, reliability, productivity, quality, and customer service. Duration 6 -12 months. * Off load railcars. * Load trucks for delivering products to the customer. * Perform routine equipment inspections. * Perform uninterrupted glass dissolving production. * Perform minor equipment repair. * Maintain work area clean and free from all safety hazards. * Assist in plant budget development. * Perform efficient start up/shut-down of plant and related equipment. * Maintain active participation in ISO audits/EHS audits/environmental audits. * Perform all quality checks on products shipped, boiler water and maintain records. * Obtain knowledge of all company policies/plant procedures/ISO procedures/Emergency Response Plan. * Prioritize in emergency situations and provide communication to proper authorities. * Hold a 5th class Power Engineer’s (boiler operator’s) ticket. * Possess good math, reading, writing and computer skills. * Other duties as assigned by the Unit Manager. ## Qualifications * Boiler Ticket preferred * Minimun 2 years of experience in manufacutirng environamen * Exceptional communication skills, both verbal and written. * Ability to learn and comprehend manufacturing processes. * Ability to work as a member of a 3 person team. * Willingness to learn new skills, as needed. * Ability to assist others in completing required tasks. * Work safely and abide by all safety rules and requirements. ## Additional Information EHS Responsibilities * Communicates, promotes and personally demonstrates Safety/Health (including PQP Principles) as #1 priority * Participation in risk assessment audits as applicable * Understand PQ Principles (PQP) and how they are implemented in the site organization, rules and procedures * Completes HSE training requirements identified for the job in a timely manner National Silicates Partnership is an equal employment opportunity employer. Accordingly, reasonable accommodations are available upon request for candidates taking part in relation to the materials or processes we use in the recruitment process.", "summaryDescription" : "Chemical Plant Operator (Contract) at National Silicate Partnership", "postedDate" : "2026-06-12T17:16:28.000", "createdAt" : "2026-06-14T09:23:01.876", "lastUpdated" : "2026-06-15T08:44:56.293", "ingestTimestamp" : "2026-06-14T09:23:01.876", "mongoId" : "6a2c85e674d8ee00a096635b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Liquid sodium silicate plant", "Potassium silicate plant", "ISO procedures", "Emergency Response Plan", "PQ Principles", "5th class Power Engineer’s ticket" ], "skillCount" : 6, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Manufacturing", "llmIndustryConfidence" : 0.95 }, { "id" : "6a26203374d8ee00a01fbee3", "title" : "Senior Analyst, Microbiology and Lab, Biologics", "company" : "Roche", "industry" : "Healthcare", "salary" : { "min" : 350000.0, "max" : 550000.0, "currency" : "CNY", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Senior Analyst in Microbiology and Lab at a large biotech company in Shanghai, China, adjusted for seniority and industry." }, "location" : "Shanghai", "locations" : [ "Shanghai", "China" ], "timestamp" : "2026-06-12T17:34:53.276", "fingerprint" : "7579d29de90e3a92c5724c40c2ad6bf3bb54be0093cab01355df4e259091e1b7", "source" : "workday", "language" : "en", "applyUrl" : "https://roche.wd3.myworkdayjobs.com/roche-ext/job/Shanghai/Senior-Analyst--Microbiology-and-EM-Lab--Biologics_202604-110281", "externalId" : "202604-110281", "industryFunction" : { }, "locationPoint" : "31.22222,121.45806", "structuredLocations" : [ { "city" : "Shanghai", "country" : "China", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "31.2312707,121.4700152" } ], "locationText" : "Shanghai, China", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's Degree", "experienceMinYears" : 2, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Microbiological testing", "Aseptic assurance", "Quality control procedures", "Laboratory operations" ], "hardSkillsList" : [ "Microbiology", "Analytical Sciences" ], "hardSkills" : [ { "name" : "Microbiology", "level" : "intermediate" }, { "name" : "Analytical Sciences", "level" : "intermediate" } ], "majorSkills" : "Microbiology, Quality Control, Aseptic Processes", "majorSkillsList" : [ "Microbiology", "Quality Control", "Aseptic Processes" ], "coreResponsibilities" : "Perform microbiological testing, Issue analytical report, Adhere to SOPs, Document laboratory work, Assist Head of Microbiology lab, Complete GMP Self-Inspection, Present technical analytical data, Accomplish calibration of instruments, Maintain instruments, Report abnormal status, Report unexpected results, Maintain laboratory cleanliness, Maintain inventory of supplies, Support lean initiatives, Support Contamination Control Strategy, Support EMPQ execution, Support microbiology methods transfer, Support cleaning processes, Support disinfection efficacy, Support PQ of laboratory equipment, Ensure routine operation", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "cGMP requirements; Aseptic production; Microbiology; Biologics", "domainList" : [ "cgmp-requirements", "aseptic-production", "microbiology", "biologics" ], "domainSpecificKnowledge" : [ "cGMP requirements", "Aseptic production", "Microbiology", "Biologics" ], "communicationSkills" : "Fluent communications skills", "documentationSkills" : "Document laboratory work", "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "2 or more years of QC experience, Bachelor's Degree", "qualificationsPreferred" : "MNC Bio-pharma experience, QC new facility startup readiness, Project management skills, Life Sciences, Microbiology, or Analytical Sciences degree", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. ### ### The Position **Principle Roles & Responsibilities / Accountabilities****主要职责/责任** **Routine Operation:** * Perform the microbiological testing on the samples from incoming raw materials and packaging materials, produced bulks and products, environment monitoring, process validation and cleaning validation, etc. Issue the reliable analytical report in reasonable lead time. * Adhere to all effective SOPs and safety requirements and document laboratory work consistent with cGMP requirements * Assist Head of Microbiology lab to complete GMP Self-Inspection as well as the relevant CAPAs to maintain the global level of GMP compliance. * Presents technical analytical data clearly and concisely data to internal investigations and regulatory inspectors. * Accomplish the calibration and maintenance of assigned instruments, to ensure they are in good order to meet the analytical needs any time. * Report the abnormal status, unexpected results to supervisors with initiative. ● By reporting abnormal status and unexpected results during analysis processing by detailed data and information to alert supervisor to investigate and solve the problem in correct way and in time. * Maintain laboratory cleanliness and inventory of microbiology supplies * Supports lean initiatives in the area of lab operations, test method execution, documentation updates and equipment qualification **Engineering Project Support and Operation Readiness:** * CCS Support: Support the establishment of the Contamination Control Strategy (CCS) for the aseptic production line. * Environmental Monitoring (EM): Support EMPQ execution according to the project timeline. * Microbiology Method Validation: Support the microbiology methods transfer, including supporting the confirmation of cleaning and disinfection processes, and the efficacy of disinfectants. * Equipment Support: Support the Performance Qualification (PQ) of laboratory equipment and ensure routine operation. **Qualification and Experience****能力与经验** **Education/Qualifications** ● Bachelor’s Degree (Life Sciences, Microbiology, or Analytical Sciences is preferred) and above **Job Required Competencies** ● 2 or more years of QC experience, QC experience, with a focus on microbiology and aseptic processes. MNC Bio-pharma experience is preferred ● Sound knowledge of quality control procedures and legal standards, with experience in aseptic assurance and microbiological testing. ● Experienced in QC new facility startup readiness and operation ramp up is preferred. ● Fluent communications skills in English ● Project management skills are preferred. **** **** ### Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. **Roche is an Equal Opportunity Employer.**", "summaryDescription" : "Senior Analyst, Microbiology and Lab, Biologics at Roche. Skills: Microbiology, Quality Control, Aseptic Processes. Perform microbiological testing. Issue analytical report", "postedDate" : "2026-06-09T14:01:33.937", "createdAt" : "2026-06-11T14:01:33.602", "lastUpdated" : "2026-06-12T17:34:53.276", "ingestTimestamp" : "2026-06-11T14:01:33.602", "mongoId" : "6a26203374d8ee00a01fbee3", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://roche.wd3.myworkdayjobs.com/roche-ext/job/Shanghai/Senior-Analyst--Microbiology-and-EM-Lab--Biologics_202604-110281", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Microbiology", "Analytical Sciences", "Quality Control", "Aseptic Processes", "Microbiological testing", "Aseptic assurance", "Quality control procedures", "Laboratory operations", "Project management", "cGMP requirements", "Aseptic production", "Biologics" ], "skillCount" : 12, "jobCategory" : "engineering", "seniorityLevel" : "senior", "dataQualityScore" : 1.0, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "69cf26122beec4dd3d90b40b", "title" : "Laboratory Assistant- Microbiology", "company" : "Tampa General Hospital", "industry" : "Healthcare", "salary" : { "min" : 37000.0, "max" : 48000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level Laboratory Assistant in Tampa, Florida, adjusted for the healthcare industry and a large hospital setting." }, "location" : "United States-Florida-Tampa", "locations" : [ "United States-Florida-Tampa", "
TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

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Responsible for performing job duties in accordance with the mission, vision and values of Tampa General Hospital. High school diploma or GED. 1-2 months of on-the-job training and orientation. Previous work as a laboratory assistant is preferred. Tampa", "summaryDescription" : "Laboratory Assistant- Microbiology at Tampa General Hospital", "createdAt" : "2026-06-14T07:20:58.243", "lastUpdated" : "2026-06-15T13:45:56.776", "ingestTimestamp" : "2026-06-14T07:20:58.243", "mongoId" : "69cf26122beec4dd3d90b40b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 37000, "salaryAnnualMax" : 48000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.5555556, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.92 }, { "id" : "6a307525f292fd229c00c92f", "title" : "Senior Scientist, Biologics Drug Discovery", "company" : "Relation", "industry" : "Discovery", "salary" : { "min" : 75000.0, "max" : 110000.0, "currency" : "GBP", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior 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"Developability assessment", "Molecule optimisation", "Target validation", "Hit identification", "Lead characterization", "Candidate selection", "Biologics discovery", "Scientific decision-making", "Data interpretation", "Experimental execution", "Study design", "Data review", "Scientific interpretation", "Pipeline decisions" ], "hardSkillsList" : [ "Antibody discovery", "Antibody engineering", "Functional assays", "Biophysical characterization", "SPR", "BLI", "Octet" ], "softSkillsList" : [ "Mentoring" ], "hardSkills" : [ { "name" : "Antibody discovery", "level" : "intermediate" }, { "name" : "Antibody engineering", "level" : "intermediate" }, { "name" : "Functional assays", "level" : "intermediate" }, { "name" : "Biophysical characterization", "level" : "intermediate" }, { "name" : "SPR", "level" : "intermediate" }, { "name" : "BLI", "level" : "intermediate" }, { "name" : "Octet", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Mentoring" } ], "majorSkills" : "Biologics drug discovery, Antibody engineering, Machine learning", "majorSkillsList" : [ "Biologics drug discovery", "Antibody engineering", "Machine learning" ], "coreResponsibilities" : "Contribute to target assessment, Contribute to modality selection, Contribute to biologics discovery strategies, Design antibody molecules, Engineer antibody molecules, Optimise antibody molecules, Act as experienced scientist, Bring expertise in antibody discovery, Bring expertise in antibody engineering, Contribute to programme execution, Contribute to scientific decision-making, Translate biological insight, Design molecules, Engineer molecules, Optimise molecules, Design molecules with credible path, Engineer molecules with credible path, Optimise molecules with credible path, Act as technical voice, Partner with colleagues, Design molecules, Engineer molecules, Optimise molecules, Assess potency, Assess selectivity, Assess developability, Assess mechanism of action, Interpret complex datasets, Use data to drive molecule design, Use data to drive molecule optimisation, Maintain hands-on role, Partner with internal teams, Partner with external teams, Drive biologics programs end-to-end, Perform target validation, Perform hit identification, Perform lead characterization, Perform optimisation, Perform developability triage, Make modality decisions, Select molecule for target, Select molecule for indication, Design discovery packages, Oversee discovery packages, Combine cell-based assays, Combine biophysical characterization, Combine developability assessment, Drive candidate selection, Operate in matrixed environment, Partner with Computational Biology, Partner with Machine Learning, Partner with CMC, Partner with DMPK, Partner with Toxicology, Partner with Translational colleagues, De-risk candidates, Progress candidates toward IND-enabling studies, Partner with external collaborators, Partner with CROs, Contribute to study design, Contribute to data review, Contribute to scientific interpretation, Share expertise with colleagues, Contribute to scientific environment, Partner with ML teams, Partner with computational biology teams, Bring insight into predictive approaches, Bring insight into generative approaches, Apply predictive approaches to target selection, Apply generative approaches to target selection, Apply predictive approaches to molecule design, Apply generative approaches to molecule design, Apply predictive approaches to lead optimization, Apply generative approaches to lead optimization, Contribute to design of antibody molecules, Contribute to engineering of antibody molecules, Contribute to optimisation of antibody molecules, Use experimental data to guide decisions, Use experimental data to guide progression strategies, Contribute to scientific culture, Mentor junior scientists, Support publications, Support conference visibility, Shape scientific identity, Shape biologics group identity", "teamCollaboration" : "Interdisciplinary teams; Highly interdisciplinary teams; Matrixed pharmaiotech environment; Computational Biology; Machine Learning; CMC; DMPK; Toxicology; Translational colleagues; External collaborators; CROs; ML teams; Computational biology teams; Matrixed environment; Multiple stakeholders; Across teams; Across Drug Discovery; Across scientific domains; Across technical domains; Across operational domains; Multiple teams; Multiple projects; Shared company priorities; Diverse perspectives; Working relationships; Shared goals; Across teams", "domainKnowledge" : "Biologics drug discovery; Antibody discovery; Antibody engineering; Developability assessment; IND-enabling activities; Target Product Profiles; Antibodies; Bispecifics; ADCs; Fusion proteins; Fragments; Bone biology; Bone-microenvironment models; Osteoblast; Osteoclast; Mineral-binding assays; Resorption assays; TechBio; Computationally-driven discovery", "domainList" : [ "biologics-drug-discovery", "antibody-discovery", "antibody-engineering", "developability-assessment", "ind-enabling-activities", "target-product-profiles", "antibodies", "bispecifics", "adcs", "fusion-proteins", "fragments", "bone-biology", "bone-microenvironment-models", "osteoblast", "osteoclast", "mineral-binding-assays", "resorption-assays", "techbio", "computationally-driven-discovery" ], "domainSpecificKnowledge" : [ "Biologics drug discovery", "Antibody discovery", "Antibody engineering", "Developability assessment", "IND-enabling activities", "Target Product Profiles", "Antibodies", "Bispecifics", "ADCs", "Fusion proteins", "Fragments", "Bone biology", "Bone-microenvironment models", "Osteoblast", "Osteoclast", "Mineral-binding assays", "Resorption assays", "TechBio", "Computationally-driven discovery" ], "toolProficiency" : [ "SPRiacore", "BLI/Octet" ], "continuousLearning" : "Conference visibility", "problemSolvingSkills" : "Data-driven molecule optimisation", "qualificationsBasic" : "PhD in Molecular Biology, PhD in Immunology, PhD in Pharmacology, PhD in Cell Biology, PhD in Prot, Good understanding of biologics drug discovery end-to-end, Awareness of IND-enabling activities", "qualificationsPreferred" : "Familiarity with bone biology, Familiarity with bone-microenvironment models, Peer-reviewed publications, Prior experience mentoring junior scientists, Exposure to TechBio environment, Exposure to computationally-driven discovery environment", "remoteFriendly" : true, "workSiteFlexibility" : "Onsite", "rawDescription" : "ABOUT RELATION Relation is a sector defining TechBio company developing transformational medicines, with technology at our core. Our ambition is to understand human biology in unprecedented ways, discovering therapies to treat some of life’s most devastating diseases. We leverage single-cell multi-omics from patient tissue, functional assays, and machine learning to drive disease understanding, from cause to cure. We are scaling rapidly and building a team of exceptional individuals to push the boundaries of drug discovery. You will work in highly interdisciplinary teams where biology, computation, and engineering come together to solve complex problems that have not been solved before. Our state-of-the-art wet and dry labs in the heart of London are designed to accelerate this integration and translate insight into impact. We are committed to building diverse and inclusive teams. Relation is an equal opportunities employer and does not discriminate on the basis of gender, sexual orientation, marital or civil partnership status, gender reassignment, race, colour, nationality, ethnic or national origin, religion or belief, disability, or age. By joining Relation, you will help define how medicines are discovered and deliver meaningful impact for patients. THE OPPORTUNITY Relation is offering an outstanding opportunity for an Senior Scientist, Biologics Drug Discovery to bring deep biologics drug discovery knowledge to our growing pipeline. You will contribute to target assessment, modality selection and biologics discovery strategies through deep technical expertise and hands-on scientific execution from early concept through to IND-enabling studies. As Relation grows its scientific and machine learning capabilities, you will act as a highly experienced scientist, bringing deep expertise in antibody discovery and engineering while contributing directly to programme execution and scientific decision-making, working alongside our computational, ML, and translational teams to translate biological insight into well-designed molecules with a credible path to the clinic. We are particularly interested in scientists who have personally designed, engineered and optimised antibody molecules, including experience with affinity maturation, CDR engineering, developability assessment and data-driven molecule optimisation. You will additionally be a key technical voice in pipeline decisions and a trusted partner to colleagues across Drug Discovery and beyond. DAY TO DAY, YOU WILL - Demonstrated hands-on experience designing, engineering and optimising antibody molecules, with a strong understanding of the experimental approaches used to assess potency, selectivity, developability and mechanism of action. - Ability to independently interpret complex datasets and use those data to drive molecule design and optimisation decisions. - Maintain a hands-on role in biologics discovery activities while partnering closely with internal and external teams. - Drive biologics programs end-to-end — from target validation and hit identification through lead characterization, optimization, and developability triage — against agreed Target Product Profiles (TPPs). - Make informed modality decisions across the biologics landscape (antibodies, bispecifics, ADCs, fusion proteins, fragments) and ensure the right molecule is selected for the right target and indication. - Design and oversee fit-for-purpose discovery packages, combining cell-based functional assays, biophysical characterization (SPR/Biacore, BLI/Octet), and developability assessment to drive sound candidate selection. - Operate effectively in a matrixed pharma/biotech environment, partnering with Computational Biology, Machine Learning, CMC, DMPK, Toxicology, and Translational colleagues to de-risk candidates and progress them toward IND-enabling studies. - Partner with external collaborators and CROs, contributing to study design, data review and scientific interpretation. - Share expertise with colleagues and contribute to a collaborative scientific environment. - Partner with our ML and computational biology teams to bring biologics drug discovery insight into how predictive and generative approaches are applied to target selection, molecule design, and lead optimization. - Personally contribute to the design, engineering and optimisation of antibody molecules, using experimental data to guide scientific decisions and progression strategies. - Contribute to Relation’s scientific culture by mentoring junior scientists in biologics drug discovery, supporting publications and conference visibility, and helping to shape the broader scientific identity of the biologics group. PROFESSIONALLY, YOU WILL HAVE - A PhD. in Molecular Biology, Immunology, Pharmacology, Cell Biology, Protein Engineering, or a related life-science discipline. - Hands-on drug discovery experience gained in a pharma or biotech setting, with a clear track record of contributing to biologics programs progressing through key discovery milestones (target validation, hit-to-lead, lead optimization, candidate selection). - Proven experience working in a matrixed pharma/biotech environment, partnering effectively across functions (e.g. CMC, DMPK, Toxicology, Computational/ML, Translational) and balancing multiple stakeholders. - Deep working knowledge of biologics drug discovery: how biology is translated into a molecule, how modalities are chosen, how discovery cascades are designed, and what data are needed at each stage to make sound progression decisions. - Familiarity with the biologics modality landscape (antibodies, bispecifics, ADCs, fusion proteins, fragments) and an informed view of when each modality is the right tool for the biology. - Hands-on experience with the data types that drive biologics drug discovery decisions, including cell-based functional and screening assays and biophysical characterization (SPR/Biacore, BLI/Octet). - Working experience of CRO management across biologics drug discovery activities (e.g. molecule production, in vitro pharmacology, in vivo studies). - A good understanding of biologics drug discovery end-to-end, including TPP-driven decision-making, developability considerations, and awareness of what is required to support IND-enabling activities. - Curiosity about how ML and computational approaches can complement traditional biologics discovery workflows, and an interest in shaping how those tools are deployed. Bonus experience: - Familiarity with bone biology and bone-microenvironment models (osteoblast, osteoclast, osteocyte; mineral-binding or resorption assays). - Peer-reviewed publications in the biologics drug discovery space, prior experience mentoring junior scientists, and exposure to a TechBio or computationally-driven discovery environment are also welcome. PERSONALLY, YOU: - Are comfortable working in a matrixed environment, balancing multiple stakeholders and contributing effectively across teams. - Take ownership of your work, proactively seek opportunities to contribute, and enable others to do their best work. - Communicate openly and directly, give and receive feedback constructively, and handle challenging conversations with respect. - Actively seek out diverse perspectives, build strong working relationships, and contribute to shared goals across teams. - Embrace challenges with openness and resilience, set high standards for yourself, and strive to deliver meaningful outcomes. WORKING STYLE & CULTURE AT RELATION At Relation, we operate in a matrixed, interdisciplinary environment, where impact is driven through collaboration across scientific, technical, and operational domains. We collaborate, and you will partner with colleagues across multiple teams and projects, contributing your expertise while aligning to shared company priorities. We work together and win together! The patient is waiting! RECRUITMENT AGENCIES Please note that Relation does not accept unsolicited resumes from agencies. Resumes should not be forwarded to our job aliases or employees. Relation will not be liable for any fees associated with unsolicited CVs. Relation is a committed equal opportunities employer.", "summaryDescription" : "Senior Scientist, Biologics Drug Discovery at Relation. Skills: Biologics drug discovery, Antibody engineering, Machine learning. Contribute to target assessment. Contribute to modality selection", "createdAt" : "2026-06-16T00:28:21.999", "lastUpdated" : "2026-06-16T08:47:15.704", "ingestTimestamp" : "2026-06-16T00:28:21.999", "mongoId" : "6a307525f292fd229c00c92f", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Antibody discovery", "Antibody engineering", "Functional assays", "Biophysical characterization", "SPR", "BLI", "Octet", "Mentoring", "Biologics drug discovery", "Machine learning", "Drug discovery", "Molecule design", "Affinity maturation", "CDR engineering", "Developability assessment", "Molecule optimisation", "Target validation", "Hit identification", "Lead characterization", "Candidate selection", "Biologics discovery", "Scientific decision-making", "Data interpretation", "Experimental execution", "Study design", "Data review", "Scientific interpretation", "Pipeline decisions", "IND-enabling activities", "Target Product Profiles", "Antibodies", "Bispecifics", "ADCs", "Fusion proteins", "Fragments", "Bone biology", "Bone-microenvironment models", "Osteoblast", "Osteoclast", "Mineral-binding assays", "Resorption assays", "TechBio", "Computationally-driven discovery", "SPRiacore", "BLI/Octet" ], "skillCount" : 45, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 0.8888889, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2a67f274d8ee00a06320f5", "title" : "Chemical Engineer, PCB (Starlink)", "company" : "SpaceX", "industry" : "Technology", "salary" : { "min" : 95000.0, "max" : 135000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Junior Chemical Engineer in the Technology industry in Bastrop, United States, adjusted for SpaceX's company size and industry." }, "location" : "Bastrop, TX, United States", "locations" : [ "Bastrop", "TX", "United States" ], "timestamp" : "2026-06-13T10:14:37.766", "fingerprint" : "25727383daab49751820d7e95fd3faec26fd1c9c9c0191c08833b0f33adb290b", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://boards.greenhouse.io/spacex/jobs/8562076002?gh_jid=8562076002", "externalId" : "8562076002", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Bastrop", "state" : "Texas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "30.0541116,-97.3887764" } ], "locationText" : "Bastrop, Texas, United States", "technicalSkills" : "PCB fabrication, Metal plating, Copper etching, Electroless metallization, Water treatment, Chemical waste treatment, Plasma etching", "professionalSkills" : [ "Process development", "Mass production", "Machine design", "Process DOE", "Defect characterization", "Root cause analysis", "Project planning", "Cost-benefit analysis", "Machine activation" ], "hardSkillsList" : [ "Physics-based analysis", "Statistical methodologies", "DOE" ], "softSkillsList" : [ "Organizational skills", "Written communication skills", "Oral communication skills" ], "hardSkills" : [ { "name" : "Physics-based analysis", "level" : "intermediate" }, { "name" : "Statistical methodologies", "level" : "intermediate" }, { "name" : "DOE", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Organizational skills" }, { "name" : "Written communication skills" }, { "name" : "Oral communication skills" } ], "majorSkills" : "PCB manufacturing, Process engineering, Chemical recycling", "majorSkillsList" : [ "PCB manufacturing", "Process engineering", "Chemical recycling" ], "coreResponsibilities" : "Develop manufacturing processes, Implement manufacturing processes, Maintain manufacturing processes, Develop chemical recycling strategies, Develop mass production processes, Become PCB fabrication expert, Own PCB production processes, Perform machine design, Run process DOEs, Interact with senior leadership, Analyze production processes, Analyze machinery, Develop experiments, Diagnose manufacturing problems, Correct manufacturing problems, Perform defect characterization, Perform defect analysis, Develop action plans, Develop project plans, Develop budgets, Develop cost-benefit analysis, Own machine activation, Perform machine testing", "teamCollaboration" : "Cross-functional team; Small team of engineers; Team of technicians", "projectManagementSkills" : [ "Project planning", "Budgeting", "Cost-benefit analysis" ], "domainKnowledge" : "PCB manufacturing; Chemical engineering; Environmental strategies; Satellite constellations; High-speed internet", "domainList" : [ "pcb-manufacturing", "chemical-engineering", "environmental-strategies", "satellite-constellations", "high-speed-internet" ], "domainSpecificKnowledge" : [ "PCB manufacturing", "Chemical engineering", "Environmental strategies", "Satellite constellations", "High-speed internet" ], "communicationSkills" : "Written communication; Oral communication", "problemSolvingSkills" : "Root cause analysis; Troubleshooting", "specialRequirements" : "Ability to travel frequently, Lift 25 lbs. unassisted, Lifting, Standing, Climbing, Bending, Grasping, Sitting, Pulling, Pushing, Stooping, Stretching, Carrying, ITAR requirements", "qualificationsBasic" : "Bachelor's degree in engineering, 1+ years chemical engineering experience", "qualificationsPreferred" : "Master's degree in chemistry, Master's degree in chemical engineering, Master's degree in materials science, Master's degree in environmental, Hands-on experience with complex fluid systems, Hands-on experience with mechanical production systems, Experience transitioning products to manufacturing, Experience scaling to high volume, Experience with PCB manufacturing processes", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this possible, with the ultimate goal of enabling human life on Mars. CHEMICAL ENGINEER, PCB (STARLINK) Starlink believes in providing fast, reliable internet to those that need it most. We design, build, and launch the world's largest and most advanced satellite constellation that is capable of delivering high-speed internet to even the most remote locations. And while our hardware and network are incredibly advanced, we keep the end-user experience impressively simple - our customers have internet within 10 minutes of unboxing. As a Chemical Engineer on Starlink, you will spearhead state of the art production processes for our printed circuit boards (PCBs). You will design and implement environmentally friendly chemical recycling strategies, develop highly capable processes for use in mass production, and become a multi-disciplinary expert in PCB fabrication. Your work will form the backbone for millions of next generation consumer facing devices that we ship directly to customers and businesses all over the world. From private homes, RVs, planes, or boats, this team plays an instrumental role in leveling the playing field for high-speed connectivity. You will own various PCB production processes, from initial machine design to running hands-on process DOEs, and will interact regularly with senior leadership during critical design phases. By the end of this year, the Starlink factory in Bastrop will be the largest PCB manufacturing facility, by volume, in North America. RESPONSIBILITIES: Responsible for developing, implementing, and maintaining new and/or improved manufacturing processes, equipment, technologies, and facilities. Examples could include metal plating lines, copper etching lines, direct or electroless metallization lines, water and chemical waste treatment, plasma etching systems, etc. Analyze production processes and machinery from a first principles, physics-based approach Develop experiments to diagnose and correct manufacturing problems, utilizing robust DOE and statistical methodologies Perform defect characterization and analysis to determine root cause and develop action plans to improve yields Develop project plans, budgets, and cost/benefit analysis for implementation of new processes or machines Own and perform machine activation and testing with a small team of engineers and technicians BASIC QUALIFICATIONS: Bachelor’s degree in an engineering discipline 1+ years of experience in chemical engineering design, analysis, and/or system implementation (internship and extracurricular experience is applicable) PREFERRED SKILLS AND EXPERIENCE: Master’s degree in chemistry, chemical engineering, materials science, environmental, or related technical discipline Hands-on experience working with complex fluid or mechanical based production systems in a professional setting Experience transitioning products from design to manufacturing and scaling to high volume as part of a cross-functional team Self-motivated with strong organizational, written, and oral communication skills Experience with PCB manufacturing processes like metal plating lines, copper etching lines, direct or electroless metallization lines, water and chemical waste treatment, plasma etching systems, etc. ADDITIONAL REQUIREMENTS: Ability to travel frequently for work, potentially for extended periods of time during machine buyoffs and startup Ability to lift 25 lbs. unassisted Lifting, standing, climbing, bending, grasping, sitting, pulling, pushing, stooping, stretching, and carrying are generally required to perform the functions of this position ITAR REQUIREMENTS: To conform to U. S. Government export regulations, applicant must be a (i) U. S. citizen or national, (ii) U. S. lawful, permanent resident (aka green card holder), (iii) Refugee under 8 U.S. C. § 1157, or (iv) Asylee under 8 U.S. C. § 1158, or be eligible to obtain the required authorizations from the U. S. Department of State. Learn more about the ITAR here. SpaceX is an Equal Opportunity Employer; employment with SpaceX is governed on the basis of merit, competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability or any other legally protected status. Applicants wishing to view a copy of SpaceX’s Affirmative Action Plan for veterans and individuals with disabilities, or applicants requiring reasonable accommodation to the application/interview process should reach out to EEOCompliance@spacex.com.", "summaryDescription" : "Chemical Engineer, PCB (Starlink) at SpaceX. Skills: PCB manufacturing, Process engineering, Chemical recycling. Develop manufacturing processes. Implement manufacturing processes", "postedDate" : "2026-06-11T18:26:27.747", "createdAt" : "2026-06-11T18:26:27.747", "lastUpdated" : "2026-06-13T10:14:37.766", "ingestTimestamp" : "2026-06-11T18:26:27.747", "mongoId" : "6a2a67f274d8ee00a06320f5", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 95000, "salaryAnnualMax" : 135000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Physics-based analysis", "Statistical methodologies", "DOE", "Organizational skills", "Written communication skills", "Oral communication skills", "PCB manufacturing", "Process engineering", "Chemical recycling", "Process development", "Mass production", "Machine design", "Process DOE", "Defect characterization", "Root cause analysis", "Project planning", "Cost-benefit analysis", "Machine activation", "Budgeting", "Chemical engineering", "Environmental strategies", "Satellite constellations", "High-speed internet" ], "skillCount" : 23, "jobCategory" : "engineering", "jobSubcategory" : "starlink-production-bastrop---pcb-engineering", "dataQualityScore" : 0.7777778, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology" }, { "id" : "6a2cc22774d8ee00a0a058b8", "title" : "Director of Performance / Head of Performance", "company" : "Rumble Boxing", "industry" : "Sports & Fitness", "salary" : { "min" : 145000.0, "max" : 210000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Director of Performance in Vancouver, Canada, adjusted for the sports & fitness industry and company size." }, "location" : "Vancouver, BC", "locations" : [ "Vancouver", "BC" ], "timestamp" : "2026-06-16T01:36:41.846", "fingerprint" : "fc34cfdb119655d834ff3ff72b4dd8e6f5a649c9bca32992d11859b6f5048e7e", "source" : "breezyhr", "language" : "en", "applyUrl" : "https://rumble-boxing.breezy.hr/p/37b69e1de02b-director-of-performance-head-of-performance", "externalId" : "37b69e1de02b", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Vancouver", "state" : "British Columbia", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "49.2608724,-123.1139520" } ], "locationText" : "Vancouver, British Columbia, Canada", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "coreResponsibilities" : "Build performance and wellness ecosystem, Combine boxing, Combine strength & conditioning, Combine recovery, Combine mobility, Combine longevity, Combine performance lifestyle", "domainKnowledge" : "Performance lifestyle", "domainList" : [ "performance-lifestyle" ], "domainSpecificKnowledge" : [ "Performance lifestyle" ], "rawDescription" : "Director of Performance / Head of Performance Rumble Wellness GroupABOUT THE ROLERumble is evolving beyond boutique fitness.We are building a modern performance and wellness ecosystem combining:* boxing* strength & conditioning* recovery* mobility* longevity* performance lifestyleWe are looking", "summaryDescription" : "Director of Performance / Head of Performance at Rumble Boxing. Build performance and wellness ecosystem. Combine boxing", "createdAt" : "2026-06-14T19:37:09.041", "lastUpdated" : "2026-06-16T01:36:41.846", "ingestTimestamp" : "2026-06-14T19:37:09.041", "mongoId" : "6a2cc22774d8ee00a0a058b8", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Performance lifestyle" ], "skillCount" : 1, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Sports & Fitness", "llmIndustryConfidence" : 0.92 }, { "id" : "6a2a475974d8ee00a05d9775", "title" : "Supervisor, Chemical Engineering", "company" : "Allison", "salary" : { "min" : 105000.0, "max" : 145000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Lead, Mid-level Chemical Engineering Supervisor in Manufacturing in Indianapolis, United States, adjusted for company size and industry." }, "location" : "Indianapolis, IN", "locations" : [ "Indianapolis, IN", "United States of America" ], "timestamp" : "2026-06-13T08:52:26.845", "fingerprint" : "177a52dd5f00b680583aec735efcc051038146d742b9125d31407f1675fe175e", "source" : "workday", "language" : "en", "applyUrl" : "https://allisontransmission.wd1.myworkdayjobs.com/ATI-External/job/Indianapolis-IN/Supervisor--Chemical-Engineering_R007737", "externalId" : "R007737", "locationPoint" : "39.76838,-86.15804", "structuredLocations" : [ { "city" : "Indianapolis", "state" : "Indiana", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "39.7683331,-86.1583502" } ], "locationText" : "Indianapolis, Indiana, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 1, "experienceMaxYears" : 5, "experienceLevel" : "Mid", "professionalSkills" : [ "Chemical processing", "Environmental compliance", "Safety compliance" ], "hardSkillsList" : [ "Chemical processing", "Environmental compliance", "Safety compliance", "Record keeping" ], "softSkillsList" : [ "Adaptability" ], "hardSkills" : [ { "name" : "Chemical processing", "level" : "intermediate" }, { "name" : "Environmental compliance", "level" : "intermediate" }, { "name" : "Safety compliance", "level" : "intermediate" }, { "name" : "Record keeping", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Adaptability" } ], "majorSkills" : "Chemical processing, Supervision, Safety compliance", "majorSkillsList" : [ "Chemical processing", "Supervision", "Safety compliance" ], "coreResponsibilities" : "Manage daily activities of Oil Stores personnel, Maintain UAWCAS reporting, Maintain hourly timekeeping in Workday, Approve vacations, Communicate with Engineering Team peers, Work and communicate to hourly personnel, Assure compliance to restrictions and requirements, Train and develop employees, Plan and schedule meetings, Schedule programs, Schedule projects, Complete work assignments within constraints, Produce quality reports, Produce financial reports, Produce environmental reports, Produce performance reports, Implement safety policies, Support corporate safety policies, Implement good housekeeping standards, Record and organize information, Communicate with management, Communicate with internal customers, Relay information regarding constraints, Relay information regarding schedules, Relay information regarding closures, Relay information regarding production impacts, Problem solve, Provide viable solutions", "teamCollaboration" : "Engineering Team peers; Hourly personnel; Management; Internal customers", "domainKnowledge" : "Basic chemistry; Industrial chemicals; Metallurgy", "domainList" : [ "basic-chemistry", "industrial-chemicals", "metallurgy" ], "domainSpecificKnowledge" : [ "Basic chemistry", "Industrial chemicals", "Metallurgy" ], "toolProficiency" : [ "Workday", "Excel", "Power Point" ], "communicationSkills" : "Reports; Presentations; Emails; Verbal communication", "continuousLearning" : "Tuition assistance program", "innovationCreativity" : "Innovation", "problemSolvingSkills" : "Problem solve; Provide viable solutions", "specialRequirements" : "Handling small amounts of chemicals, Compliance with Safety PPE, Safety-Toe shoes, Eye protection, Hearing protection, Chemical gloves, Physical presence in workplace", "outcomesObjectives" : "Improve the Way the World Works", "qualificationsBasic" : "Associate degree or equivalent experience, 1+ years supervisory experience, Understanding of basic chemistry", "qualificationsPreferred" : "1+ years working in industrial manufacturing, Knowledge of industrial chemicals and their interaction with metallurgy, Experience working with Excel and Power Point", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**JOIN THE TEAM THAT’S POWERING PROGRESS** Building cities. Driving commerce. Fueling Progress. For over 100 years, Allison has powered the vehicles and technology that move our world forward. What powers us? Our employees. From the first person hired by James Allison in 1915 to the thousands across the globe who work for Allison today, we're driving progress everywhere because we employ top talent worldwide. In both the Allison Transmission and Allison Off-Highway Drive and Motion Systems business units, our team strives to Improve the Way the World Works. Learn more about this role and how you can begin _driving your career forward!_ **Benefits:** The below list features some of the benefits currently available. Eligibility may be subject to the terms and conditions of governing documents and available benefits may be subject to change at the company’s discretion. * Choice of medical plans with prescription coverage * Employer HSA contribution * Dental & Vision Insurance * Paid Parental Leave * Short & Long-Term Disability * Other voluntary benefits including: Critical Illness, Hospital Indemnity, Identity Theft Protection and Pet Insurance * 401K with generous Company match & contribution * Accrued Paid Time Off * 12 Paid Holidays + 1 Floating Holiday * Robust employee wellness program * Tuition assistance program **Job Description:** **Key Responsibilities: ** * Responsible for managing daily activities of Oil Stores personnel. * Responsible for maintaining UAWCAS reporting, Hourly timekeeping in Workday, and approval of Vacations. * Communicate with Engineering Team peers in various cross functional projects. * Work and communicate to hourly personnel and assure compliance to federal, state, local and Allison restrictions and requirements. * Train and develop employees in areas concerning chemical processing, environmental and safety. * Plan and schedule chemical, safety and processing related meetings, programs, and projects in accordance with Allison policies and procedures. * Complete work assignments within budget, manpower and timing constraints. * Produce quality, financial, environmental and performance reports per the Allison system. * Implements and actively supports the plant and corporate safety policies and initiatives. * Physical presence in the workplace is an essential function. * Implements safety and good housekeeping standards. * Able to record and organize information in a readily retrievable format. * Capable of working and communicating with management and internal customers to relay information in form of reports, presentation, emails or verbally in regard to constraints, schedules, closures, or anything that may affect production. * Problem solve and provide viable solutions to meet internal customer demands. **Key Performance Measures: ** Safety Productivity Quality Responsiveness Cost **Competencies and Behaviors: ** * **Adhering to the highest standards in what we do**. We succeed through integrity, trust, and quality as we drive for results. * **Drive a positive customer experience**. We deliver better outcomes when we understand our customers’ needs and execute appropriately. * **Improve the way the world works**. We develop better solutions through innovation and a continuous desire to improve. * **Leveraging the power of teamwork**. We develop better solutions by working together toward a common goal. **Qualifications: ** Required: Associate degree and\\or equivalent experience in manufacturing, supervision or industrial chemicals **Experience: ** Required: 1+ years supervisory experience Understanding of basic chemistry Preferred: 1+ years working in industrial manufacturing Knowledge of industrial chemicals and their interaction with metallurgy Experience working with Excel and Power Point **Scope Factors ** Confident and capable of handling small amounts of chemicals Compliance in adhering to all of Allison’s Safety PPE. Safety-Toe shoes, Eye protection, hearing protection, chemical gloves. Adapting to various personalities, attitudes, and cultures. Allison Transmission is an equal opportunity employer. We have opportunities for all qualified applicants regardless of age, race, color, sex, religion, creed, national origin, disability, sexual orientation, gender identity/expression or veteran status. If you are an individual with a disability or a disabled veteran requiring assistance and/or reasonable accommodations reviewing any of the careers information, please contact us at _[ati +ask4max@service-now.com](mailto:ati+ask4max@service-now.com)_. Please note that Allison Transmission will make an offer of employment only to individuals who have applied for a position using our official application. Be on alert for possible fraudulent offers of employment. Allison Transmission will not solicit money or banking information from applicants.", "summaryDescription" : "Supervisor, Chemical Engineering at Allison. Skills: Chemical processing, Supervision, Safety compliance. Manage daily activities of Oil Stores personnel. Maintain UAWCAS reporting", "postedDate" : "2026-06-10T15:38:07.571", "createdAt" : "2026-06-11T15:38:07.485", "lastUpdated" : "2026-06-13T08:52:26.845", "ingestTimestamp" : "2026-06-11T15:38:07.485", "mongoId" : "6a2a475974d8ee00a05d9775", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://allisontransmission.wd1.myworkdayjobs.com/ATI-External/job/Indianapolis-IN/Supervisor--Chemical-Engineering_R007737", "salaryAnnualMin" : 105000, "salaryAnnualMax" : 145000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Chemical processing", "Environmental compliance", "Safety compliance", "Record keeping", "Adaptability", "Supervision", "Basic chemistry", "Industrial chemicals", "Metallurgy", "Workday", "Excel", "Power Point" ], "skillCount" : 12, "jobCategory" : "engineering", "seniorityLevel" : "mid", "dataQualityScore" : 1.0, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2c7d6174d8ee00a094fa98", "title" : "Group Food Safety & Microbiology Manager", "company" : "THG", "industry" : "Food & Beverage", "salary" : { "min" : 65000.0, "max" : 95000.0, "currency" : "GBP", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Manager in the Food & Beverage industry in Manchester, United Kingdom, adjusted for seniority and company size." }, "location" : "Manchester, England, United Kingdom", "locations" : [ "Manchester", "England", "United Kingdom" ], "timestamp" : "2026-06-16T00:59:22.672", "fingerprint" : "f11c669fcd9b32a3922814cf8b1d67ceec9a28523743de4dce5ebff9291629aa", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://www.thg.com/talent/job-search?gh_jid=4876369101", "externalId" : "4876369101", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Manchester", "state" : "England", "country" : "United Kingdom", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "53.4424618,-2.2324547" } ], "locationText" : "Manchester, England, United Kingdom", "employmentType" : "FULL_TIME", "experienceLevel" : "Manager", "technicalSkills" : "Food microbiology", "professionalSkills" : [ "Risk assessment", "Technical authority", "Microbiological governance", "Due diligence", "Data interpretation" ], "hardSkillsList" : [ "Microbiological testing", "Shelf-life determination", "HACCP reviews", "Environmental monitoring programmes", "Root cause analysis", "Corrective action plans", "Supplier capability assessment" ], "hardSkills" : [ { "name" : "Microbiological testing", "level" : "intermediate" }, { "name" : "Shelf-life determination", "level" : "intermediate" }, { "name" : "HACCP reviews", "level" : "intermediate" }, { "name" : "Environmental monitoring programmes", "level" : "intermediate" }, { "name" : "Root cause analysis", "level" : "intermediate" }, { "name" : "Corrective action plans", "level" : "intermediate" }, { "name" : "Supplier capability assessment", "level" : "intermediate" } ], "majorSkills" : "Food safety, Microbiology, Risk management", "majorSkillsList" : [ "Food safety", "Microbiology", "Risk management" ], "coreResponsibilities" : "Define group microbiological strategy, Manage contract laboratory relationships, Act as escalation point for risk, Establish risk-based criteria, Provide expert input into shelf-life, Develop harmonised microbiological standards, Ensure alignment with standards, Lead microbiological input into HACCP, Define environmental monitoring programmes, Lead microbiological risk assessments, Take ownership of high-risk incidents, Direct root cause analysis, Provide technical justification for disposition, Provide technical oversight, Assess supplier microbiological capability, Support due diligence activities, Drive consistency across manufacturing, Interpret microbiological data, Develop predictive monitoring approach, Define KPIs for performance, Influence adoption of digital systems", "teamCollaboration" : "Site leadership; Suppliers; Customers; Operations teams; Technical teams; NPD teams; Commercial teams; Central teams; Site technical teams; Third-party manufacturers", "domainKnowledge" : "Food microbiology; Manufacturing environments; BRCGS standards; Retailer standards; International regulatory requirements", "domainList" : [ "food-microbiology", "manufacturing-environments", "brcgs-standards", "retailer-standards", "international-regulatory-requirements" ], "domainSpecificKnowledge" : [ "Food microbiology", "Manufacturing environments", "BRCGS standards", "Retailer standards", "International regulatory requirements" ], "communicationSkills" : "Translate complex risk", "continuousLearning" : "Bespoke development programmes; Up-skilling programme", "problemSolvingSkills" : "Risk-based decision making", "qualificationsBasic" : "5+ years food safety experience, 5+ years microbiology experience, Experience in complex manufacturing environments, Risk-based decision making experience", "qualificationsPreferred" : "Experience with BRCGS standards, Experience with retailer standards, Experience with international regulatory requirements", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "About THG We are THG, a global ecommerce group on a mission to be the global online leader in beauty and sports nutrition. Our portfolio of leading retailers and brands such as LOOKFANTASTIC, Myprotein, ESPA, Perricone MD, and Cult Beauty form our two core businesses: THG Beauty and THG Nutrition. From Manchester to New York, we’re powered by a team of over 2500 people who work together, lead by example, and think BIG. With us, you’ll go further, faster. What are you waiting for? Job Title: Group Food Safety & Microbiology Manager Reporting to: Head of Technical Location: THG HQ, Icon 1, WA15 0AF About THG Nutrition THG Nutrition is home to some of the best-loved and most trusted names in wellbeing and nutrition, including Myprotein, the world's largest online sports nutrition brand, its family of brands, Myvegan, Myvitamins & MP Activewear. We want to be the world's most empowering health movement, championing everyone to live healthier, more active lives. Our brands and people exist to break boundaries, to power and to empower those who want more. Everything we do is in-house, from manufacturing and new product development to content creation, e-commerce, marketing and logistics. This means we’re perfectly positioned to deliver to our vision and keep our place at the top of a fast-moving, global industry. It's an incredibly exciting time to join the team, and we’re always looking for talented people who share our vision and values to drive our Nutrition movement forward. About the Role We are seeking a highly experienced Food Safety Microbiology Lead to act as the central technical authority for microbiological and food safety risk across THG Nutrition’s processes and global manufacturing network. This is a senior, non-laboratory role responsible for defining microbiological strategy, setting group-wide standards, and providing expert judgement on food safety risk. You will operate at a strategic and operational level, influencing site leadership, suppliers, and customers, and taking ownership of microbiological governance across multiple sites and product categories. The role requires a deep understanding of food microbiology in complex manufacturing environments, combined with the ability to make risk-based decisions at pace. Key Responsibilities Group Microbiological Strategy & Technical Authority Own and define the group microbiological strategy across all manufacturing sites and product categories Manage the requirements and relationship between THG Nutrition and contract laboratories used for testing Act as the final escalation point and decision-maker for microbiological risk, deviations, and food safety incidents Establish and maintain risk-based microbiological criteria, specifications, and testing strategies aligned to product and process risk Provide expert input into shelf-life determination, challenge testing, and validation of control measures Governance, Standards & Compliance Develop and implement harmonised microbiological standards across supplier base, internal sites and third-party manufacturers Ensure alignment with BRCGS, retailer standards, and international regulatory requirements Lead microbiological input into HACCP reviews, ensuring hazards are correctly identified, assessed, and controlled Define and standardise environmental monitoring programmes (EMP) across the manufacturing network Risk Management & Incident Leadership Lead microbiological risk assessments across raw materials, processes, and finished products Take ownership of high-risk incidents, including pathogen detections, trend failures, and product safety concerns Direct root cause analysis and corrective action plans for microbiological non-conformances Provide clear, defensible technical justification for product disposition decisions Multi-Site & Supplier Oversight Provide technical oversight and challenge to central teams, site technical teams and third-party manufacturers Assess microbiological capability and controls within the supply base, influencing approval and ongoing compliance Support due diligence activities, audits, and site reviews from a microbiological and food safety perspective Drive consistency and best practice across a diverse, multi-site manufacturing network Data, Trending & Predictive Insight Own the interpretation of microbiological data across the group, identifying emerging risks and systemic issues Develop a more predictive, risk-based approach to microbiological monitoring and control Define KPIs and reporting frameworks for microbiological performance at group level Influence the adoption of digital systems and tools to enhance data visibility and decision making Cross-Functional Influence Partner with Operations, Technical, NPD, and Commercial teams to embed microbiological risk management across the product lifecycle Provide technical input into process design, factory layouts, and capital investment decisions Act as the microbiology lead in customer and regulatory interactions where required Skills & Experience Required Degree (or higher) in Microbiology, Food Microbiology, or a closely related discipline Extensive experience in food manufacturing, with deep expertise in microbiological risk within complex, multi-product environments Proven track record of operating at a senior technical level, influencing multiple sites or business units Advanced knowledge of: Pathogens of concern (e. g. Salmonella, Listeria, E. coli) and control strategies Environmental monitoring and hygienic zoning principles Shelf-life validation, challenge testing, and predictive microbiology HACCP methodology and risk assessment frameworks Strong working knowledge of BRCGS and global food safety standards Personal Attributes Credible technical authority, able to challenge and influence senior stakeholders Decisive, with the ability to make risk-based calls under pressure Highly analytical, with strong attention to detail and systems thinking Pragmatic and commercially aware, balancing risk with business needs Strong communicator, able to translate complex microbiological risk into clear actions What’s in it for me? Career Development Access bespoke development programmes that have been designed and developed by our in-house L&D team. Continued development through our up-skilling programme that is delivered in partnership with an industry-leading training provider. Enhanced Leave 25 days annual leave plus bank holidays. Don’t want to work on your birthday? We don’t either! Enjoy your day off on us! Enhanced maternity and paternity pay, depending on length of service. Up to 10 days compassionate leave. Buy back up to 3 days each year. Unlock 2 days volunteer leave after 12-months. Wellbeing Support Access face-to-face and virtual appointments with our in-house GP. Access our 247 Employee Assistance Programme (EAP) which is provided by Bupa. State-of-the-art on-site gym. Access to our on-site physio. Other Perks Save up to 12% on the cost of personal tech through our salary sacrifice scheme. Subsidised bus pass from Manchester City Centre to our ICON office. Up to 50% staff discount on THG brands. On-site staff shop. Know someone who would be perfect for THG? Refer them and get up to £1000 when they pass their probation. Anniversary gifts when you hit 5 and 10 years of service THG is proud to be a Disability Confident Committed employer. If you are invited to interview, please let us know if there are any reasonable adjustments we can make to the recruitment process that will enable you to perform to the best of your ability. THG is committed to creating a diverse & inclusive environment and hence welcomes applications from all sections of the community. Because of the high volumes of applications our opportunities attract, it sometimes takes us time to review and consider them all. We endeavour to respond to every application we receive within 14 days. If you haven't heard from us within that time frame or should you have any specific questions about this or other applications for positions at THG please contact one of our Talent team to discuss further.", "summaryDescription" : "Group Food Safety & Microbiology Manager at THG. Skills: Food safety, Microbiology, Risk management. Define group microbiological strategy. 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Our partner is looking for a Biological Safety Specialist based in Spain. This role sits at the intersection of science, regulation, and medical device innovation, ensuring that products meet the highest standards of biological safety throughout their development lifecycle. You will contribute directly to the safety and compliance of medical technologies that impact patient health globally. Working within a highly specialized and regulated environment, you will evaluate scientific data, assess biocompatibility, and support the creation of critical regulatory documentation. The position involves close collaboration with multidisciplinary teams and external stakeholders to ensure alignment with international standards. You will play a key role in shaping safety assessments that influence product approval and market readiness. This is a detail-driven and impact-focused role suited for professionals passionate about science, compliance, and healthcare innovation. ## Accountabilities Develop, review, and maintain biological safety documentation and reports in compliance with applicable international standards and medical device regulations. Assess and audit biocompatibility and material characterization data to ensure alignment with regulatory requirements and safety expectations. Interpret complex scientific and technical information to support risk assessments and regulatory submissions for medical devices. Collaborate with cross-functional teams to ensure biological safety considerations are integrated throughout the product development lifecycle. Review and contribute to the development of complex technical and regulatory documents with a high level of accuracy and scientific rigor. Support continuous improvement of biological safety processes, methodologies, and compliance frameworks. Requirements: Bachelor’s degree with at least 5 years of relevant experience, or Master’s/Doctorate degree with at least 2 years of relevant experience in a scientific or related discipline. Strong knowledge of medical device regulations and international standards related to biological safety and biocompatibility. Experience assessing compliance of biocompatibility studies and material characterization against regulatory requirements. Proven ability to write, review, and manage complex technical and regulatory documentation. Strong analytical and critical thinking skills with attention to detail and scientific accuracy. Proficiency in Microsoft Word and other standard documentation tools. Fluency in English; proficiency in the local language (if different) is required. Strong communication and collaboration skills in multidisciplinary and regulated environments. Benefits: Opportunity to work at the forefront of medical device safety and regulatory science. Exposure to global standards and internationally recognized regulatory frameworks. Collaborative, science-driven work environment focused on innovation and patient safety. Professional development within a highly specialized and regulated industry. Chance to contribute to medical technologies that directly improve healthcare outcomes worldwide. Competitive compensation and benefits package (based on location and experience). ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Biological Safety Specialist. Skills: Biological safety, Regulatory compliance, Medical device safety. Develop biological safety documentation. 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Our partner is looking for a Biological Safety Specialist based in Spain. This role sits at the intersection of science, regulation, and medical device innovation, ensuring that products meet the highest standards of biological safety throughout their development lifecycle. You will contribute directly to the safety and compliance of medical technologies that impact patient health globally. Working within a highly specialized and regulated environment, you will evaluate scientific data, assess biocompatibility, and support the creation of critical regulatory documentation. The position involves close collaboration with multidisciplinary teams and external stakeholders to ensure alignment with international standards. You will play a key role in shaping safety assessments that influence product approval and market readiness. This is a detail-driven and impact-focused role suited for professionals passionate about science, compliance, and healthcare innovation. ## Accountabilities Develop, review, and maintain biological safety documentation and reports in compliance with applicable international standards and medical device regulations. Assess and audit biocompatibility and material characterization data to ensure alignment with regulatory requirements and safety expectations. Interpret complex scientific and technical information to support risk assessments and regulatory submissions for medical devices. Collaborate with cross-functional teams to ensure biological safety considerations are integrated throughout the product development lifecycle. Review and contribute to the development of complex technical and regulatory documents with a high level of accuracy and scientific rigor. Support continuous improvement of biological safety processes, methodologies, and compliance frameworks. Requirements: Bachelor’s degree with at least 5 years of relevant experience, or Master’s/Doctorate degree with at least 2 years of relevant experience in a scientific or related discipline. Strong knowledge of medical device regulations and international standards related to biological safety and biocompatibility. Experience assessing compliance of biocompatibility studies and material characterization against regulatory requirements. Proven ability to write, review, and manage complex technical and regulatory documentation. Strong analytical and critical thinking skills with attention to detail and scientific accuracy. Proficiency in Microsoft Word and other standard documentation tools. Fluency in English; proficiency in the local language (if different) is required. Strong communication and collaboration skills in multidisciplinary and regulated environments. Benefits: Opportunity to work at the forefront of medical device safety and regulatory science. Exposure to global standards and internationally recognized regulatory frameworks. Collaborative, science-driven work environment focused on innovation and patient safety. Professional development within a highly specialized and regulated industry. Chance to contribute to medical technologies that directly improve healthcare outcomes worldwide. Competitive compensation and benefits package (based on location and experience). ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Biological Safety Specialist. Skills: Biological safety, Biocompatibility, Regulatory documentation. Develop biological safety documentation. Review biological safety documentation", "postedDate" : "2026-06-09T11:49:44.346", "createdAt" : "2026-06-09T11:49:44.346", "lastUpdated" : "2026-06-15T22:10:18.192", "ingestTimestamp" : "2026-06-14T21:15:15.947", "mongoId" : "6a2cb20774d8ee00a09def4c", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ "Material characterization", "Scientific rigor", "Biological safety", "Biocompatibility", "Regulatory documentation", "Risk assessment", "Regulatory submissions", "Medical device regulations", "International standards", "Medical technologies", "Microsoft Word" ], "skillCount" : 11, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 0.8888889, "daysOld" : 6, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2cb20774d8ee00a09def4f", "title" : "Biological Safety Specialist", "industry" : "Legal", "salary" : { "min" : 65000.0, "max" : 95000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Biological Safety Specialist in the Biotech industry in the Netherlands, adjusted for seniority and city tier." }, "location" : "Netherlands", "locations" : [ "Netherlands" ], "timestamp" : "2026-06-16T01:32:11.837", "fingerprint" : "b7b52d30eff4cb5ee47c203a2008a9071e17d4c6e6e5673070d135c7cbef5e42", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/jobgether/bc10188a-3334-4368-8dd2-ef976c2037dc/apply", "externalId" : "bc10188a-3334-4368-8dd2-ef976c2037dc", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Netherlands", "continent" : "eu", "workMode" : "onsite" } ], "locationText" : "Netherlands", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 2, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Regulatory submissions", "Risk assessments", "Material characterization" ], "hardSkillsList" : [ "Biological safety documentation", "Biocompatibility data assessment", "Scientific rigor" ], "hardSkills" : [ { "name" : "Biological safety documentation", "level" : "intermediate" }, { "name" : "Biocompatibility data assessment", "level" : "intermediate" }, { "name" : "Scientific rigor", "level" : "intermediate" } ], "majorSkills" : "Biological safety, Medical device regulations, Biocompatibility", "majorSkillsList" : [ "Biological safety", "Medical device regulations", "Biocompatibility" ], "coreResponsibilities" : "Develop biological safety documentation, Review biological safety documentation, Maintain biological safety documentation, Assess biocompatibility data, Audit biocompatibility data, Assess material characterization data, Audit material characterization data, Interpret scientific information, Interpret technical information, Support risk assessments, Support regulatory submissions, Integrate biological safety considerations, Contribute to technical documents, Contribute to regulatory documents, Support process improvement, Support methodology improvement, Support compliance framework improvement", "teamCollaboration" : "Cross-functional teams", "domainKnowledge" : "Medical device regulations; Biological safety; Biocompatibility; Material characterization", "domainList" : [ "medical-device-regulations", "biological-safety", "biocompatibility", "material-characterization" ], "domainSpecificKnowledge" : [ "Medical device regulations", "Biological safety", "Biocompatibility", "Material characterization" ], "toolProficiency" : [ "Microsoft Word" ], "documentationSkills" : "Technical documentation; Regulatory documentation", "problemSolvingSkills" : "Analytical thinking; Critical thinking", "qualificationsBasic" : "Bachelor's degree with 5 years experience, Master's/Doctorate degree with 2 years experience, Knowledge of medical device regulations, Knowledge of international standards, Experience assessing biocompatibility studies, Experience assessing material characterization, Proven ability to write documentation, Proven ability to review documentation, Proven ability to manage documentation, Analytical and critical thinking skills, Proficiency in Microsoft Word, Proficiency in standard documentation tools, Fluency in local language", "qualificationsPreferred" : "Master's degree with 2 years experience, Doctorate degree with 2 years experience", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Accountabilities Develop, review, and maintain biological safety documentation and reports in compliance with applicable international standards and medical device regulations. Assess and audit biocompatibility and material characterization data to ensure alignment with regulatory requirements and safety expectations. Interpret complex scientific and technical information to support risk assessments and regulatory submissions for medical devices. Collaborate with cross-functional teams to ensure biological safety considerations are integrated throughout the product development lifecycle. Review and contribute to the development of complex technical and regulatory documents with a high level of accuracy and scientific rigor. Support continuous improvement of biological safety processes, methodologies, and compliance frameworks. Requirements: Bachelor’s degree with at least 5 years of relevant experience, or Master’s/Doctorate degree with at least 2 years of relevant experience in a scientific or related discipline. Strong knowledge of medical device regulations and international standards related to biological safety and biocompatibility. Experience assessing compliance of biocompatibility studies and material characterization against regulatory requirements. Proven ability to write, review, and manage complex technical and regulatory documentation. Strong analytical and critical thinking skills with attention to detail and scientific accuracy. Proficiency in Microsoft Word and other standard documentation tools. Fluency in English; proficiency in the local language (if different) is required. Strong communication and collaboration skills in multidisciplinary and regulated environments. Benefits: Opportunity to work at the forefront of medical device safety and regulatory science. Exposure to global standards and internationally recognized regulatory frameworks. Collaborative, science-driven work environment focused on innovation and patient safety. Professional development within a highly specialized and regulated industry. Chance to contribute to medical technologies that directly improve healthcare outcomes worldwide. Competitive compensation and benefits package (based on location and experience). ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Biological Safety Specialist. Skills: Biological safety, Medical device regulations, Biocompatibility. Develop biological safety documentation. 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Assess and audit biocompatibility and material characterization data to ensure alignment with regulatory requirements and safety expectations. Interpret complex scientific and technical information to support risk assessments and regulatory submissions for medical devices. Collaborate with cross-functional teams to ensure biological safety considerations are integrated throughout the product development lifecycle. Review and contribute to the development of complex technical and regulatory documents with a high level of accuracy and scientific rigor. Support continuous improvement of biological safety processes, methodologies, and compliance frameworks. Requirements: Bachelor’s degree with at least 5 years of relevant experience, or Master’s/Doctorate degree with at least 2 years of relevant experience in a scientific or related discipline. Strong knowledge of medical device regulations and international standards related to biological safety and biocompatibility. Experience assessing compliance of biocompatibility studies and material characterization against regulatory requirements. Proven ability to write, review, and manage complex technical and regulatory documentation. Strong analytical and critical thinking skills with attention to detail and scientific accuracy. Proficiency in Microsoft Word and other standard documentation tools. Fluency in English; proficiency in the local language (if different) is required. Strong communication and collaboration skills in multidisciplinary and regulated environments. Benefits: Opportunity to work at the forefront of medical device safety and regulatory science. Exposure to global standards and internationally recognized regulatory frameworks. Collaborative, science-driven work environment focused on innovation and patient safety. Professional development within a highly specialized and regulated industry. Chance to contribute to medical technologies that directly improve healthcare outcomes worldwide. Competitive compensation and benefits package (based on location and experience). ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Biological Safety Specialist. Skills: Biological safety, Medical device regulations, Biocompatibility. Develop biological safety documentation. 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Assess and audit biocompatibility and material characterization data to ensure alignment with regulatory requirements and safety expectations. Interpret complex scientific and technical information to support risk assessments and regulatory submissions for medical devices. Collaborate with cross-functional teams to ensure biological safety considerations are integrated throughout the product development lifecycle. Review and contribute to the development of complex technical and regulatory documents with a high level of accuracy and scientific rigor. Support continuous improvement of biological safety processes, methodologies, and compliance frameworks. Requirements: Bachelor’s degree with at least 5 years of relevant experience, or Master’s/Doctorate degree with at least 2 years of relevant experience in a scientific or related discipline. Strong knowledge of medical device regulations and international standards related to biological safety and biocompatibility. 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Chance to contribute to medical technologies that directly improve healthcare outcomes worldwide. Competitive compensation and benefits package (based on location and experience). ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Biological Safety Specialist. Skills: Biological safety, Biocompatibility, Regulatory compliance. Develop biological safety documentation. 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Chance to contribute to medical technologies that directly improve healthcare outcomes worldwide. Competitive compensation and benefits package (based on location and experience). ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. 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Assess and audit biocompatibility and material characterization data to ensure alignment with regulatory requirements and safety expectations. Interpret complex scientific and technical information to support risk assessments and regulatory submissions for medical devices. Collaborate with cross-functional teams to ensure biological safety considerations are integrated throughout the product development lifecycle. Review and contribute to the development of complex technical and regulatory documents with a high level of accuracy and scientific rigor. Support continuous improvement of biological safety processes, methodologies, and compliance frameworks. Requirements: Bachelor’s degree with at least 5 years of relevant experience, or Master’s/Doctorate degree with at least 2 years of relevant experience in a scientific or related discipline. Strong knowledge of medical device regulations and international standards related to biological safety and biocompatibility. Experience assessing compliance of biocompatibility studies and material characterization against regulatory requirements. Proven ability to write, review, and manage complex technical and regulatory documentation. Strong analytical and critical thinking skills with attention to detail and scientific accuracy. Proficiency in Microsoft Word and other standard documentation tools. Fluency in English; proficiency in the local language (if different) is required. Strong communication and collaboration skills in multidisciplinary and regulated environments. Benefits: Opportunity to work at the forefront of medical device safety and regulatory science. Exposure to global standards and internationally recognized regulatory frameworks. Collaborative, science-driven work environment focused on innovation and patient safety. Professional development within a highly specialized and regulated industry. Chance to contribute to medical technologies that directly improve healthcare outcomes worldwide. Competitive compensation and benefits package (based on location and experience). ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Biological Safety Specialist. Skills: Biological safety, Medical device regulations, Biocompatibility. Develop biological safety documentation. Review biological safety documentation", "postedDate" : "2026-06-09T11:47:12.169", "createdAt" : "2026-06-09T11:47:12.169", "lastUpdated" : "2026-06-16T00:35:42.592", "ingestTimestamp" : "2026-06-14T22:14:12.388", "mongoId" : "6a2cb20774d8ee00a09def56", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "50k-75k", "hasSalary" : false, "allSkills" : [ "Biological safety documentation", "Biological safety reports", "Biocompatibility studies", "Material characterization", "Analytical thinking", "Critical thinking", "Biological safety", "Medical device regulations", "Biocompatibility", "Risk assessment", "Regulatory submissions", "International standards", "Microsoft Word" ], "skillCount" : 13, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Mid", "dataQualityScore" : 0.8888889, "daysOld" : 6, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a305a5cf292fd229cf4f99c", "title" : "Performance Manager", "company" : "AutoTrader.ca", "industry" : "Technology", "salary" : { "min" : 65000.0, "max" : 75000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Trader Corporation", "locations" : [ "Trader Corporation" ], "timestamp" : "2026-06-16T08:24:14.807", "fingerprint" : "a091a39c2206f8ee55661fa29ee6664ed16e529fce8d07b8822f8f90858a399a", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/autotradercanada/jobs/7768418003", "externalId" : "7768418003", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Canada", "continent" : "na", "workMode" : "onsite" } ], "locationText" : "Canada", "employmentType" : "FULL_TIME", "minimumEducation" : "High School", "experienceLevel" : "Manager", "professionalSkills" : [ "Performance management", "Program compliance", "Operational excellence", "Data-driven insights", "Sales initiatives support" ], "hardSkillsList" : [ "Data analysis", "Performance analysis" ], "hardSkills" : [ { "name" : "Data analysis", "level" : "intermediate" }, { "name" : "Performance analysis", "level" : "intermediate" } ], "majorSkills" : "Dealer relationship management, Program adoption, Performance analysis", "majorSkillsList" : [ "Dealer relationship management", "Program adoption", "Performance analysis" ], "coreResponsibilities" : "Onboard new dealer partners, Ensure smooth launch experience, Ensure successful launch experience, Monitor dealer compliance, Support dealer compliance, Provide guidance on compliance, Provide recommendations on compliance, Build relationships with dealer partners, Maintain relationships with dealer partners, Analyze program performance data, Analyze dealer performance data, Deliver insights for business decisions, Deliver insights for sales initiatives, Collaborate with sales teams, Collaborate with cross-functional teams, Improve processes, Drive adoption, Contribute to ICO program success", "teamCollaboration" : "Internal stakeholders; Sales teams; Cross-functional teams", "domainKnowledge" : "Automotive industry; Dealership operations; Vehicle acquisition processes; Digital automotive solutions", "domainList" : [ "automotive-industry", "dealership-operations", "vehicle-acquisition-processes", "digital-automotive-solutions" ], "domainSpecificKnowledge" : [ "Automotive industry", "Dealership operations", "Vehicle acquisition processes", "Digital automotive solutions" ], "communicationSkills" : "Effective communication", "continuousLearning" : "Conferences and training budget; Regular internal training programs", "problemSolvingSkills" : "Problem-solving skills; Interpret data; Translate insights into action", "outcomesObjectives" : "Drive growth; Drive engagement", "qualificationsBasic" : "Automotive industry experience, Dealership operations understanding, Dealer business needs understanding, Vehicle acquisition processes knowledge, Factors influencing dealer purchasing decisions knowledge, Build relationships ability, Communicate effectively virtual environment ability, Analytical skills, Problem-solving skills, Interpret data ability, Translate insights into action ability, High school diploma or equivalent, Quickly learn new systems ability, Quickly learn new tools ability, Quickly learn new technologies ability", "rawDescription" : "We are a Canadian leader in digital automotive solutions. Our flagship brands — AutoTrader.ca, AutoSync, Dealertrack Canada and CMS — help Canadians buy, sell, and finance vehicles with confidence. AutoTrader.ca is Canada’s largest automotive marketplace, with over 25 million monthly visits. Through AutoSync, we provide software solutions to 3,500+ dealers, streamlining their operations, marketing, and sales. Dealertrack Canada is the country’s top automotive financing portal, processing more than 6.5 million credit applications each year. Collateral Management (CMS) is a national tech solution that boosts lien and registration services, recovery services, and insolvency management solutions for Canadian Lenders. As part of AutoScout24 group, Europe’s largest online car marketplace, we’re shaping the future of automotive retail in Canada and beyond. Join us on our journey as we bring together the best of Europe and North America to shape the future of automotive retail. What you’ll do The Performance Management team supports the success of our Instant Cash Offer (ICO) program by helping dealer partners onboard, adopt, and maximize the value of the platform. As a Performance Manager, you’ll work closely with dealers and internal stakeholders to ensure program compliance, support operational excellence, and provide data-driven insights that help drive growth and engagement. Onboard new dealer partners to the Instant Cash Offer program, ensuring a smooth and successful launch experience. Monitor and support dealer compliance with program requirements, providing guidance and recommendations as needed. Build and maintain strong relationships with a dedicated portfolio of dealer partners Analyze program and dealer performance data, delivering insights that support business decisions and sales team initiatives. Collaborate with sales and cross-functional teams to improve processes, drive adoption, and contribute to the ongoing success of the ICO program. What you’ll bring Experience working in the automotive industry, with a strong understanding of dealership operations and dealer business needs. Knowledge of vehicle acquisition processes and the factors that influence dealer purchasing decisions. Proven ability to build relationships and communicate effectively in a virtual environment. Strong analytical and problem-solving skills, with the ability to interpret data and translate insights into action. High school diploma or equivalent, along with the ability to quickly learn new systems, tools, and technologies. What’s in it for you We understand that there is life at work and life outside of work. Here are a few benefits we all benefit from that support us to be our creative best. Benefits from Day 1 Gym discounts Employee and Family Assistance program Virtual wellness events Conferences & training budget Regular internal training programs Financial planning Let us help you invest in your future with 3% matching towards your pension and multiple forms of income protection. Compensation The expected compensation for this position is: CAD $65,000 to $75,000 For a career where you can drive our business and shape your future, apply now. Compensation Our ranges reflect the expected compensation at the time of posting. The final offer may vary and can be higher based on relevant skills, experience, location, and market conditions. Based on the role, the total rewards package may also include benefits, bonus, and other employee offerings. The base salary range for this position is $65,000—$75,000 CAD Use of Artificial Intelligence in Hiring: We use artificial intelligence (“AI”) in our hiring process, including to screen, assess, or select applicants for this position. Vacancy Status: This job posting is for an existing vacancy.", "summaryDescription" : "Performance Manager at AutoTrader.ca. Skills: Dealer relationship management, Program adoption, Performance analysis. Onboard new dealer partners. Ensure smooth launch experience", "postedDate" : "2026-06-15T23:25:11.815", "createdAt" : "2026-06-15T23:25:11.815", "lastUpdated" : "2026-06-16T08:24:14.807", "ingestTimestamp" : "2026-06-15T23:25:11.815", "mongoId" : "6a305a5cf292fd229cf4f99c", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "50k-75k", "hasSalary" : false, "allSkills" : [ "Data analysis", "Performance analysis", "Dealer relationship management", "Program adoption", "Performance management", "Program compliance", "Operational excellence", "Data-driven insights", "Sales initiatives support", "Automotive industry", "Dealership operations", "Vehicle acquisition processes", "Digital automotive solutions" ], "skillCount" : 13, "jobCategory" : "sales", "jobSubcategory" : "revenue", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Automotive", "llmIndustryConfidence" : 0.92 }, { "id" : "6a2ca6d474d8ee00a09bcfd6", "title" : "Regional Sales Manager ARGENTINA – Biological Products (B2B)", "company" : "Lesaffre", "industry" : "Farming", "salary" : { "min" : 1.05E7, "max" : 1.65E7, "currency" : "ARS", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Manager-level Regional Sales Manager in the Biotech industry in Buenos Aires, Argentina, adjusted for seniority and company size." }, "location" : "Buenos Aires, Buenos Aires, AR", "locations" : [ "Buenos Aires", "Buenos Aires", "AR" ], "timestamp" : "2026-06-16T06:15:22.654", "fingerprint" : "e66918bd701517b589f609349ddaa1467362efa5337c69a483a4e60772911f20", "source" : "smartrecruiters", "language" : "es", "applyUrl" : "https://jobs.smartrecruiters.com/Lesaffre/744000131749129-regional-sales-manager-argentina-biological-products-b2b-", "externalId" : "744000131749129", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Buenos Aires", "state" : "Buenos Aires", "country" : "Argentina", "continent" : "sa", "source" : "llm", "workMode" : "onsite", "geo" : "-34.5121516,-58.5248182" } ], "locationText" : "Buenos Aires, Buenos Aires, Argentina", "employmentType" : "FULL_TIME", "minimumEducation" : "Agricultural Engineer", "experienceMinYears" : 15, "experienceMaxYears" : 99, "experienceLevel" : "executive", "professionalSkills" : [ "P&L management", "Commercial planning", "Distributor network management", "Market positioning" ], "hardSkillsList" : [ "Sales forecasting", "Profitability analysis", "Agronomic positioning" ], "hardSkills" : [ { "name" : "Sales forecasting", "level" : "intermediate" }, { "name" : "Profitability analysis", "level" : "intermediate" }, { "name" : "Agronomic positioning", "level" : "intermediate" } ], "majorSkills" : "Sales management, Business development, Distribution management", "majorSkillsList" : [ "Sales management", "Business development", "Distribution management" ], "coreResponsibilities" : "Deliver sales targets, Deliver market share targets, Deliver profitability targets, Own subregional P&L, Manage subregional P&L, Ensure profitable business growth, Adapt biological products portfolio, Develop annual commercial plans, Execute annual commercial plans, Build distributor network, Manage distributor network, Develop distributor network, Evaluate distributor performance, Recommend distributor changes, Identify new strategic distributors, Onboard new strategic distributors, Develop relationships with key customers, Develop relationships with strategic accounts, Ensure marketing campaign implementation, Ensure product launch implementation, Work closely with technical team, Coordinate with local teams, Consolidate commercial information", "teamCollaboration" : "Marketing manager; Regional technical team; Local teams in Argentina; Local teams in Brazil; Local teams in Latin America; Sales teams; Headquarters", "domainKnowledge" : "Biological products; Biofertilizers; Inoculants; Biostimulants; Biocontrol; Agronomic realities; Extensive crops; Intensive crops; Fermentation", "domainList" : [ "biological-products", "biofertilizers", "inoculants", "biostimulants", "biocontrol", "agronomic-realities", "extensive-crops", "intensive-crops", "fermentation" ], "domainSpecificKnowledge" : [ "Biological products", "Biofertilizers", "Inoculants", "Biostimulants", "Biocontrol", "Agronomic realities", "Extensive crops", "Intensive crops", "Fermentation" ], "continuousLearning" : "Continuous improvement mindset; Learning opportunities", "outcomesObjectives" : "Sustainable business growth; Profitable business growth", "qualificationsBasic" : "Agricultural Engineer (mandatory), 5+ years in commercial positions, Experience in biological products, Experience working with B2B distribution channels, Regional experience in Latin America, Advanced or native Spanish, Advanced or native English", "qualificationsPreferred" : "French (optional), Portuguese (optional)", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Como actor global clave en el ámbito de las levaduras y la fermentación , Lesaffre diseña, fabrica y comercializa soluciones innovadoras para los sectores de Panificación, Sabor y Placer Alimentario, Salud y Biotecnología. Fundado en 1853 como un grupo familiar en el norte de Francia, Lesaffre se ha convertido en una empresa multinacional y multicultural, comprometida con trabajar con confianza para alimentar y proteger mejor el planeta. En estrecha colaboración con sus clientes y socios, Lesaffre cuenta con más de 11.000 colaboradores en más de 50 países. La empresa alcanza una facturación de 3 mil millones de euros. * Deliver sales, market share and profitability targets for the assigned territory. * Own and manage the subregional P&L, ensuring sustainable and profitable business growth. * Adapt the biological products portfolio to local agronomic realities. * Develop and execute annual commercial plans aligned with regional strategy. * Build, manage and develop a high-performing distributor network. * Evaluate distributor performance and recommend changes, additions or restructuring when necessary. * Identify and onboard new strategic distributors aligned with long-term business objectives. * Develop strong relationships with key customers and strategic accounts * Ensure the effective implementation of marketing campaigns and product launches with the assistant of the marketing manager. * Work closely with the regional technical team to ensure strong agronomic positioning of the portfolio. * Work with technical institutions and local consultants. * Coordinate with local teams in Argentina, Brazil, and the rest of Latin America. * Consolidate existing commercial information in the region for sales teams and headquarters. ## Qualifications Education • Agricultural Engineer (mandatory). Experience • 5+ years in commercial positions within the agricultural sector. • Experience in biological products (biofertilizers, inoculants, biostimulants, biocontrol). • Experience working with B2B distribution channels. • Regional experience in Latin America, preferably in extensive crops but also in intensive crops. Knowledge • Knowledge in biofertilizers, inoculants, bioestimulants, biocontrol). Technical Skills • Advanced or native Spanish and English (mandatory). • French and Portugues (optional) Behavioral Skills * Proactive, guided to results, autonomous Core Competencies Lesaffre * Support individual & people development Ability to guide & support teams members’ growth by identifying development needs, providing constructive feedback, and creating opportunities for learning. Empowers individuals to build their skills. * Deal with complexity, uncertainty & ambiguity Able to explain complex situation in a simple way and maintain stable performance under complexity, uncertainty & ambiguity. * Manage team’s efficiency & energy Motivate own team to maximize efficiency by setting a clear purpose, relevant objectives to the team and create an energizing environment. * Manage changes Manage the implementation and acceptance of change. Address change resistance. * Lead by example Maintain a professional attitude in all circumstances (assume failures, show courage, show fairness…). * For all Employees at Lesaffre Show curiosity & Open mind, show a continuous improvement mindset, show initiative & focus on priorities, strive for results & performance and Promote cooperation, collaboration & company spirit ## Additional Information Te ofrecemos un entorno laboral pensado para tu bienestar: Beneficios: * Comedor en Oficinas – Opciones variadas para una alimentación saludable y cómoda. * Obra social para tu grupo familiar – Protegemos tu bienestar y el de los tuyos. * Vacaciones extendidas – A partir de los 3 años, accedé a 21 días corridos de descanso. * Bono anual – Reconocemos tu compromiso con una recompensa especial. * Bonda Plataforma de descuentos exclusivos – Accede a beneficios especiales en distintos rubros pensados solo para vos. * Programa de Bienestar – Plataforma de asistencia Psicológica y Legal gratuita al Colaborador. * Día del Cumpleaños Libre – Disfruta tu día como más te guste. Únete a una empresa familiar con una larga trayectoria y valores centrados en las personas, con una misión clara: Nutrir y Proteger nuestro Planeta. Podrás desarrollar tu carrera en un entorno de trabajo enriquecedor y en un contexto multicultural que promueve el aprendizaje continuo y la colaboración. Te ofrecemos un entorno laboral pensado para tu bienestar: En Lesaffre, la diversidad es una fortaleza que enriquece nuestra cultura y nuestros equipos. Estamos comprometidos con ofrecerte un entorno laboral donde puedas desarrollarte plenamente, sin importar tu origen, género, edad o capacidades. Valoramos todas las candidaturas, porque creemos que las perspectivas diversas fortalecen nuestra capacidad de innovar y enfrentar los desafíos del futuro. Gracias por tu interés en formar parte de nuestro equipo: Queremos que estés al tanto de cada etapa del proceso de selección, para que sepas qué esperar y cómo prepararte. A continuación, te detallamos los pasos que seguimos: Filtro de CV Evaluamos tu perfil en función de los requisitos del puesto. Entrevista con Recursos Humanos Una charla inicial para conocerte, contarte más sobre la empresa y el rol, y despejar dudas. Entrevista con la Gerencia Reunión con el responsable del área para profundizar en tu experiencia y expectativas. Evaluación de perfil Diseñada conforme las competencias requeridas para el puesto. Examen preocupacional Evaluación médica obligatoria previa al ingreso. Envío de carta oferta Recibirás nuestra propuesta formal para sumarte al equipo. La duración estimada de todo el proceso de selección es de aproximadamente 3 semanas desde el contacto inicial.", "summaryDescription" : "Regional Sales Manager ARGENTINA – Biological Products (B2B) at Lesaffre. Skills: Sales management, Business development, Distribution management. Deliver sales targets. Deliver market share targets", "postedDate" : "2026-06-11T19:35:09.000", "createdAt" : "2026-06-14T19:34:14.802", "lastUpdated" : "2026-06-16T06:15:22.654", "ingestTimestamp" : "2026-06-14T19:34:14.802", "mongoId" : "6a2ca6d474d8ee00a09bcfd6", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Sales forecasting", "Profitability analysis", "Agronomic positioning", "Sales management", "Business development", "Distribution management", "P&L management", "Commercial planning", "Distributor network management", "Market positioning", "Biological products", "Biofertilizers", "Inoculants", "Biostimulants", "Biocontrol", "Agronomic realities", "Extensive crops", "Intensive crops", "Fermentation" ], "skillCount" : 19, "jobCategory" : "sales", "jobSubcategory" : "revenue", "seniorityLevel" : "Manager", "dataQualityScore" : 1.0, "daysOld" : 4, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c652974d8ee00a08fca11", "title" : "Regional Sales Manager ARGENTINA – Biological Products (B2B)", "company" : "Lesaffre", "industry" : "Farming", "salary" : { "min" : 1.1E7, "max" : 1.8E7, "currency" : "ARS", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Manager-level Regional Sales Manager in Buenos Aires, Argentina within the Biotech industry, adjusted for seniority and company size." }, "location" : "Buenos Aires, Buenos Aires, AR", "locations" : [ "Buenos Aires", "Buenos Aires", "AR" ], "timestamp" : "2026-06-15T07:53:24.575", "fingerprint" : "7902b65175d7caae1ab56fc230020a668c24c8e258dd6c65988d3d63a0485e6a", "source" : "smartrecruiters", "language" : "es", "applyUrl" : "https://jobs.smartrecruiters.com/Lesaffre/744000131749129-regional-sales-manager-argentina-biological-products-b2b-", "externalId" : "744000131749129", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Buenos Aires", "state" : "Buenos Aires", "country" : "Argentina", "continent" : "sa", "source" : "llm", "workMode" : "onsite", "geo" : "-34.5121516,-58.5248182" } ], "locationText" : "Buenos Aires, Buenos Aires, Argentina", "employmentType" : "FULL_TIME", "minimumEducation" : "Agricultural Engineer", "experienceMinYears" : 15, "experienceMaxYears" : 99, "experienceLevel" : "executive", "professionalSkills" : [ "Market share", "Profitability targets", "Business growth", "Commercial plans", "Product launches", "Agronomic positioning" ], "hardSkillsList" : [ "P&L management", "Distributor network management", "Customer relationship management" ], "softSkillsList" : [ "Autonomous", "Curiosity", "Open mind", "Continuous improvement", "Initiative", "Focus on priorities", "Promote cooperation", "Company spirit" ], "hardSkills" : [ { "name" : "P&L management", "level" : "intermediate" }, { "name" : "Distributor network management", "level" : "intermediate" }, { "name" : "Customer relationship management", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Autonomous" }, { "name" : "Curiosity" }, { "name" : "Open mind" }, { "name" : "Continuous improvement" }, { "name" : "Initiative" }, { "name" : "Focus on priorities" }, { "name" : "Promote cooperation" }, { "name" : "Company spirit" } ], "majorSkills" : "Sales management, Biological products, Distribution channels", "majorSkillsList" : [ "Sales management", "Biological products", "Distribution channels" ], "coreResponsibilities" : "Deliver sales targets, Deliver market share targets, Deliver profitability targets, Own subregional P&L, Manage subregional P&L, Ensure profitable business growth, Adapt biological products portfolio, Develop annual commercial plans, Execute annual commercial plans, Build distributor network, Manage distributor network, Develop distributor network, Evaluate distributor performance, Recommend distributor changes, Recommend distributor additions, Recommend distributor restructuring, Identify new strategic distributors, Onboard new strategic distributors, Develop relationships with key customers, Develop relationships with strategic accounts, Ensure marketing campaign implementation, Ensure product launch implementation, Work closely with technical team, Ensure agronomic positioning, Work with technical institutions, Work with local consultants, Coordinate with local teams, Consolidate commercial information", "teamCollaboration" : "Marketing manager; Regional technical team; Local teams Argentina; Local teams Brazil; Local teams Latin America; Sales teams; Headquarters", "domainKnowledge" : "Biological products; Biofertilizers; Inoculants; Biostimulants; Biocontrol; Agronomic realities; Extensive crops; Intensive crops", "domainList" : [ "biological-products", "biofertilizers", "inoculants", "biostimulants", "biocontrol", "agronomic-realities", "extensive-crops", "intensive-crops" ], "domainSpecificKnowledge" : [ "Biological products", "Biofertilizers", "Inoculants", "Biostimulants", "Biocontrol", "Agronomic realities", "Extensive crops", "Intensive crops" ], "communicationSkills" : "Consolidate commercial information", "continuousLearning" : "Continuous learning", "outcomesObjectives" : "Sustainable business growth; Profitable business growth", "qualificationsBasic" : "Agricultural Engineer, 5+ years in commercial positions, Experience in biological products, Experience working with B2B distribution channels, Regional experience in Latin America, Advanced or native Spanish, Advanced or native English", "qualificationsPreferred" : "French language proficiency, Portuguese language proficiency, Experience in extensive crops, Experience in intensive crops", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Como actor global clave en el ámbito de las levaduras y la fermentación , Lesaffre diseña, fabrica y comercializa soluciones innovadoras para los sectores de Panificación, Sabor y Placer Alimentario, Salud y Biotecnología. Fundado en 1853 como un grupo familiar en el norte de Francia, Lesaffre se ha convertido en una empresa multinacional y multicultural, comprometida con trabajar con confianza para alimentar y proteger mejor el planeta. En estrecha colaboración con sus clientes y socios, Lesaffre cuenta con más de 11.000 colaboradores en más de 50 países. La empresa alcanza una facturación de 3 mil millones de euros. * Deliver sales, market share and profitability targets for the assigned territory. * Own and manage the subregional P&L, ensuring sustainable and profitable business growth. * Adapt the biological products portfolio to local agronomic realities. * Develop and execute annual commercial plans aligned with regional strategy. * Build, manage and develop a high-performing distributor network. * Evaluate distributor performance and recommend changes, additions or restructuring when necessary. * Identify and onboard new strategic distributors aligned with long-term business objectives. * Develop strong relationships with key customers and strategic accounts * Ensure the effective implementation of marketing campaigns and product launches with the assistant of the marketing manager. * Work closely with the regional technical team to ensure strong agronomic positioning of the portfolio. * Work with technical institutions and local consultants. * Coordinate with local teams in Argentina, Brazil, and the rest of Latin America. * Consolidate existing commercial information in the region for sales teams and headquarters. ## Qualifications Education • Agricultural Engineer (mandatory). Experience • 5+ years in commercial positions within the agricultural sector. • Experience in biological products (biofertilizers, inoculants, biostimulants, biocontrol). • Experience working with B2B distribution channels. • Regional experience in Latin America, preferably in extensive crops but also in intensive crops. Knowledge • Knowledge in biofertilizers, inoculants, bioestimulants, biocontrol). Technical Skills • Advanced or native Spanish and English (mandatory). • French and Portugues (optional) Behavioral Skills * Proactive, guided to results, autonomous Core Competencies Lesaffre * Support individual & people development Ability to guide & support teams members’ growth by identifying development needs, providing constructive feedback, and creating opportunities for learning. Empowers individuals to build their skills. * Deal with complexity, uncertainty & ambiguity Able to explain complex situation in a simple way and maintain stable performance under complexity, uncertainty & ambiguity. * Manage team’s efficiency & energy Motivate own team to maximize efficiency by setting a clear purpose, relevant objectives to the team and create an energizing environment. * Manage changes Manage the implementation and acceptance of change. Address change resistance. * Lead by example Maintain a professional attitude in all circumstances (assume failures, show courage, show fairness…). * For all Employees at Lesaffre Show curiosity & Open mind, show a continuous improvement mindset, show initiative & focus on priorities, strive for results & performance and Promote cooperation, collaboration & company spirit ## Additional Information Te ofrecemos un entorno laboral pensado para tu bienestar: Beneficios: * Comedor en Oficinas – Opciones variadas para una alimentación saludable y cómoda. * Obra social para tu grupo familiar – Protegemos tu bienestar y el de los tuyos. * Vacaciones extendidas – A partir de los 3 años, accedé a 21 días corridos de descanso. * Bono anual – Reconocemos tu compromiso con una recompensa especial. * Bonda Plataforma de descuentos exclusivos – Accede a beneficios especiales en distintos rubros pensados solo para vos. * Programa de Bienestar – Plataforma de asistencia Psicológica y Legal gratuita al Colaborador. * Día del Cumpleaños Libre – Disfruta tu día como más te guste. Únete a una empresa familiar con una larga trayectoria y valores centrados en las personas, con una misión clara: Nutrir y Proteger nuestro Planeta. Podrás desarrollar tu carrera en un entorno de trabajo enriquecedor y en un contexto multicultural que promueve el aprendizaje continuo y la colaboración. Te ofrecemos un entorno laboral pensado para tu bienestar: En Lesaffre, la diversidad es una fortaleza que enriquece nuestra cultura y nuestros equipos. Estamos comprometidos con ofrecerte un entorno laboral donde puedas desarrollarte plenamente, sin importar tu origen, género, edad o capacidades. Valoramos todas las candidaturas, porque creemos que las perspectivas diversas fortalecen nuestra capacidad de innovar y enfrentar los desafíos del futuro. Gracias por tu interés en formar parte de nuestro equipo: Queremos que estés al tanto de cada etapa del proceso de selección, para que sepas qué esperar y cómo prepararte. A continuación, te detallamos los pasos que seguimos: Filtro de CV Evaluamos tu perfil en función de los requisitos del puesto. Entrevista con Recursos Humanos Una charla inicial para conocerte, contarte más sobre la empresa y el rol, y despejar dudas. Entrevista con la Gerencia Reunión con el responsable del área para profundizar en tu experiencia y expectativas. Evaluación de perfil Diseñada conforme las competencias requeridas para el puesto. Examen preocupacional Evaluación médica obligatoria previa al ingreso. Envío de carta oferta Recibirás nuestra propuesta formal para sumarte al equipo. La duración estimada de todo el proceso de selección es de aproximadamente 3 semanas desde el contacto inicial.", "summaryDescription" : "Regional Sales Manager ARGENTINA – Biological Products (B2B) at Lesaffre. Skills: Sales management, Biological products, Distribution channels. Deliver sales targets. Deliver market share targets", "postedDate" : "2026-06-11T19:35:09.000", "createdAt" : "2026-06-13T16:51:04.107", "lastUpdated" : "2026-06-15T07:53:24.575", "ingestTimestamp" : "2026-06-13T16:51:04.107", "mongoId" : "6a2c652974d8ee00a08fca11", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "P&L management", "Distributor network management", "Customer relationship management", "Autonomous", "Curiosity", "Open mind", "Continuous improvement", "Initiative", "Focus on priorities", "Promote cooperation", "Company spirit", "Sales management", "Biological products", "Distribution channels", "Market share", "Profitability targets", "Business growth", "Commercial plans", "Product launches", "Agronomic positioning", "Biofertilizers", "Inoculants", "Biostimulants", "Biocontrol", "Agronomic realities", "Extensive crops", "Intensive crops" ], "skillCount" : 27, "jobCategory" : "other", "jobSubcategory" : "Sales", "dataQualityScore" : 1.0, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biological Products" }, { "id" : "6a2d6f8b74d8ee00a0be3111", "title" : "Chemical Operator", "company" : "Koppers Inc.", "industry" : "Manufacturing", "salary" : { "min" : 52000.0, "max" : 78000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Chemical Operator in Rock Hill, United States, adjusted for industry and company size." }, "location" : "Rock Hill, SC", "locations" : [ "Rock Hill, SC", "United States of America" ], "timestamp" : "2026-06-16T00:56:26.074", "fingerprint" : "662ff9b94f5ef2ba0f770900c08de38da1f492d6780cb6bdd1551385b13ef3d4", "source" : "workday", "language" : "en", "applyUrl" : "https://koppers.wd5.myworkdayjobs.com/Koppers/job/Rock-Hill-SC/Chemical-Operator_REQ03043", "externalId" : "REQ03043", "industryFunction" : { }, "locationPoint" : "38.60755,-90.37845", "structuredLocations" : [ { "city" : "Rock Hill", "state" : "South Carolina", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.9248667,-81.0250784" } ], "locationText" : "Rock Hill, South Carolina, United States", "employmentType" : "FULL_TIME", "hardSkillsList" : [ "Basic lab testing" ], "hardSkills" : [ { "name" : "Basic lab testing", "level" : "intermediate" } ], "majorSkills" : "Plant production, Operating efficiency, Regulatory compliance", "majorSkillsList" : [ "Plant production", "Operating efficiency", "Regulatory compliance" ], "coreResponsibilities" : "Maintain safety, Maintain plant production, Maintain operating efficiency, Maintain regulatory compliance, Follow safety rules, Encourage safety practices, Foster positive work environment, Maintain positive work environment, Prepare material for batch process, Charge material into batch process, Operate forklift, Load trailers, Unload trailers, Transport materials, Perform basic lab testing, Count inventory daily, Report inventory daily, Assist monthly inventory counts, Perform lock out tag out, Maintain work area clean, Maintain work area organized, Maintain work area safe, Maintain accurate records, Enter batch sheets, Enter lab data, Complete shift turnover documents, Recommend production improvements, Recommend equipment improvements, Assist in troubleshooting problems, Perform other duties", "teamCollaboration" : "Assist others", "domainKnowledge" : "Chemical plant operations", "domainList" : [ "chemical-plant-operations" ], "domainSpecificKnowledge" : [ "Chemical plant operations" ], "toolProficiency" : [ "HMIs", "Forklift" ], "communicationSkills" : "Verbal communication; Written communication", "documentationSkills" : "Batch sheets; Lab data entries; Shift turnover documents", "innovationCreativity" : "Improve production methods; Improve equipment", "problemSolvingSkills" : "Troubleshooting problems", "specialRequirements" : "Ability to climb steps, stairs, and ladders on a repetitive basis", "qualificationsBasic" : "Basic computer literacy, Mechanical aptitude, Ability to climb steps, stairs, and ladders, Ability to perform basic mathematical calculations, Ability to communicate effectively, Ability to follow instructions, Ability to work independently, Reliable transportation, Dependability, Punctuality", "qualificationsPreferred" : "Previous chemical plant experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Job Responsibilities** The Chemical Operator is responsible for maintaining safety, plant production, operating efficiency and regulatory compliance * Follows and encourages others to follow all organizational safety rules and practices. * Fosters & maintains a positive work environment. * Performs basic tasks interacting with pumps, pipes, valves, and HMIs to prepare and charge material into the manufacturing batch process. * Operates a forklift to load/unload trailers and transport materials. * Performs basic lab testing. * Counts and report inventory daily and assist monthly inventory counts. * Folows and perform lock out tag out (LOTO) for maintenance work on equipment. * Maintain work area in a clean, organized, and safe environment. * Maintain accurate records including batch sheets, lab data entries, and shift turnover documents. * Recommends methods to improve production methods and equipment. * Assists others in troubleshooting problems. * Performs other duties as assigned. **Candidate Qualifications/ Requirements** * Basic computer literacy. * Strong mechanical aptitude. * Previous chemical plant experience preferred. * Ability to climb steps, stairs, and ladders on a repetitive basis. * Basic computer literacy. * Ability to perform basic mathematical calculations necessary for position’s essential duties. * Ability to communicate effectively both verbally and in writing. * Ability to follow instructions and work independently * Reliable transportation for attendance required. * Dependability and Punctuality are key ingredients to be successful in this position. _Koppers Inc. and its subsidiaries are equal opportunity employers. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other category or characteristic protected by federal law, state, or local law._", "summaryDescription" : "Chemical Operator at Koppers Inc.. Skills: Plant production, Operating efficiency, Regulatory compliance. Maintain safety. Maintain plant production", "postedDate" : "2026-06-09T18:55:45.228", "createdAt" : "2026-06-14T18:55:45.217", "lastUpdated" : "2026-06-16T00:56:26.074", "ingestTimestamp" : "2026-06-14T18:55:45.217", "mongoId" : "6a2d6f8b74d8ee00a0be3111", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://koppers.wd5.myworkdayjobs.com/Koppers/job/Rock-Hill-SC/Chemical-Operator_REQ03043", "salaryAnnualMin" : 52000, "salaryAnnualMax" : 78000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Basic lab testing", "Plant production", "Operating efficiency", "Regulatory compliance", "Chemical plant operations", "HMIs", "Forklift" ], "skillCount" : 7, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "daysOld" : 6, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Manufacturing", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2cb20774d8ee00a09def4d", "title" : "Biological Safety Specialist", "industry" : "Legal", "location" : "Romania", "locations" : [ "Romania" ], "certifications" : [ ], "timestamp" : "2026-06-15T13:35:13.121", "fingerprint" : "1f0ae6cff6701417945c8c1f45b4ebb5ae89a97d51168d65658d2045ebe0090f", "source" : "lever", "applyUrl" : "https://jobs.lever.co/jobgether/ac0d5c9f-bcb2-4d40-bd31-437d7790e923/apply", "externalId" : "ac0d5c9f-bcb2-4d40-bd31-437d7790e923", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Romania", "continent" : "eu", "workMode" : "onsite" } ], "locationText" : "Romania", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "Mid", "technicalSkills" : "biological safety, biocompatibility, material characterization", "professionalSkills" : [ "medical device regulations and international standards related to biological safety and biocompatibility." ], "hardSkillsList" : [ "knowledge of medical device regulations", "international standards related to biological safety and biocompatibility", "assessing compliance of biocompatibility studies", "material characterization against regulatory requirements", "writing technical and regulatory documentation", "reviewing technical and regulatory documentation", "managing technical and regulatory documentation", "Microsoft Word" ], "softSkillsList" : [ "analytical thinking, critical thinking, attention to detail, scientific accuracy, communication skills, collaboration skills" ], "hardSkills" : [ { "name" : "knowledge of medical device regulations", "level" : "intermediate" }, { "name" : "international standards related to biological safety and biocompatibility", "level" : "intermediate" }, { "name" : "assessing compliance of biocompatibility studies", "level" : "intermediate" }, { "name" : "material characterization against regulatory requirements", "level" : "intermediate" }, { "name" : "writing technical and regulatory documentation", "level" : "intermediate" }, { "name" : "reviewing technical and regulatory documentation", "level" : "intermediate" }, { "name" : "managing technical and regulatory documentation", "level" : "intermediate" }, { "name" : "Microsoft Word", "level" : "intermediate" } ], "softSkills" : [ { "name" : "analytical thinking, critical thinking, attention to detail, scientific accuracy, communication skills, collaboration skills" } ], "majorSkills" : "biological safety documentation, biocompatibility assessment, medical device regulations, technical and regulatory documentation, risk assessments", "majorSkillsList" : [ "biological safety documentation, biocompatibility assessment, medical device regulations, technical and regulatory documentation, risk assessments" ], "coreResponsibilities" : "Develop, review, and maintain biological safety documentation and reports in compliance with applicable international standards and medical device regulations. Assess and audit biocompatibility and material characterization data to ensure alignment with regulatory requirements and safety expectations. Interpret complex scientific and technical information to support risk assessments and regulatory submissions for medical devices. Collaborate with cross-functional teams to ensure biological safety considerations are integrated throughout the product development lifecycle. Review and contribute to the development of complex technical and regulatory documents with a high level of accuracy and scientific rigor. Support continuous improvement of biological safety processes, methodologies, and compliance frameworks.", "teamCollaboration" : "Collaborate with cross-functional teams to ensure biological safety considerations are integrated throughout the product development lifecycle.", "toolProficiency" : [ "Microsoft Word" ], "communicationSkills" : "communication skills in multidisciplinary and regulated environments", "documentationSkills" : "biological safety documentation; technical documentation; regulatory documentation", "continuousLearning" : "Support continuous improvement of biological safety processes, methodologies, and compliance frameworks.", "problemSolvingSkills" : "risk assessments; scientific rigor", "specialRequirements" : "Fluency in proficiency in the local language (if different) is required.", "outcomesObjectives" : "Contribute to medical technologies that directly improve healthcare outcomes worldwide.", "qualificationsBasic" : "Bachelor’s degree with at least 5 years of relevant experience, or Master’s/Doctorate degree with at least 2 years of relevant experience in a scientific or related discipline.", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Accountabilities Develop, review, and maintain biological safety documentation and reports in compliance with applicable international standards and medical device regulations. Assess and audit biocompatibility and material characterization data to ensure alignment with regulatory requirements and safety expectations. Interpret complex scientific and technical information to support risk assessments and regulatory submissions for medical devices. Collaborate with cross-functional teams to ensure biological safety considerations are integrated throughout the product development lifecycle. Review and contribute to the development of complex technical and regulatory documents with a high level of accuracy and scientific rigor. Support continuous improvement of biological safety processes, methodologies, and compliance frameworks. Requirements: Bachelor’s degree with at least 5 years of relevant experience, or Master’s/Doctorate degree with at least 2 years of relevant experience in a scientific or related discipline. Strong knowledge of medical device regulations and international standards related to biological safety and biocompatibility. Experience assessing compliance of biocompatibility studies and material characterization against regulatory requirements. Proven ability to write, review, and manage complex technical and regulatory documentation. Strong analytical and critical thinking skills with attention to detail and scientific accuracy. Proficiency in Microsoft Word and other standard documentation tools. Fluency in English; proficiency in the local language (if different) is required. Strong communication and collaboration skills in multidisciplinary and regulated environments. Benefits: Opportunity to work at the forefront of medical device safety and regulatory science. Exposure to global standards and internationally recognized regulatory frameworks. Collaborative, science-driven work environment focused on innovation and patient safety. Professional development within a highly specialized and regulated industry. Chance to contribute to medical technologies that directly improve healthcare outcomes worldwide. Competitive compensation and benefits package (based on location and experience). ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Biological Safety Specialist. Skills: biological safety documentation, biocompatibility assessment, medical device regulations, technical and regulatory documentation, risk assessments. Develop, review, and maintain biological safety documentation and reports in compliance with applicable international standards and medical device regulations. Assess and audit biocompatibility and material characterization data to ensure alignment with regulatory requirements and safety expectations. Interpret c", "postedDate" : "2026-06-09T11:47:58.085", "createdAt" : "2026-06-09T11:47:58.085", "lastUpdated" : "2026-06-15T13:35:13.121", "ingestTimestamp" : "2026-06-14T21:42:09.451", "mongoId" : "6a2cb20774d8ee00a09def4d", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "hasSalary" : false, "allSkills" : [ "knowledge of medical device regulations", "international standards related to biological safety and biocompatibility", "assessing compliance of biocompatibility studies", "material characterization against regulatory requirements", "writing technical and regulatory documentation", "reviewing technical and regulatory documentation", "managing technical and regulatory documentation", "Microsoft Word", "analytical thinking, critical thinking, attention to detail, scientific accuracy, communication skills, collaboration skills", "biological safety documentation, biocompatibility assessment, medical device regulations, technical and regulatory documentation, risk assessments", "medical device regulations and international standards related to biological safety and biocompatibility." ], "skillCount" : 11, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "daysOld" : 6, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2cb20774d8ee00a09def45", "title" : "Biological Safety Specialist", "industry" : "Legal", "salary" : { "min" : 38000.0, "max" : 55000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Biological Safety Specialist in Spain, adjusted for the biotech industry and full-time employment." }, "location" : "Spain", "locations" : [ "Spain" ], "timestamp" : "2026-06-16T06:16:30.510", "fingerprint" : "c205bb1617e705518e6c42aad637ad6dc78ac6304a1c974c36ddc57e9f990413", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/jobgether/2d18f53b-7024-45a1-8d25-3712b8adfca2/apply", "externalId" : "2d18f53b-7024-45a1-8d25-3712b8adfca2", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Spain", "continent" : "eu", "workMode" : "onsite" } ], "locationText" : "Spain", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 2, "professionalSkills" : [ "Risk assessment", "Regulatory submissions" ], "hardSkillsList" : [ "Biocompatibility assessment", "Material characterization" ], "hardSkills" : [ { "name" : "Biocompatibility assessment", "level" : "intermediate" }, { "name" : "Material characterization", "level" : "intermediate" } ], "majorSkills" : "Biological safety, Regulatory compliance, Medical device innovation", "majorSkillsList" : [ "Biological safety", "Regulatory compliance", "Medical device innovation" ], "coreResponsibilities" : "Develop biological safety documentation, Review biological safety documentation, Maintain biological safety documentation, Assess biocompatibility data, Audit biocompatibility data, Assess material characterization data, Audit material characterization data, Interpret scientific information, Interpret technical information, Support risk assessments, Support regulatory submissions, Integrate safety considerations, Review technical documents, Contribute to technical documents, Review regulatory documents, Contribute to regulatory documents, Support process improvement, Support methodology improvement, Support compliance framework improvement", "teamCollaboration" : "Cross-functional teams; External stakeholders", "domainKnowledge" : "Medical device regulations; Biological safety; Biocompatibility; Material characterization", "domainList" : [ "medical-device-regulations", "biological-safety", "biocompatibility", "material-characterization" ], "domainSpecificKnowledge" : [ "Medical device regulations", "Biological safety", "Biocompatibility", "Material characterization" ], "toolProficiency" : [ "Microsoft Word" ], "documentationSkills" : "Technical documentation; Regulatory documentation", "innovationCreativity" : "Medical device innovation", "problemSolvingSkills" : "Analytical thinking; Critical thinking", "outcomesObjectives" : "Ensure product compliance; Improve healthcare outcomes", "qualificationsBasic" : "Bachelor's degree with 5 years experience, Master's/Doctorate degree with 2 years experience, Knowledge of medical device regulations, Knowledge of international standards, Experience assessing biocompatibility studies, Experience assessing material characterization, Ability to write technical documentation, Ability to review technical documentation, Ability to manage technical documentation, Analytical and critical thinking skills, Proficiency in Microsoft Word, Proficiency in standard documentation tools, Fluency in local language", "qualificationsPreferred" : "Experience with biological safety, Experience with biocompatibility, Experience with material characterization, Scientific rigor", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Description This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Biological Safety Specialist based in Spain. This role sits at the intersection of science, regulation, and medical device innovation, ensuring that products meet the highest standards of biological safety throughout their development lifecycle. You will contribute directly to the safety and compliance of medical technologies that impact patient health globally. Working within a highly specialized and regulated environment, you will evaluate scientific data, assess biocompatibility, and support the creation of critical regulatory documentation. The position involves close collaboration with multidisciplinary teams and external stakeholders to ensure alignment with international standards. You will play a key role in shaping safety assessments that influence product approval and market readiness. This is a detail-driven and impact-focused role suited for professionals passionate about science, compliance, and healthcare innovation. ## Accountabilities Develop, review, and maintain biological safety documentation and reports in compliance with applicable international standards and medical device regulations. Assess and audit biocompatibility and material characterization data to ensure alignment with regulatory requirements and safety expectations. Interpret complex scientific and technical information to support risk assessments and regulatory submissions for medical devices. Collaborate with cross-functional teams to ensure biological safety considerations are integrated throughout the product development lifecycle. Review and contribute to the development of complex technical and regulatory documents with a high level of accuracy and scientific rigor. Support continuous improvement of biological safety processes, methodologies, and compliance frameworks. Requirements: Bachelor’s degree with at least 5 years of relevant experience, or Master’s/Doctorate degree with at least 2 years of relevant experience in a scientific or related discipline. Strong knowledge of medical device regulations and international standards related to biological safety and biocompatibility. Experience assessing compliance of biocompatibility studies and material characterization against regulatory requirements. Proven ability to write, review, and manage complex technical and regulatory documentation. Strong analytical and critical thinking skills with attention to detail and scientific accuracy. Proficiency in Microsoft Word and other standard documentation tools. Fluency in English; proficiency in the local language (if different) is required. Strong communication and collaboration skills in multidisciplinary and regulated environments. Benefits: Opportunity to work at the forefront of medical device safety and regulatory science. Exposure to global standards and internationally recognized regulatory frameworks. Collaborative, science-driven work environment focused on innovation and patient safety. Professional development within a highly specialized and regulated industry. Chance to contribute to medical technologies that directly improve healthcare outcomes worldwide. Competitive compensation and benefits package (based on location and experience). ## Additional Information How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1", "summaryDescription" : "Biological Safety Specialist. Skills: Biological safety, Regulatory compliance, Medical device innovation. Develop biological safety documentation. Review biological safety documentation", "postedDate" : "2026-06-09T11:46:24.758", "createdAt" : "2026-06-09T11:46:24.758", "lastUpdated" : "2026-06-16T06:16:30.510", "ingestTimestamp" : "2026-06-14T21:05:38.700", "mongoId" : "6a2cb20774d8ee00a09def45", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ "Biocompatibility assessment", "Material characterization", "Biological safety", "Regulatory compliance", "Medical device innovation", "Risk assessment", "Regulatory submissions", "Medical device regulations", "Biocompatibility", "Microsoft Word" ], "skillCount" : 10, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "daysOld" : 6, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c617474d8ee00a08f49bc", "title" : "Materials Chemistry/Chemical Engineering Intern (FALL 2026)", "salary" : { "min" : 41000.0, "max" : 55000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level intern in the technology industry in Waltham, United States, adjusted for city tier and seniority." }, "location" : "Waltham, MA", "locations" : [ "Waltham, MA" ], "timestamp" : "2026-06-15T05:01:24.966", "fingerprint" : "f05e474c0802048304f603c55a6da6d8dae98e5109ac456ff5f1c13c4a91f6e8", "source" : "jazzhr", "language" : "en", "externalId" : "PIjWPOj8G0", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Waltham", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.3762385,-71.2355644" } ], "locationText" : "Waltham, Massachusetts, United States", "employmentType" : "INTERNSHIP", "summaryDescription" : "Materials Chemistry/Chemical Engineering Intern (FALL 2026)", "createdAt" : "2026-06-14T05:23:09.175", "lastUpdated" : "2026-06-15T05:01:24.966", "ingestTimestamp" : "2026-06-14T05:23:09.175", "mongoId" : "6a2c617474d8ee00a08f49bc", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 41000, "salaryAnnualMax" : 55000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Entry", "dataQualityScore" : 0.44444445, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.85 }, { "id" : "6a2d90fa74d8ee00a0c380f6", "title" : "Senior Process/Chemical Engineer", "company" : "AtkinsRéalis US Nuclear", "industry" : "Government", "salary" : { "min" : 90000.0, "max" : 150000.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "US.TN.Oak Ridge.545 Oak Ridge Turnpike", "locations" : [ "US.TN.Oak Ridge.545 Oak Ridge Turnpike", "United States of America" ], "certifications" : [ "Professional Engineering (PE) License" ], "timestamp" : "2026-06-16T03:10:12.886", "fingerprint" : "e5169f2de20c7fb52148a40550273568ec768968044e833bea90ee7d363ae238", "source" : "workday", "language" : "en", "applyUrl" : "https://slihrms.wd3.myworkdayjobs.com/Careers/job/USTNOak-Ridge545-Oak-Ridge-Turnpike/Senior-Process-Chemical-Engineer---Remote_R-156994-2", "externalId" : "R-156994", "industryFunction" : { }, "locationPoint" : "32.65735,-96.2622", "structuredLocations" : [ { "country" : "Bulgaria", "continent" : "eu", "workMode" : "remote" } ], "locationText" : "Bulgaria", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Process simulation software", "professionalSkills" : [ "System architecture", "Flow diagrams", "Piping/instrumentation diagrams", "Mechanical components", "Valves", "Vessels", "Mass balance", "Energy balance", "Flow balance", "Pipe sizing", "Equipment sizing", "Process equipment specifications", "Design deliverables", "Change control" ], "hardSkillsList" : [ "Chemical safety", "Criticality controls", "Radiation shielding", "Defense-in-depth principles" ], "hardSkills" : [ { "name" : "Chemical safety", "level" : "intermediate" }, { "name" : "Criticality controls", "level" : "intermediate" }, { "name" : "Radiation shielding", "level" : "intermediate" }, { "name" : "Defense-in-depth principles", "level" : "intermediate" } ], "majorSkills" : "Process engineering, Nuclear facilities, P&IDs", "majorSkillsList" : [ "Process engineering", "Nuclear facilities", "P&IDs" ], "coreResponsibilities" : "Develop system architecture, Conceptualize flow diagrams, Conceptualize piping/instrumentation diagrams, Perform rigorous evaluations, Ensure systems maintain chemical safety, Ensure systems maintain criticality controls, Ensure systems maintain radiation shielding, Ensure systems maintain defense-in-depth principles, Select mechanical components, Test mechanical components, Specify mechanical components, Evaluate test data, Improve efficiency of existing nuclear facilities, Develop key design deliverables, Prepare calculations, Check calculations, Approve calculations, Prepare engineering documents, Ensure design deliverables are of high standard, Ensure design deliverables are compliant with standards, Ensure design consultants deploy qualified personnel, Ensure sub-contractors deploy qualified personnel, Produce technically accurate documentation, Develop resolutions to complex problems, Develop resolutions to technical issues, Implement necessary change control, Work independently, Act as a resource for colleagues, Perform other duties as assigned", "teamCollaboration" : "Design consultants; Sub-contractors", "domainKnowledge" : "Nuclear sector; Nuclear facilities; Nuclear power generation; Fuel cycle assets; Small Modular Reactor; Nuclear fuel cycle facility; Commercial nuclear facilities; DOE regulations; NRC regulations; Nuclear quality assurance", "domainList" : [ "nuclear-sector", "nuclear-facilities", "nuclear-power-generation", "fuel-cycle-assets", "small-modular-reactor", "nuclear-fuel-cycle-facility", "commercial-nuclear-facilities", "doe-regulations", "nrc-regulations", "nuclear-quality-assurance" ], "domainSpecificKnowledge" : [ "Nuclear sector", "Nuclear facilities", "Nuclear power generation", "Fuel cycle assets", "Small Modular Reactor", "Nuclear fuel cycle facility", "Commercial nuclear facilities", "DOE regulations", "NRC regulations", "Nuclear quality assurance" ], "communicationSkills" : "Communication skills", "documentationSkills" : "Process drawings; Process Flow Diagrams; Process & Instrumentation Diagrams; Engineering Flow Diagrams; Specifications for process equipment; Grammatically correct documentation; Correctly formatted documentation; Professionally presented documentation", "problemSolvingSkills" : "Complex problem resolution; Technical issue resolution", "specialRequirements" : "U. S. citizen", "qualificationsBasic" : "Bachelor's degree in Chemical Engineering, Minimum of five (5) years post-baccalaureate experience, Previous experience providing engineering support to nuclear facility design, construction or operations, Knowledge of key NRC regulations, Knowledge of design codes and standards for commercial nuclear facilities, Knowledge in the use of related design software codes, Knowledge in process simulation software, Must be a U. S. citizen", "qualificationsPreferred" : "Professional Engineering (PE) License preferred, Design of Commercial and Department of Energy nuclear reactor projects, Design of Commercial and Department of Energy nuclear fuel cycle facilities, Nuclear Steam Supply System (NSSS) Original Equipment Manufacturer (OEM) experience", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "### **Job Description** ## **Overview** We are seeking **a Senior Process/Chemical Engineer – Energy – Remote. This remote position is based out of our Oak Ridge, TN office.** ## ## **Your role** * AtkinsRéalis US Nuclear is the subsidiary of AtkinsRéalis focused on serving government and commercial clients within the Nuclear sector in the United States. We are focused on being recognized as a premier nuclear solutions company in the United States, delivering engineering, operations, and project management services. * Serves both legacy and new build nuclear clients who are designing, building, upgrading, operating and maintaining nuclear power generation and fuel cycle assets. * We are a growing business, building on the foundation of our US government fuel cycle business, our international position as an Original Equipment Manufactor (OEM) and nuclear reactor technology provider, and our world-wide nuclear new build and legacy nuclear fleet maintenance experience. * Executes Small Modular Reactor and nuclear fuel cycle facility projects. * Develops and conceptualizes system architecture, flow diagrams, and piping/instrumentation diagrams (P&IDs) for nuclear facilities, auxiliary systems, or fuel cycle models. * Performs rigorous evaluations to ensure that systems, structures and components maintain chemical safety, criticality controls, radiation shielding, and defense-in-depth principles under normal and off-normal conditions, including accident scenarios. * Ensures that all engineering designs align with local, state, and federal standards, including DOE or NRC regulations. You select, test, and specify mechanical components, valves, and vessels to ensure they withstand highly regulated and hazardous environments. * Evaluates test or validation data to improve the efficiency of existing nuclear facilities. * Develops key design deliverables such as Process drawings, Process Flow Diagrams and Process & Instrumentation Diagrams/Engineering Flow Diagrams. * Prepares, checks and/or approves calculations including mass, energy and flow balances, and pipe and equipment sizing. * Prepares engineering documents such as specifications for process equipment. * Ensures that design deliverables are of a high standard and compliant with relevant standards, regulations and customer specific standards, including nuclear quality assurance standards. * Ensures that design consultants and sub-contractors deploy suitably qualified and experienced personnel. * Produces documentation that is technically accurate, grammatically correct, correctly formatted and professionally presented. * Develops resolutions to complex problems or technical issues and ensure necessary change control is implemented. * Works independently receiving only minimal guidance. * May act as a resource for other colleagues with less experience. * Performs other duties as assigned. ## **About you** * Bachelor's degree in Chemical Engineering or related field. * Minimum of five (5) years post-baccalaureate experience. * Previous experience providing engineering support to nuclear facility design, construction or operations. * Strong communication skills in a challenging, multi-tiered environment. * Strong organizational skills. * Knowledge of key NRC regulations, design codes and standards for commercial nuclear facilities required. * Knowledge in the use of related design software codes, including process simulation software. * Professional Engineering (PE) License preferred. * Design of Commercial and Department of Energy nuclear reactor projects. * Design of Commercial and Department of Energy nuclear fuel cycle facilities. * Nuclear Steam Supply System (NSSS) Original Equipment Manufacturer (OEM) experience. * Must be a U.S. citizen in order to be considered. ## ## ## **Rewards & benefits** At AtkinsRéalis, our values—Safety, Integrity, Collaboration, Innovation, and Excellence—are more than just words. They are the foundation of who we are and how we work. These principles shape our culture, guide our decisions, and inspire us to create an environment where every team member feels empowered to grow, succeed, and make a meaningful impact. Depending on your employment status, AtkinsRéalis benefits may include medical, dental, vision, company-paid life and short- and long-term disability benefits, employer-matched 401(k) with 100% vesting, employee stock purchase plan, Paid Time Off, leaves of absences options, flexible work options, recognition and employee satisfaction programs, employee assistance program, and voluntary benefits. You can review our comprehensive benefits page [here](https://careers.atkinsrealis.com/rewards-benefits-us). ## **About AtkinsRéalis** We're [AtkinsRéalis](https://careers.atkinsrealis.com/), a world-class engineering services and nuclear organization. We connect people, data and technology to transform the world's infrastructure and energy systems. Together, with our industry partners and clients, and our global team of consultants, designers, engineers and project managers, we can change the world. We're committed to leading our clients across our various end markets to engineer a better future for our planet and its people. [Find out more.](https://careers.atkinsrealis.com/) ## **Additional information** **Expected compensation range is between $90,000-$150,000 annually depending on skills, experience, and geographical location.** **Are you ready to expand your career with us? Apply today and help us shape something extraordinary.** **AtkinsRéalis is an equal opportunity, Drug-Free employer EOE/Veteran/Disability** Please review AtkinsRéalis’ Equal Opportunity Statement [here](https://careers.atkinsrealis.com/equal-opportunities-statement). **AtkinsRéalis cares about your privacy** and is committed to protecting your privacy. Please consult our [Privacy Notice](https://careers.atkinsrealis.com/privacy-statement) our Careers site to know more about how we collect, use and transfer your Personal Data. By submitting your personal information to AtkinsRéalis, you confirm that you have read and accept our Privacy Notice. **Note to staffing and direct hire agencies:** In the event a recruiter or agency who is not on our preferred supplier list submits a resume/candidate to anyone in the company, AtkinsRéalis family of companies, we explicitly reserve the right to recruit and hire the candidate(s) at our discretion and without any financial obligation to the recruiter or agency. #LI-Remote ### **Worker Type** Employee ### **Job Type** Regular _At_ _AtkinsRéalis_ _, we seek to hire individuals with diverse characteristics, backgrounds and perspectives. We strongly believe that world-class talent makes no distinctions based on gender, ethnic or national origin, sexual identity and orientation, age, religion or disability, but enriches itself through these differences._", "summaryDescription" : "Senior Process/Chemical Engineer at AtkinsRéalis US Nuclear. Skills: Process engineering, Nuclear facilities, P&IDs. Develop system architecture. Conceptualize flow diagrams", "postedDate" : "2026-06-10T19:01:30.185", "createdAt" : "2026-06-14T19:01:30.111", "lastUpdated" : "2026-06-16T03:10:12.886", "ingestTimestamp" : "2026-06-14T19:01:30.111", "mongoId" : "6a2d90fa74d8ee00a0c380f6", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://slihrms.wd3.myworkdayjobs.com/Careers/job/USTNOak-Ridge545-Oak-Ridge-Turnpike/Senior-Process-Chemical-Engineer---Remote_R-156994-2", "salaryAnnualMin" : 90000, "salaryAnnualMax" : 150000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Chemical safety", "Criticality controls", "Radiation shielding", "Defense-in-depth principles", "Process engineering", "Nuclear facilities", "P&IDs", "System architecture", "Flow diagrams", "Piping/instrumentation diagrams", "Mechanical components", "Valves", "Vessels", "Mass balance", "Energy balance", "Flow balance", "Pipe sizing", "Equipment sizing", "Process equipment specifications", "Design deliverables", "Change control", "Nuclear sector", "Nuclear power generation", "Fuel cycle assets", "Small Modular Reactor", "Nuclear fuel cycle facility", "Commercial nuclear facilities", "DOE regulations", "NRC regulations", "Nuclear quality assurance", "Professional Engineering (PE) License" ], "skillCount" : 31, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "senior", "dataQualityScore" : 1.0, "daysOld" : 5, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Nuclear", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2af57474d8ee00a073a3d0", "title" : "Chemical Biologist", "company" : "Guidehouse", "salary" : { "min" : 98000.0, "max" : 163000.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "US - MD, Bethesda", "locations" : [ "US - MD, Bethesda", "United States of America" ], "timestamp" : "2026-06-14T19:10:37.385", "fingerprint" : "c8a54d9a1392bf193d55e2d5f427b898cc6c005a580e3f41a3c93150c7c8fa38", "source" : "workday", "language" : "en", "applyUrl" : "https://guidehouse.wd1.myworkdayjobs.com/External/job/US---MD-Bethesda/Chemical-Biologist_40260", "externalId" : "40260", "locationPoint" : "53.1815,-4.05828", "structuredLocations" : [ { "city" : "Bethesda", "state" : "Maryland", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.9812726,-77.1233587" }, { "city" : "Rockville", "state" : "Maryland", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "39.0817985,-77.1516844" }, { "city" : "Potomac", "state" : "Maryland", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "39.0180508,-77.1956331" }, { "city" : "Herndon", "state" : "Virginia", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.9695316,-77.3859479" }, { "city" : "Reston", "state" : "Virginia", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.9532820,-77.3464516" }, { "city" : "Sterling", "state" : "Virginia", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "39.0036850,-77.4083096" }, { "city" : "McLean", "state" : "Virginia", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.9366852,-77.1858430" } ], "locationText" : "Bethesda, Maryland, United States; Rockville, Maryland, United States; Potomac, Maryland, United States; Herndon, Virginia, United States; Reston, Virginia, United States; Sterling, Virginia, United States; McLean, Virginia, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "PhD", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "Mid", "technicalSkills" : "Peptide synthesis, Small molecule synthesis, mRNA expression, Peptide conjugation, Antibody fragment preparation", "professionalSkills" : [ "Chemical biology", "Drug discovery", "Diagnostic imaging", "Target validation" ], "hardSkillsList" : [ "Cyclic peptide generation", "Cyclic peptide screening", "Cyclic peptide synthesis", "Cyclic peptide optimization", "Compound screening", "Compound synthesis", "Compound optimization", "Analytical instrumentation" ], "hardSkills" : [ { "name" : "Cyclic peptide generation", "level" : "intermediate" }, { "name" : "Cyclic peptide screening", "level" : "intermediate" }, { "name" : "Cyclic peptide synthesis", "level" : "intermediate" }, { "name" : "Cyclic peptide optimization", "level" : "intermediate" }, { "name" : "Compound screening", "level" : "intermediate" }, { "name" : "Compound synthesis", "level" : "intermediate" }, { "name" : "Compound optimization", "level" : "intermediate" }, { "name" : "Analytical instrumentation", "level" : "intermediate" } ], "majorSkills" : "Peptide synthesis, Small molecule synthesis, Chemical biology, Drug discovery", "majorSkillsList" : [ "Peptide synthesis", "Small molecule synthesis", "Chemical biology", "Drug discovery" ], "coreResponsibilities" : "Synthesize small cyclic peptides, Optimize small cyclic peptides, Design small molecules, Develop small molecules, Develop mRNA-based peptide expression systems, Perform peptide conjugation, Prepare antibody fragments, Conjugate antibody fragments, Conduct compound screening, Conduct compound synthesis, Conduct compound optimization, Utilize analytical instrumentation, Characterize compounds, Ensure quality, Document experimental results, Communicate experimental results", "teamCollaboration" : "Multidisciplinary teams; Service-oriented research", "domainKnowledge" : "Diagnostic imaging; Drug discovery; MRI; Optical imaging; PET imaging; Nanoparticles", "domainList" : [ "diagnostic-imaging", "drug-discovery", "mri", "optical-imaging", "pet-imaging", "nanoparticles" ], "domainSpecificKnowledge" : [ "Diagnostic imaging", "Drug discovery", "MRI", "Optical imaging", "PET imaging", "Nanoparticles" ], "communicationSkills" : "Reports; Presentations", "documentationSkills" : "Experimental results", "continuousLearning" : "Personal development; Certifications; Learning opportunities", "specialRequirements" : "Ability to Obtain Public Trust", "qualificationsBasic" : "PhD in Chemistry or related field, 2 years laboratory research experience, Master's degree in Chemistry or related field, 4 years laboratory research experience, Obtain Public Trust clearance", "qualificationsPreferred" : "Active public trust clearance", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**_Job Family_ :** Scientist ** _Travel Required_ :** None ** _Clearance Required_ :** Ability to Obtain Public Trust ** _What You Will Do_ :** We are currently searching for a Chemical Biologist to provide support services to satisfy the overall operational objectives of the National Heart, Lung, and Blood Institute (NHLBI). This is a full-time, on-site opportunity in Bethesda, MD. * Synthesize and optimize small cyclic peptides for diagnostic imaging and early-stage drug discovery applications. * Design and develop small molecules as chemical tools to support biological research, including target validation and imaging (MRI, optical, PET). * Develop and implement mRNA-based peptide expression systems for cyclic peptide production. * Perform peptide conjugation, including linking to fluorescent dyes, chelators, or imaging agents. * Prepare and characterize antibody fragments (e.g., nanobodies, Fab2) and conjugate them for imaging applications. * Conduct compound screening, synthesis, and optimization workflows. * Utilize modern analytical instrumentation to characterize compounds and ensure quality. * Collaborate closely with multidisciplinary teams in a service-oriented research environment. * Document and communicate experimental results effectively through reports and presentations. **_What You Will Need_ :** * Ph.D. in Chemistry, Biochemistry, or related field with a minimum of TWO (2) years of laboratory research experience OR Master's degree in Chemistry, Biochemistry, or related field with a minimum of FOUR (4) years of laboratory research in lieu of Ph.D. * Demonstrated expertise in cyclic peptide generation, screening, synthesis, and optimization. * Strong background in synthetic chemistry, including small molecule and peptide synthesis. * Knowledge of chemical biology approaches for drug discovery or imaging applications. * Experience with or knowledge of fluorescent dyes, chelators for radioactive metals, MRI agents and nanoparticles. * Must be able to obtain and maintain a Federal or DoD “public trust”; candidates must receive approved adjudication prior to onboarding with Guidehouse. Candidates with an active public trust or suitability are preferred. **_What Would Be Nice To Have_ :** * Ability to design and execute complex experiments independently. * Excellent communication skills. * Proven ability to work effectively in a collaborative, team-based environment. The annual salary range for this position is $98,000.00-$163,000.00. Compensation decisions depend on a wide range of factors, including but not limited to skill sets, experience and training, security clearances, licensure and certifications, and other business and organizational needs. _**What We Offer:**_ Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace. Benefits include: * Medical, Rx, Dental & Vision Insurance * Personal and Family Sick Time & Company Paid Holidays * Parental Leave * 401(k) Retirement Plan * Group Term Life and Travel Assistance * Voluntary Life and AD&D Insurance * Health Savings Account, Health Care & Dependent Care Flexible Spending Accounts * Transit and Parking Commuter Benefits * Short-Term & Long-Term Disability * Tuition Reimbursement, Personal Development, Certifications & Learning Opportunities * Employee Referral Program * Corporate Sponsored Events & Community Outreach * Care.com annual membership * Employee Assistance Program * Supplemental Benefits via Corestream (Critical Care, Hospital Indemnity, Accident Insurance, Legal Assistance and ID theft protection, etc.) * Position may be eligible for a discretionary variable incentive bonus _**About Guidehouse**_ Guidehouse is an Equal Opportunity Employer–Protected Veterans, Individuals with Disabilities or any other basis protected by law, ordinance, or regulation. Guidehouse will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of applicable law or ordinance including the Fair Chance Ordinance of Los Angeles and San Francisco. If you have visited our website for information about employment opportunities, or to apply for a position, and you require an accommodation, please contact Guidehouse Recruiting at 1-571-633-1711 or via email at [RecruitingAccommodation@guidehouse.com](mailto:RecruitingAccommodation@guidehouse.com). All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodation. All communication regarding recruitment for a Guidehouse position will be sent from Guidehouse email domains including @guidehouse.com or [guidehouse@myworkday.com](mailto:guidehouse@myworkday.com). Correspondence received by an applicant from any other domain should be considered unauthorized and will not be honored by Guidehouse. Note that Guidehouse will never charge a fee or require a money transfer at any stage of the recruitment process and does not collect fees from educational institutions for participation in a recruitment event. Never provide your banking information to a third party purporting to need that information to proceed in the hiring process. If any person or organization demands money related to a job opportunity with Guidehouse, please report the matter to Guidehouse’s Ethics Hotline. If you want to check the validity of correspondence you have received, please contact [recruiting@guidehouse.com](mailto:recruiting@guidehouse.com). Guidehouse is not responsible for losses incurred (monetary or otherwise) from an applicant’s dealings with unauthorized third parties. _Guidehouse does not accept unsolicited resumes through or from search firms or staffing agencies. All unsolicited resumes will be considered the property of Guidehouse and Guidehouse will not be obligated to pay a placement fee._", "summaryDescription" : "Chemical Biologist at Guidehouse. Skills: Peptide synthesis, Small molecule synthesis, Chemical biology, Drug discovery. Synthesize small cyclic peptides. Optimize small cyclic peptides", "postedDate" : "2026-06-09T05:40:51.689", "createdAt" : "2026-06-12T05:40:51.486", "lastUpdated" : "2026-06-14T19:10:37.385", "ingestTimestamp" : "2026-06-12T05:40:51.486", "mongoId" : "6a2af57474d8ee00a073a3d0", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://guidehouse.wd1.myworkdayjobs.com/External/job/US---MD-Bethesda/Chemical-Biologist_40260", "salaryAnnualMin" : 98000, "salaryAnnualMax" : 163000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Cyclic peptide generation", "Cyclic peptide screening", "Cyclic peptide synthesis", "Cyclic peptide optimization", "Compound screening", "Compound synthesis", "Compound optimization", "Analytical instrumentation", "Peptide synthesis", "Small molecule synthesis", "Chemical biology", "Drug discovery", "Diagnostic imaging", "Target validation", "MRI", "Optical imaging", "PET imaging", "Nanoparticles" ], "skillCount" : 18, "jobCategory" : "other", "seniorityLevel" : "mid", "dataQualityScore" : 1.0, "daysOld" : 5, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2a748374d8ee00a06544a1", "title" : "Chemical Research, Development & Engineering Interest", "company" : "AIRCO", "industry" : "Technology", "location" : "New Britain, Pennsylvania, United States", "locations" : [ "New Britain", "Pennsylvania", "United States" ], "timestamp" : "2026-06-14T21:44:11.117", "fingerprint" : "453c01d4fd26571c32033f8edae66c385098f3cf1671ea05d519c8a291349b35", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/aircompany/jobs/4703884005", "externalId" : "4703884005", "industryFunction" : { }, "structuredLocations" : [ { "city" : "new britain", "state" : "connecticut", "country" : "united states", "continent" : "north america", "source" : "locations-index", "geo" : "41.66121,-72.77954" } ], "locationText" : "New Britain, Pennsylvania, United States", "domainKnowledge" : "Carbon conversion technology; Synthetic fuels; Sustainable aviation fuel", "domainList" : [ "carbon-conversion-technology", "synthetic-fuels", "sustainable-aviation-fuel" ], "domainSpecificKnowledge" : [ "Carbon conversion technology", "Synthetic fuels", "Sustainable aviation fuel" ], "specialRequirements" : "Government authorization required, Security clearance", "qualificationsBasic" : "Ability to obtain government authorization", "rawDescription" : "About AIRCO AIRCO is a world leader in carbon conversion technology, paving the way to global energy security by transforming CO₂ into a valuable resource. Its proprietary AIRMADE™ Technology is an adaptable platform that allows any industry to efficiently produce high-demand, fully-formulated synthetic fuels from waste CO₂ and hydrogen. The company has commercial partnerships with airlines including JetBlue and Virgin Atlantic, amongst others, and has been awarded multiple government contracts, including with NASA and the United States Department of Defense's Defense Innovation Unit. The company has received industry recognition through awards such as Time Best Inventions, Inc. Best in Business, Fast Company World Changing Ideas, and the XPrize for Carbon Removal. AIRCO’s many accolades include winning the prestigious Green Chemistry Challenge Award from the Environmental Protection Agency in October 2023, an award given to organizations that reinvent processes to reduce the generation of hazardous substances and byproducts. AIRCO was also declared a winner for the World Economic Forum UpLink Sustainable Aviation Challenge, which accelerates the development of promising technology pathways that enable widespread uptake of SAF. Overview Have an interest in sustainability, technology and science? Introduce yourself - we are growing and growing fast! We may not have a role posted but we'd love to meet you and keep in mind for future opportunities. At AIRCO we value employees for their unique perspectives. We are an inclusive affirmative action Equal Employment Opportunity employer. We consider applicants without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, pregnancy-related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, present or past history of intellectual, learning, mental, or physical disability (including but not limited to blindness) unless AIRCO determines that such disability prevents performance of the work involved, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances. At AIRCO we value employees for their unique perspectives. We are an inclusive affirmative action Equal Employment Opportunity employer. We consider applicants without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, pregnancy-related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, present or past history of intellectual, learning, mental, or physical disability (including but not limited to blindness) unless AIRCO determines that such disability prevents performance of the work involved, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances. Don’t meet every single requirement? Studies have shown that women, marginalized genders and people of color are less likely to apply to jobs unless they meet every single qualification. At AIRCO we are dedicated to building a diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t align perfectly with every qualification in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles This position requires access to technology, software and other information that is subject to governmental access control restrictions, due to export controls, security classification and/or designation as Controlled Unclassified Information. Employment in this position is conditioned on the candidate’s ability to obtain and maintain appropriate government authorization to access technology or information, to the extent required, including without limitation a security clearance, export license, or other documentation required to establish authorization to receive access to such items technology or information. We may delay commencement of employment, rescind an offer of employment, terminate employment, and/or modify job responsibilities, compensation, benefits, and/or access to Company facilities and information systems, as we deem appropriate, in order to ensure compliance with applicable government access control restrictions. I consent to transfer my data to Air Company in the U. S. and to its use in accordance with the Air Company Privacy Policy, and I opt in to receiving information from Air Company. Air Company does not sell or share personal information to third parties within the meanings given under applicable laws.", "summaryDescription" : "Chemical Research, Development & Engineering Interest at AIRCO", "postedDate" : "2026-06-11T19:58:43.658", "createdAt" : "2026-06-11T19:58:43.658", "lastUpdated" : "2026-06-14T21:44:11.117", "ingestTimestamp" : "2026-06-11T19:58:43.658", "mongoId" : "6a2a748374d8ee00a06544a1", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "hasSalary" : false, "allSkills" : [ "Carbon conversion technology", "Synthetic fuels", "Sustainable aviation fuel" ], "skillCount" : 3, "jobCategory" : "other", "jobSubcategory" : "future-opportunities", "dataQualityScore" : 0.6666667, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology" }, { "id" : "6a2c7c6274d8ee00a094d4dc", "title" : "Performance Engineer", "company" : "Madison Energy Infrastructure", "industry" : "Climate Tech", "salary" : { "min" : 50000.0, "max" : 75000.0, "currency" : "PHP", "frequency" : "yearly", "is_estimated" : false }, "location" : "Philippines", "locations" : [ "Philippines" ], "timestamp" : "2026-06-15T06:51:11.467", "fingerprint" : "fc57d28023d955c3c22980e01821f9d7cc585cd76c7f149d79afccac443a331f", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/madisonenergyinfrastructure/jobs/4254897009", "externalId" : "4254897009", "industryFunction" : { }, "structuredLocations" : [ { "country" : "Philippines", "continent" : "as", "workMode" : "remote" } ], "locationText" : "Philippines", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Solar, BESS", "professionalSkills" : [ "Data analysis", "Issue summarization", "Email communication" ], "hardSkillsList" : [ "Performance analysis" ], "softSkillsList" : [ "Critical thinking", "Detail-driven" ], "hardSkills" : [ { "name" : "Performance analysis", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Critical thinking" }, { "name" : "Detail-driven" } ], "majorSkills" : "Performance Engineering, Data Analysis", "majorSkillsList" : [ "Performance Engineering", "Data Analysis" ], "coreResponsibilities" : "Analyze portfolio performance, Manage portfolio performance, Write issue summaries, Write email communications", "teamCollaboration" : "Senior Manager of Analytics", "domainKnowledge" : "Solar assets; BESS assets", "domainList" : [ "solar-assets", "bess-assets" ], "domainSpecificKnowledge" : [ "Solar assets", "BESS assets" ], "toolProficiency" : [ "Zoom", "Slack", "Outlook", "Teams", "Dropbox", "Adobe", "Google Suite", "Multiplier" ], "communicationSkills" : "Issue summaries; Email communications", "problemSolvingSkills" : "Identify what's wrong; Proactive problem solving", "specialRequirements" : "Work U. S. Eastern hours, Occasional weekends, 50-hour workweek", "qualificationsBasic" : "5+ years experience, Personal computer (2022 or newer), Intel i5/Ryzen 5 or better, 8GB RAM minimum, 256GB SSD, Hardwired primary internet connection, Cellular backup internet, External monitor and headset", "qualificationsPreferred" : "Experience with Zoom, Experience with Slack, Experience with Outlook, Experience with Teams, Experience with Dropbox, Experience with Adobe, Experience with Google Suite", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "About You We are seeking an experienced, data-driven Performance Engineer to selectively analyze and manage the performance of our growing portfolio of over 600 solar and BESS assets across the United States. You will report directly to the Senior Manager of Analytics capable of writing clear, professional issue summaries and email communications. Demonstrated critical thinking: ability to look at a dataset and identify what’s wrong before being told. Enjoys structured , detail-driven work with consistent daily patterns—perfect for someone who enjoys clear routines and predictable execution. Comfortable operating independently with minimal instruction. Organized, detail-obsessed, and proactive about solving problems before they grow. Willingness to work U. S. Eastern hours, including occasional weekends. Technical Setup Requirements Because this is a fully remote role, we require the following: Personal computer (2022 or newer) with minimum specs: Intel i5/Ryzen 5 or better, 8GB RAM minimum, 256GB SSD Hardwired primary internet connection + cellular backup (minimum +10 Mbps, <20 ms ping). External monitor and headset Familiarity with Zoom, Slack, Outlook, Teams, Dropbox, Adobe, and Google Suite Compensation & Perks Base pay: 50,000–75,000 PHP/month after taxes and fees Stipends: USD $60/month healthcare stipend + USD $40/month internet stipend (tax deductible) US holiday calendar 50-hour workweek: Monday–Friday 8am–6pm ET with 1-hour lunch Weekends as needed (<25% of weekends, around 2-3 hours per day) Employment Logistics EOR Arrangement – Employment is facilitated through Multiplier.com, an employer of record (EOR) platform that ensures compliance with local employment laws and regulations in the Philippines Payroll – Paychecks are issued by Multiplier after withholding local taxes, paid semi-monthly 13th Month Pay – Handled by Multiplier as required by local law Currency Conversion – Madison covers the cost of currency conversion Time Tracking – You will use Multiplier's built-in timesheet portal How We Work At Madison Energy Infrastructure, we believe in the power of clean energy infrastructure to drive real impact—for our customers, our partners, and the communities we serve. We’ve quickly emerged as a preeminent developer, investor, and operator of distributed generation, helping organizations across sectors meet their energy goals with certainty, speed, and trust. Our robust portfolio consists of over half a gigawatt of clean energy infrastructure projects across more than 25 states. We’re building a team that thrives on ownership and ambition. As we expand into direct, end-to-end services for Fortune 500 companies, public entities, and nonprofits alike, we rely on collaborative thinkers who bring structure to complexity, energy to execution, and curiosity to every challenge. Our environment is fast-paced and outcome-oriented—but grounded in the belief that how we work together matters as much as what we deliver. If you’re excited to shape the future of clean energy and be part of a high-performance, high-integrity team, we’d love to meet you. Madison Energy Infrastructure is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.", "summaryDescription" : "Performance Engineer at Madison Energy Infrastructure. Skills: Performance Engineering, Data Analysis. Analyze portfolio performance. Manage portfolio performance", "postedDate" : "2026-06-14T08:19:20.072", "createdAt" : "2026-06-14T08:19:20.072", "lastUpdated" : "2026-06-15T06:51:11.467", "ingestTimestamp" : "2026-06-14T08:19:20.072", "mongoId" : "6a2c7c6274d8ee00a094d4dc", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "50k-75k", "hasSalary" : false, "allSkills" : [ "Performance analysis", "Critical thinking", "Detail-driven", "Performance Engineering", "Data Analysis", "Data analysis", "Issue summarization", "Email communication", "Solar assets", "BESS assets", "Zoom", "Slack", "Outlook", "Teams", "Dropbox", "Adobe", "Google Suite", "Multiplier" ], "skillCount" : 18, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Climate Tech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ebf7d74d8ee00a0e9ab8a", "title" : "Clinical Laboratory Technican - Microbiology", "company" : "Labcorp", "salary" : { "min" : 5000.0, "max" : 5000.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "United States of America", "locations" : [ "United States of America" ], "timestamp" : "2026-06-16T03:23:55.691", "fingerprint" : "79ac3bcbda815d40b96dd9911815a4303a0ae412ad0a5b4ca104743f97c1f90a", "source" : "workday", "language" : "en", "applyUrl" : "https://labcorp.wd1.myworkdayjobs.com/External/job/Birmingham-AL/Clinical-Laboratory-Technican---Microbiology_2620516", "externalId" : "2620516", "industryFunction" : { }, "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "city" : "Birmingham", "state" : "Alabama", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "33.5206824,-86.8024326" } ], "locationText" : "Birmingham, Alabama, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Associate's", "remoteFriendly" : false, "rawDescription" : "**LabCorp is seeking a Clinical Lab Professional to join our team Micro Team at UAB St. Vincent’s St. East in Birmingham, AL.** **$5,000 Sign On Bonus (External Candidates Only)** **Work Schedule:** 4 x 10 Hour Shifts, Monday – Friday 6:00 AM – 430 PM, Rotating Weekends and Holidays **Job Responsibilities:** * Determine the acceptability of specimens for testing according to established criteria * Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures * Monitor, operate and troubleshoot instrumentation to ensure proper functionality * Demonstrate the ability to make technical decisions regarding testing and problem solving. * Prepare, test and evaluate new reagents or controls * Report accurate and timely test results in order to deliver quality patient care * Perform and document preventive maintenance and quality control procedures * Identify and replenish testing bench supplies as necessary * Assist with processing of specimens when needed * Maintain a safe work environment and wear appropriate personal protective equipment **Minimum Qualifications:** * Associate’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology **Preferred Qualifications:** * 2 years or more of clinical laboratory testing experience * ASCP or AMT certification **Additional Job Standards:** * In lieu of education requirements listed above, non-traditional degrees with applicable science credits that meet CLIA standards may meet education requirement * Familiarity with laboratory information systems * Ability to work independently and within a team environment * Proficient with computers * High level of attention detail along with strong communication and organizational skills * Able to pass a standardized color blindness test * Flexibility to work overtime or other shifts depending on business needs At Labcorp we have a passion in helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career step!**This role works in a high volume, production based environment performing a vital component of clinical lab science.** **Benefits:** Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please [click here](https://careers.labcorp.com/global/en/us-rewards-and-wellness). _**If you 're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!**_ **Labcorp is proud to be an Equal Opportunity Employer:** Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. **We encourage all to apply** If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our [accessibility site](https://careers.labcorp.com/global/en/accessibility) or contact us at [Labcorp Accessibility.](mailto:Disability_apply@LabCorp.com) For more information about how we collect and store your personal data, please see our [Privacy Statement](https://www.labcorp.com/about/web-privacy-policy).", "summaryDescription" : "Clinical Laboratory Technican - Microbiology at Labcorp", "postedDate" : "2026-06-12T21:08:26.492", "createdAt" : "2026-06-14T21:08:26.445", "lastUpdated" : "2026-06-16T03:23:55.691", "ingestTimestamp" : "2026-06-14T21:08:26.445", "mongoId" : "6a2ebf7d74d8ee00a0e9ab8a", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://labcorp.wd1.myworkdayjobs.com/External/job/Birmingham-AL/Clinical-Laboratory-Technican---Microbiology_2620516", "salaryAnnualMin" : 5000, "salaryAnnualMax" : 5000, "salaryBand" : "<30k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "mid", "dataQualityScore" : 0.7777778, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2c91dd74d8ee00a098436b", "title" : "Performance Specialist", "company" : "LogicMonitor", "salary" : { "min" : 650000.0, "max" : 950000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Junior Performance Specialist in the Technology industry in Bengaluru, India, adjusted for company size and full-time employment." }, "location" : "Bengaluru, Karnataka, India", "locations" : [ "Bengaluru", "Karnataka", "India" ], "timestamp" : "2026-06-16T03:10:05.264", "fingerprint" : "4efc6d1758d279ac51b31b41e33e1a0b0f274572aa8d92d987b1f31ffa4cbcc3", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://www.logicmonitor.com/career/?gh_jid=7923783", "externalId" : "7923783", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Bengaluru", "state" : "Karnataka", "country" : "India", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "12.9767936,77.5900820" } ], "locationText" : "Bengaluru, Karnataka, India", "remoteFriendly" : false, "rawDescription" : "About Us: We love going to work and think you should too. Our team is dedicated to trust, customer obsession, agility, and striving to be better everyday. These values serve as the foundation of our culture, guiding our actions and driving us towards excellence. We foster a culture of performance and recognition, allowing us to transform growth as we enable our employees to do the best work of their careers. This position is located in Pune. You'll be working in a major tech center of Pune, India. Across the globe, our Centers of Energy serve as hubs where we accelerate productivity and collaboration, inspire creativity, and cultivate a culture of connection and celebration. Our teams coordinate their time in Centers of Energy to reflect how they work best. To learn more about life at LogicMonitor, check out our Careers Page. What You'll Do: LogicMonitor® is the AI-first hybrid observability platform powering the next generation of digital infrastructure. LogicMonitor delivers complete visibility and actionable intelligence across on-premises, cloud, and edge environments. By anticipating issues before they strike, optimizing resources in real time, and enabling faster, smarter decisions, LogicMonitor helps IT and business leaders protect margins, accelerate innovation, and deliver exceptional digital experiences without compromise. Our customers love LogicMonitor's ability to bring cloud and traditional IT together into one view, as seen in minimal churn rates, expansion business, and exciting new customer references. In fact, LogicMonitor has received the highest Net Promoter Score of any IT Infrastructure Management provider. LogicMonitor also boasts high employee satisfaction. We have been certified as a Great Place To Work®, and named one of BuiltIn's Best Places to Work for the seventh year in a row! LogicMonitor's Professional Services team partners with global enterprises to monitor, troubleshoot, and optimize end-user digital experience. As a Performance Specialist, you will work at the intersection of internet performance, observability, and customer success, helping organizations identify and resolve issues across the full delivery chain before they impact users. Here's a closer look at this key role: Onboard customers onto the IPM platform following best practices, accelerating time-to-value Proactively monitor and triage customer digital services, surfacing issues before end-user impact Identify performance bottlenecks across internet paths, CDNs, DNS, and third-party dependencies Configure and optimize synthetic test scripts to reflect real user journeys Act as a trusted technical advisor, sharing best practices and product expertise with customers Present performance insights and recommendations in regular customer reviews Collaborate with Engineering, Product, and Support to resolve issues and improve platform capabilities Manage customer expectations and communicate clearly during incidents and escalations What You'll Need: 2+ years in web performance monitoring, observability, or a related technical domain Strong knowledge of DNS, HTTP/S, TLS, CDNs, and the browser rendering pipeline Familiarity with Core Web Vitals, waterfall analysis, and browser DevTools profiling Good understanding of HTML, CSS, and JavaScript as they relate to page performance Understanding of system architecture including servers, load balancers, and networking fundamentals Strong analytical skills with the ability to derive actionable insights from complex data Able to present technical findings to both technical and non-technical audiences Customer-first mindset with a track record of building trusted client relationships Experience using AI tools to enhance productivity, innovation, or problem-solving Click here to read our International Applicant Privacy Notice. LogicMonitor is an Equal Opportunity Employer At LogicMonitor, we believe that innovation thrives when every voice is heard and each individual is empowered to bring their unique perspective. We’re committed to creating a workplace where diversity is celebrated, and all employees feel inspired and supported to contribute their best. For us, equal opportunity means fostering a truly inclusive culture where everyone has the chance to grow and succeed. We don’t just open doors; we invite you to step through and be part of something bigger. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Notice Regarding Use of AI in Hiring We use artificial intelligence tools to assist with reviewing job applications, such as matching skills and experience to job requirements. These tools support, but do not replace, human review. All hiring decisions are made by our recruiting and hiring teams. You may opt out of AI processing at any time, and your application will still be reviewed. To opt out, please contact us at opt.out@logicmonitor.com. By submitting your application, you acknowledge this notice. Our goal is to ensure an accessible and inclusive experience for every candidate. If you need a reasonable accommodation during the application or interview process under applicable local law, please submit a request via this Accommodation Request Form. Know your rights: workplace discrimination is illegal. Please click here to review LogicMonitor’s U. S. Pay Transparency Nondiscrimination Provision.", "summaryDescription" : "Performance Specialist at LogicMonitor", "postedDate" : "2026-06-14T21:32:16.027", "createdAt" : "2026-06-14T21:32:16.027", "lastUpdated" : "2026-06-16T03:10:05.264", "ingestTimestamp" : "2026-06-14T21:32:16.027", "mongoId" : "6a2c91dd74d8ee00a098436b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "sales", "jobSubcategory" : "customer_success", "seniorityLevel" : "Junior", "dataQualityScore" : 0.6666667, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2a63e174d8ee00a0625b32", "title" : "Graduate - Chemical Engineering", "company" : "Waste Management", "industry" : "Logistics And Supply Chain", "salary" : { "min" : 60000.0, "max" : 75000.0, "currency" : "NZD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level Chemical Engineer in Hamilton East, New Zealand, adjusted for the waste management industry and company size." }, "location" : "Hamilton East, Waikato, New Zealand", "locations" : [ "Hamilton East", "Waikato", "New Zealand" ], "timestamp" : "2026-06-15T00:40:44.410", "fingerprint" : "c26bb1792445f772dce3cbecb30d7b62fc396f5c6d0b255911615ef3def84fdf", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/WasteManagement8/6000000001140915-graduate-chemical-engineering-cs", "externalId" : "6000000001140915", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Hamilton East", "state" : "Waikato", "country" : "New Zealand", "continent" : "oc", "source" : "llm", "workMode" : "onsite", "geo" : "-37.7957861,175.2979636" } ], "locationText" : "Hamilton East, Waikato, New Zealand", "employmentType" : "FULL_TIME", "experienceMinYears" : 0, "experienceMaxYears" : 2, "experienceLevel" : "entry", "softSkillsList" : [ "Solution-focused" ], "softSkills" : [ { "name" : "Solution-focused" } ], "coreResponsibilities" : "Gain hands-on experience", "teamCollaboration" : "Cross-functional learning; Collaboration with experts", "domainKnowledge" : "Waste management sector; Sustainability sector", "domainList" : [ "waste-management-sector", "sustainability-sector" ], "domainSpecificKnowledge" : [ "Waste management sector", "Sustainability sector" ], "continuousLearning" : "EMA Training; In-House Training; Mentorship", "innovationCreativity" : "Innovation", "problemSolvingSkills" : "Solution-focused", "outcomesObjectives" : "Make a real impact; Contribute to Aotearoa’s circular economy", "qualificationsBasic" : "Final year of study or recent graduate, New Zealand Citizen or Permanent Resident", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Kick-start your career with us! Are you a recent or soon-to-be Engineering graduate who wants to make a real impact? Join WM New Zealand’s 2027 Graduate Programme and be part of something bigger - shaping a more sustainable Aotearoa through innovation, teamwork, and meaningful mahi. We are looking for a Mechanical or Chemical Engineering graduate to join our 2027 Graduate Programme. This role will be based at our Tirohia Landfill in the Waikato, where you’ll gain hands-on experience in one of WM New Zealand’s key operational sites. About Us | Mō mātou WM New Zealand is Aotearoa’s leading materials recovery, recycling, and waste management provider, with over 1600 team members across 70 locations. Each year, we collect over 1,000,000 tonnes of waste and recycle well over 200,000 tonnes. We are the largest composter in New Zealand, the largest waste-to-energy provider, and have the largest commercial electric fleet in New Zealand, all powered by electricity from waste. As a team, we are constantly looking for new and innovative ways to redirect, neutralise and use waste. Why choose WM New Zealand? | Ngā āhuatanga kei a mātou * Secure your future – You’ll step into a permanent role right from day one. No need to reapply at the end of the programme. * Make a real impact – Contribute to Aotearoa’s circular economy by working with New Zealand’s leader in waste, recycling, and sustainability. * Grow with us – With strong support from our leaders, access to EMA Training, In-House Training and mentorship you’ll gain professional skills that set you up for long-term success. * Earn while you learn – Gain hands-on experience on real-world projects while developing your technical and professional skill set. * Mentorship that matters – Be supported by experienced leaders and connect with a network of past grads and business mentors. * Our values guide everything we do – Together, Safety, Sustainability, Innovation and Service. About the Programme | Te Whiwhinga mahi Our two-year graduate programme begins in February 2027. No two days are the same — you’ll take part in: * Real-world projects that contribute to our sustainability goals * Leadership and communication development through EMA e-learning modules. * In-depth induction week including site tours and executive team sessions. * Cross-functional learning and collaboration with experts and peers. * Personalised mentorship from senior leaders. And the best part? At the end of your two-year journey, you’ll transition into a permanent role with WM New Zealand. ## Qualifications Who we’re looking for We're after motivated, curious, and solution-focused grads who are passionate about sustainability, innovation, and creating real change. You’ll be a great fit if you: * Have a strong interest in the waste and sustainability sector. * Are proactive and resilient and love a challenge. * Think outside the box and enjoy solving problems. * Build strong relationships and enjoy working in a team. * Want to grow your career with purpose. ## Additional Information Eligibility Criteria * You’re in your final year of study or have recently graduated. * You’re a New Zealand Citizen or Permanent Resident * Can commit to a start date of February 2027 Ready to kick-start your career and make a difference? Me Tono Ināianei – Apply Now!”", "summaryDescription" : "Graduate - Chemical Engineering at Waste Management. Gain hands-on experience", "postedDate" : "2026-06-09T19:59:54.000", "createdAt" : "2026-06-12T02:13:36.603", "lastUpdated" : "2026-06-15T00:40:44.410", "ingestTimestamp" : "2026-06-12T02:13:36.603", "mongoId" : "6a2a63e174d8ee00a0625b32", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "50k-75k", "hasSalary" : false, "allSkills" : [ "Solution-focused", "Waste management sector", "Sustainability sector" ], "skillCount" : 3, "jobCategory" : "operations", "jobSubcategory" : "National Organics Manager", "dataQualityScore" : 1.0, "daysOld" : 5, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Waste Management" }, { "id" : "6a2a5dbb74d8ee00a061a163", "title" : "QC Microbiology Manager", "company" : "AbCellera", "industry" : "Biotechnology", "salary" : { "min" : 125000.0, "max" : 175000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Manager in Biotech in Vancouver, Canada, adjusted for seniority and company size." }, "location" : "Vancouver, British Columbia, Canada", "locations" : [ "Vancouver", "British Columbia", "Canada" ], "timestamp" : "2026-06-14T08:45:18.043", "fingerprint" : "81dce8f24c3aaf7d9bb516c4e4bce79619eea2ad3350b357f59525fb112ed529", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/abcellera/jobs/7766549003", "externalId" : "7766549003", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Vancouver", "state" : "British Columbia", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "49.2608724,-123.1139520" } ], "locationText" : "Vancouver, British Columbia, Canada", "minimumEducation" : "Bachelor's", "experienceMinYears" : 10, "experienceLevel" : "Manager", "technicalSkills" : "Microbiology, Microbial methods, Utilities monitoring, Bioburden, Endotoxin, Microbial ID, Water testing", "professionalSkills" : [ "Risk-based testing", "Data integrity", "Inspection readiness" ], "hardSkillsList" : [ "Aseptic practices", "Microbiological best practices", "GMP housekeeping" ], "softSkillsList" : [ "Ownership", "Accountability", "Solutions-focused" ], "hardSkills" : [ { "name" : "Aseptic practices", "level" : "intermediate" }, { "name" : "Microbiological best practices", "level" : "intermediate" }, { "name" : "GMP housekeeping", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Ownership" }, { "name" : "Accountability" }, { "name" : "Solutions-focused" } ], "majorSkills" : "Microbiology leadership, Contamination control, Method troubleshooting", "majorSkillsList" : [ "Microbiology leadership", "Contamination control", "Method troubleshooting" ], "coreResponsibilities" : "Lead day-to-day QC laboratory operations, Provide in-lab presence, Provide technical mentorship, Provide troubleshooting expertise, Support broader QC functions, Serve as QC Microbiology SME, Lead all Microbiology operations, Review micro data packages, Review protocols, Review reports, Review testing documentation, Ensure timely and compliant resolution", "teamCollaboration" : "Collaborate with Analytical Development; Collaborate with Quality Assurance; Collaborate with Materials; Collaborate with Manufacturing", "domainKnowledge" : "GMP environment; Microbiological method strategy; Environmental monitoring; Utilities monitoring; ALCOA++ principles", "domainList" : [ "gmp-environment", "microbiological-method-strategy", "environmental-monitoring", "utilities-monitoring", "alcoa-principles" ], "domainSpecificKnowledge" : [ "GMP environment", "Microbiological method strategy", "Environmental monitoring", "Utilities monitoring", "ALCOA++ principles" ], "communicationSkills" : "Communicate clearly", "documentationSkills" : "Documentation review", "continuousLearning" : "Professional development opportunities", "problemSolvingSkills" : "Troubleshooting expertise; Solutions-focused mindset", "qualificationsBasic" : "10+ years QC microbiology experience, Bachelor's degree in Microbiology, Experience mentoring team members, Experience in regulated (GMP) QC environment, Hands-on Microbiology experience", "qualificationsPreferred" : "Experience in cleanroom/controlled environments", "workSiteFlexibility" : "Onsite", "rawDescription" : "Each of us cares about someone who will need medicines. That’s why our vision is to repeatedly beat the odds to deliver breakthrough medicines to patients that need them. We pursue truth and scientific rigour and have the courage to work at the edge of the unknown. We are looking for a highly skilled QC Microbiology Manager to lead day-to-day QC laboratory operations with a primary focus on Microbiology. You will provide strong in-lab presence, deep technical mentorship, and troubleshooting expertise across microbial methods, EM programs, utilities monitoring, and contamination investigations. In addition to your microbiology leadership, you will support broader QC functions such as stability, sample management, raw materials testing, and analytical assays. How you might spend your days Serving as the QC Microbiology SME for key strategic decisions related to microbiology, including contamination control, microbiological method strategy, environmental monitoring, utilities monitoring, facility readiness, and risk-based testing approaches. Leading all Microbiology operations, including bioburden, endotoxin, microbial ID, growth promotion, EM sampling, water testing, and trending Troubleshooting microbiological assays, contamination events, and EM deviations, ensuring timely and compliant resolution Providing daily in-lab mentorship to the QC team, fostering strong technique, aseptic practices, and microbiological best practices Ensuring microbiology labs and adjacent QC spaces remain inspection-ready, including GMP housekeeping and equipment readiness Reviewing micro data packages, protocols, reports, and testing documentation for accuracy and adherence to ALCOA++ principles Collaborating with Analytical Development, Quality Assurance, Materials, and Manufacturing teammates to ensure smooth operational flow and timely release/testing We'd love to hear from you if You bring deep, hands-on Microbiology experience in a regulated (GMP) QC environment, and are confident in leading microbial methods, EM programs, utilities monitoring, and contamination troubleshooting You have experience mentoring or leading team members working within microbiology labs or cleanroom/controlled environments You have 10+ years of hands-on QC microbiology experience in a GMP setting, in addition to a Bachelor’s degree in Microbiology or a related life sciences field You communicate clearly, collaborate well, and maintain calm, structured decision-making under pressure You demonstrate strong ownership, accountability, and a solutions-focused mindset when supporting analysts or resolving micro-related issues You are organized, detail-oriented, and committed to inspection readiness and data integrity You thrive in an environment requiring in-lab leadership, cross-functional coordination, and prioritization of operational needs What we offer AbCellera’s hiring range for this role is CAD $105,600 - $132,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials. About AbCellera Creating medicines is the most important work we can do. We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline. Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications. We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines. To apply Please submit your application through our website and refer to Job ID 23334 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.", "summaryDescription" : "QC Microbiology Manager at AbCellera. Skills: Microbiology leadership, Contamination control, Method troubleshooting. Lead day-to-day QC laboratory operations. Provide in-lab presence", "postedDate" : "2026-06-11T18:51:22.843", "createdAt" : "2026-06-11T18:51:22.843", "lastUpdated" : "2026-06-14T08:45:18.043", "ingestTimestamp" : "2026-06-11T18:51:22.843", "mongoId" : "6a2a5dbb74d8ee00a061a163", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Aseptic practices", "Microbiological best practices", "GMP housekeeping", "Ownership", "Accountability", "Solutions-focused", "Microbiology leadership", "Contamination control", "Method troubleshooting", "Risk-based testing", "Data integrity", "Inspection readiness", "GMP environment", "Microbiological method strategy", "Environmental monitoring", "Utilities monitoring", "ALCOA++ principles" ], "skillCount" : 17, "jobCategory" : "other", "jobSubcategory" : "quality-control", "dataQualityScore" : 0.8888889, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotechnology" }, { "id" : "6a2a5dbb74d8ee00a061a162", "title" : "QC Microbiology Lead", "company" : "AbCellera", "industry" : "Biotechnology", "salary" : { "min" : 115000.0, "max" : 155000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Lead QC Microbiology position in Vancouver, Canada's biotech industry, adjusted for seniority and company size." }, "location" : "Vancouver, British Columbia, Canada", "locations" : [ "Vancouver", "British Columbia", "Canada" ], "timestamp" : "2026-06-14T07:32:48.269", "fingerprint" : "8a9212e182c846282eb5216a05779fd2d529132d26011e3c0c08314b05523cd9", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/abcellera/jobs/7766550003", "externalId" : "7766550003", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Vancouver", "state" : "British Columbia", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "49.2608724,-123.1139520" } ], "locationText" : "Vancouver, British Columbia, Canada", "minimumEducation" : "Bachelor's", "experienceMinYears" : 10, "experienceMaxYears" : 15, "experienceLevel" : "Lead", "technicalSkills" : "Microbiology, Microbial methods, Bioburden, Endotoxin, Microbial ID, Growth promotion, Water testing, Analytical assays", "professionalSkills" : [ "Quality control", "GMP housekeeping", "Data integrity" ], "hardSkillsList" : [ "Microbial testing", "Assay troubleshooting", "Contamination investigations", "Data review", "Protocol review", "Report review", "Testing documentation review" ], "softSkillsList" : [ "Ownership", "Accountability", "Solutions-focused", "Prioritization" ], "hardSkills" : [ { "name" : "Microbial testing", "level" : "intermediate" }, { "name" : "Assay troubleshooting", "level" : "intermediate" }, { "name" : "Contamination investigations", "level" : "intermediate" }, { "name" : "Data review", "level" : "intermediate" }, { "name" : "Protocol review", "level" : "intermediate" }, { "name" : "Report review", "level" : "intermediate" }, { "name" : "Testing documentation review", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Ownership" }, { "name" : "Accountability" }, { "name" : "Solutions-focused" }, { "name" : "Prioritization" } ], "majorSkills" : "QC Microbiology, GMP environment, Team leadership", "majorSkillsList" : [ "QC Microbiology", "GMP environment", "Team leadership" ], "coreResponsibilities" : "Provide daily in-lab mentorship, Foster technique, Foster aseptic practices, Foster microbiological best practices, Lead Microbiology operations, Troubleshoot microbiological assays, Troubleshoot contamination events, Troubleshoot deviations, Ensure timely resolution, Ensure compliant resolution, Ensure microbiology labs inspection-ready, Ensure adjacent QC spaces inspection-ready, Review micro data packages, Review protocols, Review reports, Review testing documentation, Ensure accuracy, Ensure adherence to ALCOA++, Collaborate with Analytical Development, Collaborate with Quality Assurance, Collaborate with Materials, Collaborate with Manufacturing, Ensure smooth operational flow, Ensure timely release, Ensure timely testing", "teamCollaboration" : "Cross-functional teams; Cross-functional coordination", "domainKnowledge" : "Regulated (GMP) QC; Microbial methods; Utilities monitoring; Contamination investigations; Stability programs; Sample management workflows; Raw materials testing", "domainList" : [ "regulated-gmp-qc", "microbial-methods", "utilities-monitoring", "contamination-investigations", "stability-programs", "sample-management-workflows", "raw-materials-testing" ], "domainSpecificKnowledge" : [ "Regulated (GMP) QC", "Microbial methods", "Utilities monitoring", "Contamination investigations", "Stability programs", "Sample management workflows", "Raw materials testing" ], "communicationSkills" : "Communicate clearly", "documentationSkills" : "Data review; Protocol review; Report review; Testing documentation review", "continuousLearning" : "Professional development opportunities; Scientific mentorship; Technical mentorship", "problemSolvingSkills" : "Troubleshooting; Solutions-focused; Structured decision-making", "qualificationsBasic" : "10+ years hands-on QC microbiology experience, Bachelor's degree in Microbiology or related life sciences, Experience mentoring or leading team members, Experience with stability programs, Experience with sample management workflows, Experience with raw materials testing coordination", "qualificationsPreferred" : "Hands-on microbiology experience in regulated (GMP) QC environment, Confident in leading microbial methods, Confident in leading microbial programs, Confident in leading utilities monitoring, Confident in contamination troubleshooting", "workSiteFlexibility" : "Onsite", "rawDescription" : "Each of us cares about someone who will need medicines. That’s why our vision is to repeatedly beat the odds to deliver breakthrough medicines to patients that need them. We pursue truth and scientific rigour and have the courage to work at the edge of the unknown. We are looking for an experienced, hands-on QC Microbiology Lead - someone who wants to own a program end-to-end - from hands-on testing and troubleshooting to guiding the team around you. This is a primarily bench-based role; you will be in the lab daily, running and troubleshooting assays alongside your team rather than managing from a distance. You will bring deep technical expertise and a strong in-lab presence across microbial methods, EM programs, utilities monitoring, and contamination investigations, while also supporting broader QC functions such as stability, sample management, raw materials testing, and analytical assays. How you might spend your days Providing daily in-lab mentorship to the QC team, fostering strong technique, aseptic practices, and microbiological best practices Leading all Microbiology operations, including bioburden, endotoxin, microbial ID, growth promotion, EM sampling, water testing, and trending Troubleshooting microbiological assays, contamination events, and EM deviations, ensuring timely and compliant resolution Ensuring microbiology labs and adjacent QC spaces remain inspection-ready, including GMP housekeeping and equipment readiness Reviewing micro data packages, protocols, reports, and testing documentation for accuracy and adherence to ALCOA++ principles Collaborating with Analytical Development, Quality Assurance, Materials, and Manufacturing teammates to ensure smooth operational flow and timely release/testing We'd love to hear from you if You bring deep, hands-on microbiology experience in a regulated (GMP) QC environment, and are confident in leading microbial methods, EM programs, utilities monitoring, and contamination troubleshooting You have experience mentoring or leading team members working within microbiology labs or cleanroom/controlled environments You have 10+ years of hands-on QC microbiology experience in a GMP setting, in addition to a Bachelor’s degree in Microbiology or a related life sciences field You communicate clearly, collaborate well, and maintain calm, structured decision-making under pressure You demonstrate strong ownership, accountability, and a solutions-focused mindset when supporting analysts or resolving micro-related issues You are organized, detail-oriented, and committed to inspection readiness and data integrity You thrive in an environment requiring in-lab leadership, cross-functional coordination, and prioritization of operational needs You have experience with stability programs, sample management workflows, and raw materials testing coordination What we offer AbCellera’s hiring range for this role is CAD $105,600 - $132,000 annually, commensurate with your education and job-related knowledge, skills, and experience. In addition to base salary, we offer equity, annual bonus dependent on team and company performance, and a 6% (non-match) RRSP contribution. You will have a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority. And you’ll find a strong sense of community and connections across AbCellera through our work, clubs, and socials. About AbCellera Creating medicines is the most important work we can do. We are a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology, women’s health, immunology, and oncology. We have built a platform for advancing antibody drug programs from target to clinic, and we are using it to build our internal pipeline. Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications. We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That’s why we hire for character and intelligence, not just for CVs or experience. We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines. To apply Please submit your application through our website and refer to Job ID 23334 in your cover letter. We receive a large volume of applications and are only able to contact those who are selected for an interview. All communication from our Talent Discovery team will come from an @abcellera.com email address.", "summaryDescription" : "QC Microbiology Lead at AbCellera. Skills: QC Microbiology, GMP environment, Team leadership. Provide daily in-lab mentorship. Foster technique", "postedDate" : "2026-06-11T18:00:52.141", "createdAt" : "2026-06-11T18:00:52.141", "lastUpdated" : "2026-06-14T07:32:48.269", "ingestTimestamp" : "2026-06-11T18:00:52.141", "mongoId" : "6a2a5dbb74d8ee00a061a162", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Microbial testing", "Assay troubleshooting", "Contamination investigations", "Data review", "Protocol review", "Report review", "Testing documentation review", "Ownership", "Accountability", "Solutions-focused", "Prioritization", "QC Microbiology", "GMP environment", "Team leadership", "Quality control", "GMP housekeeping", "Data integrity", "Regulated (GMP) QC", "Microbial methods", "Utilities monitoring", "Stability programs", "Sample management workflows", "Raw materials testing" ], "skillCount" : 23, "jobCategory" : "other", "jobSubcategory" : "quality-control", "dataQualityScore" : 0.8888889, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotechnology" }, { "id" : "6a2ebf7d74d8ee00a0e9abad", "title" : "Microbiology Lab Assistant", "company" : "Labcorp", "salary" : { "min" : 46500.0, "max" : 63500.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Microbiology Lab Assistant in Phoenix, AZ, adjusted for the healthcare industry and company size." }, "location" : "United States of America", "locations" : [ "United States of America" ], "timestamp" : "2026-06-16T03:09:32.276", "fingerprint" : "d120b2e41fc58a98c934a7a30707bc18f653066aaa508664bb3b818dee95345e", "source" : "workday", "language" : "en", "applyUrl" : "https://labcorp.wd1.myworkdayjobs.com/External/job/Phoenix-AZ/Microbiology-Lab-Assistant_2617351", "externalId" : "2617351", "industryFunction" : { }, "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "city" : "Phoenix", "state" : "Arizona", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "33.4484367,-112.0741410" } ], "locationText" : "Phoenix, Arizona, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "High School Diploma or GED equivalent", "experienceMinYears" : 2, "remoteFriendly" : false, "rawDescription" : "Labcorp is seeking a Lab Assistant to join our team in **Phoenix, AZ.** **Work Schedule:** Evening Shift, Tuesday - Saturday, 2:00 pm - 10:30 pm. Overtime required as need. **Job Responsibilities:** * Receive and sort clinical lab specimens * Prepare specimens for testing and analysis * Scan and/or data entry of specimen and patient information * Ensure all lab equipment is working properly and perform minor instrumentation maintenance * Troubleshoot any specimen related issues * Replenish test bench supplies as needed * Maintain a clean and safe work environment * Complete record logs and other administrative duties as requested * Follow all Standard Operating Procedures to ensure safety and quality standards **Minimum Qualifications:** * High School Diploma or GED equivalent * Two years or more of experience in the healthcare industry, such as a physician's office, clinic or hospital * Two years or more of experience in a medical/clinical laboratory **Preferred Qualification:** * Current or prior Labcorp experience * Two years or more of experience in an assembly or manufacturing production environment **Additional Job Standards:** * Comfortability with handling biological specimens * Able to accurately identify specimens * Basic computer knowledge and data entry skills * High level of attention to detail with the ability to prioritize and multitask * Able to work in a fast-paced production environment and meet established turn-around times * Strong communication skills; both written and verbal * Able to sit and/or stand for extended periods of time * Able to pass a standardized color blindness test * Able to work overtime as needed _At Labcorp we have a passion in helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career step!_ Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please [_click here_](https://careers.labcorp.com/global/en/us-rewards-and-wellness).**** **Labcorp is proud to be an Equal Opportunity Employer:** Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. **We encourage all to apply** If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our [accessibility site](https://careers.labcorp.com/global/en/accessibility) or contact us at [Labcorp Accessibility.](mailto:Disability_apply@LabCorp.com) For more information about how we collect and store your personal data, please see our [Privacy Statement](https://www.labcorp.com/about/web-privacy-policy).", "summaryDescription" : "Microbiology Lab Assistant at Labcorp", "postedDate" : "2026-06-11T21:28:55.421", "createdAt" : "2026-06-14T21:28:55.347", "lastUpdated" : "2026-06-16T03:09:32.276", "ingestTimestamp" : "2026-06-14T21:28:55.347", "mongoId" : "6a2ebf7d74d8ee00a0e9abad", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://labcorp.wd1.myworkdayjobs.com/External/job/Phoenix-AZ/Microbiology-Lab-Assistant_2617351", "salaryAnnualMin" : 46500, "salaryAnnualMax" : 63500, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "mid", "dataQualityScore" : 0.7777778, "daysOld" : 4, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a305a7ff292fd229cf51d10", "title" : "Performance Marketing Manager", "company" : "AfterShip", "industry" : "SaaS", "salary" : { "min" : 102000.0, "max" : 162500.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Toronto, Ontario, Canada", "locations" : [ "Toronto", "Ontario", "Canada", "Texas", "United States" ], "timestamp" : "2026-06-16T08:54:32.856", "fingerprint" : "56e6aed29d2f5ed50854fd818b00f20658f6f386e2b62d9c1676fe2350c9c151", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/aftership/jobs/6029595004", "externalId" : "6029595004", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Toronto", "state" : "Ontario", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "43.6534817,-79.3839347" } ], "locationText" : "Toronto, Ontario, Canada", "employmentType" : "FULL_TIME", "experienceLevel" : "Manager", "professionalSkills" : [ "Brand strategy", "Customer acquisition", "Campaign management", "Growth metrics" ], "majorSkills" : "Brand strategy, Customer acquisition, Campaign management, Growth metrics", "majorSkillsList" : [ "Brand strategy", "Customer acquisition", "Campaign management", "Growth metrics" ], "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "About Us AfterShip, a Great Place to Work Certified company, is transforming the global eCommerce landscape. Founded in 2012, AfterShip is a post-purchase SaaS company on a mission to build the world’s leading automation platform for ecommerce merchants. AfterShip unifies shipping & labels, order tracking, AI predictive delivery, and returns management into one system—giving merchants a single place to manage and automate everything that happens after checkout. By centralizing these workflows, AfterShip enables merchants to reduce customer support inquiries, deliver a more reliable and engaging customer experiences, and unlock incremental revenue at every post-purchase touchpoint. AfterShip integrates seamlessly with eCommerce platforms including Shopify and TikTok Shop, and connects with more than 1,200 carriers worldwide. Today, over 20,000 businesses—including Samsung, Gymshark, Mejuri, Dr. Squatch and Alo Yoga—rely on AfterShip to turn every post-purchase moment into an opportunity to build trust, reduce costs, and drive repeat purchases. Built for a global market from day one, AfterShip operates with an engineering-driven, internationally distributed team. The company employs more than 450 people across 8 offices, spanning North America, Europe, and Asia, and representing over 20 cities worldwide. Your Mission: You’ll own and scale paid media at AfterShip, serving as the technical expert behind the engine that drives top-of-funnel pipeline growth across our ICP accounts. From bidding strategy and audience targeting to creative testing and conversion analysis, you’ll lead performance across channels including Google Search, LinkedIn, paid social, retargeting, and emerging acquisition channels. You’ll inherit an existing paid media foundation with the opportunity to take it to the next level, improving unit economics, expanding the channel mix through thoughtful experimentation, and building a consistent pipeline engine for sales to convert. This role comes with significant autonomy, growing budgets, and direct support from the VP of Marketing, giving you the opportunity to shape the future of paid acquisition at AfterShip. You’ll report directly to the VP of Marketing and work closely with Marketing Ops, Vertical Marketing, Content, and Brand to execute high-performing, integrated demand generation campaigns. What You'll Do: Own always-on ICP campaigns across Google Search, LinkedIn, paid social, and retargeting, including audience targeting, creative testing, bidding strategy, and budget pacing. Drive paid amplification for product launches, events, content releases, and brand campaigns, ensuring campaigns reach the right audiences at the right time. Continuously optimize performance through hypothesis-driven A/B testing across creative, audiences, landing pages, and bidding strategies, while documenting insights and learnings that help improve overall marketing effectiveness. Take ownership of paid media pipeline performance, ensuring media spend translates into demos booked and pipeline generated. Partner closely with Marketing Ops to maintain accurate attribution, reporting, and UTM hygiene. Recommend and manage monthly budget allocation across channels based on performance data, pipeline impact, and growth opportunities. Who We're Looking For: Deep expertise in B2B paid media, ideally in SaaS, with 5+ years of experience owning paid channel performance end-to-end. Strong hands-on experience with Google and LinkedIn Ads. Experience with paid social, retargeting, and app store advertising is a plus. Comfortable operating campaigns directly within ad platforms, not just managing external agencies. A pipeline-first marketer who measures success through MQLs, demos held, pipeline generated, and revenue impact. A disciplined experimenter who can develop hypotheses, run structured tests, interpret results confidently, and scale what works. Strong understanding of marketing attribution, conversion tracking, UTMs, and campaign measurement fundamentals. Direct, thoughtful, and intellectually rigorous. You welcome feedback, communicate clearly, and challenge assumptions constructively when needed. A strong collaborator who builds trust across functions and time zones, communicates proactively in async environments, and works effectively in distributed teams. At AfterShip, we know great talent doesn’t always fit every requirement. If you’re passionate about our mission and believe you can make an impact, we encourage you to apply. Why You Should Join Us: Great Place to Work Certified: We’ve been recognized for our inclusive, values-driven culture that celebrates diversity and collaboration. Innovative & Inclusive Culture: Started by our software engineer-turned-CEO, AfterShip is built on curiosity, creativity, and collaboration. We’re a passionate, global team of problem solvers who put egos aside to innovate together. We take immense pride in fostering a culture that’s inclusive, which has allowed us to surround ourselves with the industry's most talented professionals. Ambitious Mission with Real Impact: Join us in transforming eCommerce by making buying and selling easier for everyone. It’s one of the most dynamic spaces in tech, with limitless opportunities to innovate and grow. Thrive & Grow: There’s no ceiling to what you can achieve or learn here. We’re committed to empowering your career while advancing together as a company. Flexible Work Setup: We’re a remote-first team, meaning by default that employees work from home or on a hybrid-flexible basis in our hub locations (i.e., Toronto, Austin, Barcelona). You’re empowered to choose a work setup that works best for you and your team. With flexible hours depending on your time zone, you’ll be able to have a schedule that fits your working style and the requirements of your role. Perks: Competitive compensation Remote-first work setup Healthcare coverage offered from day 1 Retirement plans including company match Unlimited PTO Annual learning & wellness benefit Monthly book perk Career progression & professional development Salary range for this role: USD$102,000 - USD$162,500 We are an equal opportunity employer and provide accommodations upon request throughout the recruitment process, in accordance with local legislation. Please let us know if you require any support, and we’ll work with you to meet your needs.", "summaryDescription" : "Performance Marketing Manager at AfterShip. Skills: Brand strategy, Customer acquisition, Campaign management, Growth metrics", "postedDate" : "2026-06-15T23:24:39.241", "createdAt" : "2026-06-15T23:24:39.241", "lastUpdated" : "2026-06-16T08:54:32.856", "ingestTimestamp" : "2026-06-15T23:24:39.241", "mongoId" : "6a305a7ff292fd229cf51d10", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Brand strategy", "Customer acquisition", "Campaign management", "Growth metrics" ], "skillCount" : 4, "jobCategory" : "marketing", "jobSubcategory" : "growth", "seniorityLevel" : "Manager", "dataQualityScore" : 1.0, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "SaaS", "llmIndustryConfidence" : 0.98 }, { "id" : "6a305a7ff292fd229cf51d11", "title" : "Performance Marketing Manager", "company" : "AfterShip", "industry" : "SaaS", "salary" : { "min" : 88000.0, "max" : 124000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Toronto, Ontario, Canada", "locations" : [ "Toronto", "Ontario", "Canada", "Texas", "United States" ], "timestamp" : "2026-06-16T08:12:54.316", "fingerprint" : "bfaa7c9183782b2b9c8f0831941ada6cb49b40bdbfa2bc87d8b37f1ad6cad21b", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/aftership/jobs/6029593004", "externalId" : "6029593004", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Toronto", "state" : "Ontario", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "43.6534817,-79.3839347" } ], "locationText" : "Toronto, Ontario, Canada", "employmentType" : "FULL_TIME", "experienceLevel" : "Manager", "majorSkills" : "Brand strategy, Customer acquisition, Campaign management, Growth metrics", "majorSkillsList" : [ "Brand strategy", "Customer acquisition", "Campaign management", "Growth metrics" ], "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "About Us AfterShip, a Great Place to Work Certified company, is transforming the global eCommerce landscape. Founded in 2012, AfterShip is a post-purchase SaaS company on a mission to build the world’s leading automation platform for ecommerce merchants. AfterShip unifies shipping & labels, order tracking, AI predictive delivery, and returns management into one system—giving merchants a single place to manage and automate everything that happens after checkout. By centralizing these workflows, AfterShip enables merchants to reduce customer support inquiries, deliver a more reliable and engaging customer experiences, and unlock incremental revenue at every post-purchase touchpoint. AfterShip integrates seamlessly with eCommerce platforms including Shopify and TikTok Shop, and connects with more than 1,200 carriers worldwide. Today, over 20,000 businesses—including Samsung, Gymshark, Mejuri, Dr. Squatch and Alo Yoga—rely on AfterShip to turn every post-purchase moment into an opportunity to build trust, reduce costs, and drive repeat purchases. Built for a global market from day one, AfterShip operates with an engineering-driven, internationally distributed team. The company employs more than 450 people across 8 offices, spanning North America, Europe, and Asia, and representing over 20 cities worldwide. Your Mission: You’ll own and scale paid media at AfterShip, serving as the technical expert behind the engine that drives top-of-funnel pipeline growth across our ICP accounts. From bidding strategy and audience targeting to creative testing and conversion analysis, you’ll lead performance across channels including Google Search, LinkedIn, paid social, retargeting, and emerging acquisition channels. You’ll inherit an existing paid media foundation with the opportunity to take it to the next level, improving unit economics, expanding the channel mix through thoughtful experimentation, and building a consistent pipeline engine for sales to convert. This role comes with significant autonomy, growing budgets, and direct support from the VP of Marketing, giving you the opportunity to shape the future of paid acquisition at AfterShip. You’ll report directly to the VP of Marketing and work closely with Marketing Ops, Vertical Marketing, Content, and Brand to execute high-performing, integrated demand generation campaigns. What You'll Do: Own always-on ICP campaigns across Google Search, LinkedIn, paid social, and retargeting, including audience targeting, creative testing, bidding strategy, and budget pacing. Drive paid amplification for product launches, events, content releases, and brand campaigns, ensuring campaigns reach the right audiences at the right time. Continuously optimize performance through hypothesis-driven A/B testing across creative, audiences, landing pages, and bidding strategies, while documenting insights and learnings that help improve overall marketing effectiveness. Take ownership of paid media pipeline performance, ensuring media spend translates into demos booked and pipeline generated. Partner closely with Marketing Ops to maintain accurate attribution, reporting, and UTM hygiene. Recommend and manage monthly budget allocation across channels based on performance data, pipeline impact, and growth opportunities. Who We're Looking For: Deep expertise in B2B paid media, ideally in SaaS, with 5+ years of experience owning paid channel performance end-to-end. Strong hands-on experience with Google and LinkedIn Ads. Experience with paid social, retargeting, and app store advertising is a plus. Comfortable operating campaigns directly within ad platforms, not just managing external agencies. A pipeline-first marketer who measures success through MQLs, demos held, pipeline generated, and revenue impact. A disciplined experimenter who can develop hypotheses, run structured tests, interpret results confidently, and scale what works. Strong understanding of marketing attribution, conversion tracking, UTMs, and campaign measurement fundamentals. Direct, thoughtful, and intellectually rigorous. You welcome feedback, communicate clearly, and challenge assumptions constructively when needed. A strong collaborator who builds trust across functions and time zones, communicates proactively in async environments, and works effectively in distributed teams. At AfterShip, we know great talent doesn’t always fit every requirement. If you’re passionate about our mission and believe you can make an impact, we encourage you to apply. Why You Should Join Us: Great Place to Work Certified: We’ve been recognized for our inclusive, values-driven culture that celebrates diversity and collaboration. Innovative & Inclusive Culture: Started by our software engineer-turned-CEO, AfterShip is built on curiosity, creativity, and collaboration. We’re a passionate, global team of problem solvers who put egos aside to innovate together. We take immense pride in fostering a culture that’s inclusive, which has allowed us to surround ourselves with the industry's most talented professionals. Ambitious Mission with Real Impact: Join us in transforming eCommerce by making buying and selling easier for everyone. It’s one of the most dynamic spaces in tech, with limitless opportunities to innovate and grow. Thrive & Grow: There’s no ceiling to what you can achieve or learn here. We’re committed to empowering your career while advancing together as a company. Flexible Work Setup: We’re a remote-first team, meaning by default that employees work from home or on a hybrid-flexible basis in our hub locations (i.e., Toronto, Austin, Barcelona). You’re empowered to choose a work setup that works best for you and your team. With flexible hours depending on your time zone, you’ll be able to have a schedule that fits your working style and the requirements of your role. Perks: Competitive compensation Hybrid-flexible work setups Healthcare coverage offered from day 1 Retirement plans including company match Unlimited PTO Annual learning & wellness benefit Monthly book perk Career progression & professional development In-office lunch and commuter benefits for those located in our hub locations Salary range for this role: CAD$88,000 - CAD$124,000 We are an equal opportunity employer and provide accommodations upon request throughout the recruitment process, in accordance with local legislation. Please let us know if you require any support, and we’ll work with you to meet your needs. We believe in hiring right over hiring fast. While timelines may vary, we’re looking to fill this role as soon as possible. Our hiring process uses AI to help with initial resume screening and to support interview note-taking. These tools help our team stay organized and fair, but all hiring decisions are made by people. This job posting is for a new position.", "summaryDescription" : "Performance Marketing Manager at AfterShip. Skills: Brand strategy, Customer acquisition, Campaign management, Growth metrics", "postedDate" : "2026-06-15T23:23:10.138", "createdAt" : "2026-06-15T23:23:10.138", "lastUpdated" : "2026-06-16T08:12:54.316", "ingestTimestamp" : "2026-06-15T23:23:10.138", "mongoId" : "6a305a7ff292fd229cf51d11", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Brand strategy", "Customer acquisition", "Campaign management", "Growth metrics" ], "skillCount" : 4, "jobCategory" : "marketing", "jobSubcategory" : "growth", "seniorityLevel" : "Manager", "dataQualityScore" : 1.0, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "SaaS", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2eb40374d8ee00a0e7f69c", "title" : "RN OR", "company" : "Corewell Health", "industry" : "Healthcare", "salary" : { "min" : 78500.0, "max" : 105500.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for RN OR in Grand Rapids, MI, adjusted for mid-seniority and healthcare industry." }, "location" : "Grand Rapids, MI", "locations" : [ "Grand Rapids, MI", "United States of America" ], "timestamp" : "2026-06-16T01:02:36.060", "fingerprint" : "285f5219a0f15214e002b84a714aa6b97308faab4e938988ac987ae09cc7cb88", "source" : "workday", "language" : "en", "applyUrl" : "https://spectrumhealth.wd5.myworkdayjobs.com/CorewellHealthCareers/job/Grand-Rapids-MI/RN-OR_R217545", "externalId" : "R217545", "industryFunction" : { }, "locationPoint" : "41.412,-83.86439", "structuredLocations" : [ { "city" : "Grand Rapids", "state" : "Michigan", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.9632425,-85.6678639" } ], "locationText" : "Grand Rapids, Michigan, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Associate's", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## **About this unit** The Butterworth OR is a level 1 trauma center and teaching hospital. The department consists of twenty-one (21) operating rooms that provide 24/7 patient care including the support of procedures across the medical center in other departments. Our multidisciplinary team of providers including anesthesiologists, surgeons, nurses, surgical technicians, and support technicians collaborate to provide high quality, safe patient care. The surgical team is trained in many specialties including but not limited to orthopedic and neurosurgical trauma, acute care surgery, women’s health, urology, oncology, and general surgery. The Butterworth operative department utilizes many care delivery technologies such as DaVinci and Rosa robotics, Stealth guided navigation, and intra-operative MRI technology. All of this combines to maintain our focus on safe, efficient patient-centered care**.** ## **About Butterworth Hospital** Right in the heart of Grand Rapids, you’ll find a nationally recognized hospital for patient quality and safety and the regional leader in full-service hospitals. Since 1873, we have been growing and building a reputation of excellence in care, diagnostics, treatment, prevention and education. It is the flagship hospital for Corewell Health Grand Rapids Hospitals. **Scope of work** The RN, under the ANA scope of practice utilizes the framework of the nursing process to provide professional nursing care by incorporating patient-family centered care principles to assess, plan, implement, evaluate, and discharge. The RN provides quality patient care under the direction of the Nurse Leader according to Corewell Health policies and procedures and recognizes the impact of nursing care and patient/family partnerships on patient outcomes. The RN partners with and utilizes patient/family input and goals in planning plan of care and develops teaching strategies for patient/family; documents education and learning appropriately in health record. **Qualifications** * Associates in Nursing Required * Bachelors in Nursing Required within 5 years * MI Registered Nurse (RN) Required * AHA or ARC Basic Life Support (BLS) Required within 90 days * 6-12+ months of RN experience preferred ## How Corewell Health cares for you * Comprehensive benefits package to meet your financial, health, and work/life balance goals. Learn more [here](https://careers.corewellhealth.org/us/en/benefits-new). * On-demand pay program powered by Payactiv * Discounts directory with deals on the things that matter to you, like restaurants, phone plans, spas, and more! * Optional identity theft protection, home and auto insurance * Traditional and Roth retirement options with service contribution and match savings * Eligibility for benefits is determined by employment type and status **Primary Location** SITE - Butterworth Hospital - 100 Michigan St NE - Grand Rapids **Department Name** Operating Room Butterworth - Grand Rapids Hosp **Employment Type** Full time **Shift** Day (United States of America) **Weekly Scheduled Hours** 40 **Hours of Work** 7:00am-5:30pm **Days Worked** Variable **Weekend Frequency** Variable weekends ********CURRENT COREWELL HEALTH TEAM MEMBERS – Please apply through Find Jobs from your Workday team member account. This career site is for Non-Corewell Health team members only.******** _Corewell Health is committed to providing a safe environment for our team members, patients, visitors, and community. We require a drug-free workplace and require team members to comply with the MMR, Varicella, Tdap, and Influenza vaccine requirement if in an on-site or hybrid workplace category. We are committed to supporting prospective team members who require reasonable accommodations to participate in the job application process, to perform the essential functions of a job, or to enjoy equal benefits and privileges of employment due to a disability, pregnancy, or sincerely held religious belief._ _Corewell Health grants equal employment opportunity to all qualified persons without regard to race, color, national origin, sex, disability, age, religion, genetic information, marital status, height, weight, gender, pregnancy, sexual orientation, gender identity or expression, veteran status, or any other legally protected category._ _An interconnected, collaborative culture where all are encouraged to bring their whole selves to work, is vital to the health of our organization. As a health system, we advocate for equity as we care for our patients, our communities, and each other. From workshops that develop cultural intelligence, to our inclusion resource groups for people to find community and empowerment at work, we are dedicated to ongoing resources that advance our values of diversity, equity, and inclusion in all that we do. We invite those that share in our commitment to join our team._ _You may request assistance in completing the application process by calling 616.486.7447._", "summaryDescription" : "RN OR at Corewell Health", "postedDate" : "2026-06-12T21:07:07.292", "createdAt" : "2026-06-14T21:07:07.249", "lastUpdated" : "2026-06-16T01:02:36.060", "ingestTimestamp" : "2026-06-14T21:07:07.249", "mongoId" : "6a2eb40374d8ee00a0e7f69c", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://spectrumhealth.wd5.myworkdayjobs.com/CorewellHealthCareers/job/Grand-Rapids-MI/RN-OR_R217545", "salaryAnnualMin" : 78500, "salaryAnnualMax" : 105500, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "healthcare", "jobSubcategory" : "support", "seniorityLevel" : "mid", "dataQualityScore" : 0.7777778, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 } ], "status" : 200, "message" : "perform routine chemical immunochemical biological or microbiological assays jobs", "metadata" : { "title" : "perform routine chemical immunochemical biological or microbiological assays" }, "pagination" : { "page" : 0, "limit" : 50, "totalCount" : 6257, "totalPages" : 126, "hasNext" : true, "hasPrevious" : false } }

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