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US biopharma, CRO, academic, or assay development customer segments." ], "hardSkillsList" : [ "bioassay workflows", "reagent-based assays", "cell-based assays", "reporter systems", "plate-based detection technologies" ], "softSkillsList" : [ "collaboration" ], "hardSkills" : [ { "name" : "bioassay workflows", "level" : "intermediate" }, { "name" : "reagent-based assays", "level" : "intermediate" }, { "name" : "cell-based assays", "level" : "intermediate" }, { "name" : "reporter systems", "level" : "intermediate" }, { "name" : "plate-based detection technologies", "level" : "intermediate" } ], "softSkills" : [ { "name" : "collaboration" } ], "majorSkills" : "product management, product marketing, market analysis, customer needs, cross-functional collaboration", "majorSkillsList" : [ "product management, product marketing, market analysis, customer needs, cross-functional collaboration" ], "coreResponsibilities" : "Understand customer needs and workflows across bioassays, functional assays, reagent-based assays, and related application areas. Conduct voice-of-customer interviews with biopharma, CRO, academic, and assay development customers. Analyze market trends, customer segments, competitive landscape, pricing dynamics, and application requirements. Support product positioning, messaging, value proposition, and differentiation. Work cross-functionally with R&D, sales, marketing, and regional teams to translate market needs into product and commercial plans. Develop go-to-market materials, sales tools, customer-facing content, and launch support plans. Identify KOLs, key accounts, and collaboration opportunities to support market development.", "teamCollaboration" : "Work cross-functionally with R&D, sales, marketing, and regional teams.", "projectManagementSkills" : [ "launch readiness" ], "communicationSkills" : "communication; analytical", "problemSolvingSkills" : "product positioning; launch planning; sales enablement", "specialRequirements" : "Candidate must reside within the United States.", "outcomesObjectives" : "Drive commercial adoption of products.", "qualificationsBasic" : "5+ years of experience in product management, product marketing, market development, or business development in life sciences tools, reagents, assays, or biotech solutions. Familiarity with bioassay workflows, reagent-based assays, cell-based assays, reporter systems, or plate-based detection technologies. Experience with VOC, market analysis, competitive assessment, product positioning, launch planning, and sales enablement. commercial sense and ability to translate customer needs into actionable product and marketing strategy. Excellent communication, analytical, and cross-functional collaboration skills.", "qualificationsPreferred" : "Supporting assay, reagent, or molecular biology product portfolios. Prior experience in new product launch, market development, or application-driven product marketing. Good understanding of US biopharma, CRO, academic, or assay development customer segments. Experience working with cross-functional global teams.", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "About GenScript GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. We are looking for a US-based Product Management / Product Marketing professional to support assay-related product initiatives for life science and biopharma applications. This role will focus on customer workflow understanding, market insights, product positioning, launch readiness, and commercial adoption. This role can be fully remote, but the candidate must reside within the United States. Key Responsibilities Understand customer needs and workflows across bioassays, functional assays, reagent-based assays, and related application areas. Conduct voice-of-customer interviews with biopharma, CRO, academic, and assay development customers. Analyze market trends, customer segments, competitive landscape, pricing dynamics, and application requirements. Support product positioning, messaging, value proposition, and differentiation. Work cross-functionally with R&D, sales, marketing, and regional teams to translate market needs into product and commercial plans. Develop go-to-market materials, sales tools, customer-facing content, and launch support plans. Identify KOLs, key accounts, and collaboration opportunities to support market development. Requirements 5+ years of experience in product management, product marketing, market development, or business development in life sciences tools, reagents, assays, or biotech solutions. Familiarity with bioassay workflows, reagent-based assays, cell-based assays, reporter systems, or plate-based detection technologies. Experience with VOC, market analysis, competitive assessment, product positioning, launch planning, and sales enablement. Strong commercial sense and ability to translate customer needs into actionable product and marketing strategy. Excellent communication, analytical, and cross-functional collaboration skills. Preferred Experience supporting assay, reagent, or molecular biology product portfolios. Prior experience in new product launch, market development, or application-driven product marketing. Good understanding of US biopharma, CRO, academic, or assay development customer segments. Experience working with cross-functional global teams. #LI-EB1 #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.", "summaryDescription" : "Product Manager, Gene to Protein Lab Essentials at GenScript/ProBio. Skills: product management, product marketing, market analysis, customer needs, cross-functional collaboration. Understand customer needs and workflows across bioassays, functional assays, reagent-based assays, and related application areas. Conduct voice-of-customer interviews with biopharma, CRO, academic, and assay development customers. Analyze market trends, customer segments, competitive landscape, pricing dynamics, and a", "postedDate" : "2026-06-14T21:42:16.439", "createdAt" : "2026-06-14T21:42:16.439", "lastUpdated" : "2026-06-15T11:16:31.059", "ingestTimestamp" : "2026-06-14T21:42:16.439", "mongoId" : "6a2cd91574d8ee00a0a47249", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "hasSalary" : false, "allSkills" : [ "bioassay workflows", "reagent-based assays", "cell-based assays", "reporter systems", "plate-based detection technologies", "collaboration", "product management, product marketing, market analysis, customer needs, cross-functional collaboration", "Life sciences tools, reagents, assays, or biotech solutions. US biopharma, CRO, academic, or assay development customer segments.", "launch readiness" ], "skillCount" : 9, "jobCategory" : "product", "jobSubcategory" : "product_management", "seniorityLevel" : "Senior", "dataQualityScore" : 0.8888889, "daysOld" : 0, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.98 }, { "id" : "69dde45c2beec4dd3d9a3fa7", "title" : "Postdoctoral Fellow or Staff Scientist - Protein Chemistry, Crystallography and Structure Determination", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 34.0, "max" : 123.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Research" ], "timestamp" : "2026-06-16T03:10:32.877", "fingerprint" : "f9bb2bf4fd1b7bae403c5a58684d192f724bf1b71b175510bc8b0ddf458ce990", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=140141", "externalId" : "140141", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Duarte", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.1394513,-117.9772873" } ], "locationText" : "Duarte, California, United States", "minimumEducation" : "PhD", "remoteFriendly" : false, "rawDescription" : "Thank you for your interest. Please note, the purpose of this posting is to recruit for on-going and future positions. Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope , where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research. The John Williams research lab at City of Hope is seeking a Postdoctoral Fellow or a Staff Scientist to join an innovative team. Our research primarily focuses on structural and biophysical methods to identify sources of energy additivity and multivalency in macromolecular complexes and use these properties to develop new tools and novel therapeutics. As a successful candidate, you will: · Determine structure of modified antibodies with immune receptors · Apply yeast display to stabilize and subsequent deimmunize proteases · Create additional antibody variants to maximize the therapeutic activity in a clinical setting Your qualifications should include: · Ph.D. degree chemistry, biochemistry, structural biology, biophysics or a related discipline is required. · Knowledge of protein engineering (cloning, expression, purification), crystallography (crystallization, optimization, data collection and structure determination), biochemistry (enzyme kinetics) and biophysics (Surface Plasmon Resonance, Iosthermal Ttitration Calorimetry Additional Information: · To apply to the position, please send your CV or resume to Dr. John Williams at jcwilliams@coh.org for consideration. · Candidates will be assessed for the suitable level based on their relevant experience. · Postdoctoral Fellow - Pay Rate: $34.00 – $37.54 · Staff Scientist – Pay Rate: $38.67 – $123.37 City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here . United States-California-Duarte", "summaryDescription" : "Postdoctoral Fellow or Staff Scientist - Protein Chemistry, Crystallography and Structure Determination at City of Hope", "createdAt" : "2026-06-14T20:42:37.783", "lastUpdated" : "2026-06-16T03:10:32.877", "ingestTimestamp" : "2026-06-14T20:42:37.783", "mongoId" : "69dde45c2beec4dd3d9a3fa7", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 70720, "salaryAnnualMax" : 255840, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 0.5555556, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2b2ebd74d8ee00a0785480", "title" : "CDL A - Ag Protein (nights)", "company" : "Smithfield", "salary" : { "min" : 21.75, "max" : 21.75, "currency" : "USD", "frequency" : "yearly" }, "location" : "Magnolia, NC", "locations" : [ "Magnolia, NC", "United States of America" ], "certifications" : [ "CDL A" ], "timestamp" : "2026-06-14T22:55:03.485", "fingerprint" : "cf99e909900dfc7df0c76b5f275b9df749be80c83bb8fdd7b375a57a1ee7acdd", "source" : "workday", "language" : "en", "applyUrl" : "https://smithfieldfoods.wd1.myworkdayjobs.com/Careers/job/Magnolia-NC/ADU-CDL-Driver-Trainee_R-2026-7235", "externalId" : "R-2026-7235", "locationPoint" : "39.94984,-74.66071", "structuredLocations" : [ { "city" : "Magnolia", "state" : "North Carolina", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.8965563,-78.0541545" } ], "locationText" : "Magnolia, North Carolina, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 1, "hardSkillsList" : [ "Driving", "Route planning" ], "hardSkills" : [ { "name" : "Driving", "level" : "intermediate" }, { "name" : "Route planning", "level" : "intermediate" } ], "majorSkills" : "CDL Driving, Route operations", "majorSkillsList" : [ "CDL Driving", "Route operations" ], "coreResponsibilities" : "Drive ADU truck on route, Service ADU containers, Transport product to rendering facility, Complete assigned route safely, Perform pre-trip inspections, Perform post trip inspections, Collaborate with other drivers, Collaborate with dispatchers, Follow safety procedures for transporting dangerous goods, Read and interpret maps, Read written directions, Determine vehicle routes, Operate truck cab computers, Operate CB radios, Operate telephones, Operate GPS systems, Exchange information with dispatchers, Exchange information with supervisors, Exchange information with other drivers, Complete all paperwork, Turn in all documentation, Comply with company SIPS, Comply with EMS policies, Comply with BMS policies, Report environmental issues immediately, Understand emergency notification process, Review emergency notification policy", "teamCollaboration" : "Collaborate with drivers; Collaborate with dispatchers", "domainKnowledge" : "Transporting dangerous goods", "domainList" : [ "transporting-dangerous-goods" ], "domainSpecificKnowledge" : [ "Transporting dangerous goods" ], "toolProficiency" : [ "Truck cab computers", "CB radios", "Telephones", "GPS systems" ], "documentationSkills" : "Complete paperwork; Turn in documentation", "specialRequirements" : "Lift 50 pounds, Hook up trailer, Back under trailer, Raise landing gear, Hook up airlines, Roll up landing gear, Roll down landing gear, Operate manual transmission tractor, Climb into engine, Bend, Stoop, Crawl, Open trailer gates, Close trailer gates, Open trailer doors, Close trailer doors, Get in and out of cab, Move upper torso when backing, Lean out of window, Report problems on farm, Report problems at plant, Work nights, Work weekends, Work holidays", "qualificationsBasic" : "1 Year Minimum CDL Driving Experience, Valid Class A or Commercial Driver's License, Acceptable driving record, Meet DOT requirements, Pass background, drug screen, and physical, Highschool Diploma or GED", "qualificationsPreferred" : "Class A preferred", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**If you are currently employed at Smithfield, please log into Workday and submit your application through the Jobs Hub.** Have a seat at our table. When you join Smithfield, you become part of something special – a company that's sustainably feeding people around the world, producing good food the right way with respect for our people, animals, communities and planet. With opportunities across locations and functions, a culture grounded in our Core Four values - gratitude, communication, respect and accountability - and a strong commitment to learning, collaboration, and innovation, Smithfield offers challenging and rewarding careers where you can grow, contribute and make a real impact. **Apply Now!** **Your Opportunity** ** _Compensation $21.75 + PBL - EXPERIENCED CDL DRIVERS (1 yr or more exp)._** **_Nights/Full Time/ Benefits after 90 days._** **_Must have 1 year or more CDL Driving Experience + Good Driving Record!_** **_** LOCAL** Magnolia and surrounding areas._** **Responsible for driving ADU truck on a route-oriented basis to various farms, servicing ADU containers, and transporting product to a rendering facility to be offloaded.** **Core Responsibilities** • Complete assigned route in a safe and productive manner. Perform pre-trip and post trip inspections on vehicle to ensure that equipment is in good working condition. • Collaborate with other drivers and dispatchers to insure scheduling. • Follow appropriate safety procedures for transporting dangerous goods. • Read and interpret maps, and written directions to determine vehicle routes. Operate equipment, such as truck cab computers, CB radios, telephones and GPS systems, to exchange necessary information with dispatchers, supervisors, and other driver. • Complete and turn in all paperwork and related documentation upon completion of shift. • Incumbent will be responsible for understanding and complying with company SIPS, EMS and BMS policies and procedures while performing their job duties. • Report all environmental issues immediately to their supervisor. Read and understand the company’s emergency notification process and will be responsible for reviewing that policy at their work site. • Any other duties as assigned. _The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. May perform other duties as assigned._ **Qualifications** To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals to perform the essential functions. • Highschool Diploma or GED required. • 1 Year Minimum CDL Driving Experience. • Valid Class A or B Commercial Driver's License with acceptable driving record. Class A preferred • Meet DOT requirements. (Pass background, drug screen, and physical). Must have acceptable driving record. Must be able to work a flexible schedule (NIGHTS, WEEKENDS, & HOLIDAYS as required.) **Work Environment & Physical Demands** _The work environment characteristics & physical demands described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions._ * Must be able to lift 50 pounds. * Hook up trailer to tractor, this includes backing under the trailer, raising landing gear and hooking up airlines. * Roll up and down landing gear that can require use of two hands and upper torso when on ground and one when gear clears the ground. * Operate a manual transmission tractor * During pre-trip of equipment be able to climb into engine area; bend, stoop, and crawl to complete through pre-trip. * Open and close trailer gates and doors to load and unload animals. * Get in and out of cab in tight places such as fuel islands. * Move upper torso when backing may require leaning out of window to see blind spot and/or mirrors. * Report problems encountered on the farm or designated plant through the swine movement ticket or farm condition report. * Read and understand the Smithfield emergency notification process knowing how and who to contact in case of an emergency. IndSPR-Hog Relocation Package AvailableNo **EEO Information** _Smithfield is an equal opportunity employer committed to workplace diversity. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, age, gender identity, protected veterans status, status as a disabled individual or any other protected group status or non-job characteristic as directed by law._ _If you are an individual with a disability and would like to request a reasonable accommodation for any part of the employment selection process, please call us at 757-357-1595._", "summaryDescription" : "CDL A - Ag Protein (nights) at Smithfield. Skills: CDL Driving, Route operations. Drive ADU truck on route. Service ADU containers", "postedDate" : "2026-06-12T07:10:47.067", "createdAt" : "2026-06-12T07:10:47.037", "lastUpdated" : "2026-06-14T22:55:03.485", "ingestTimestamp" : "2026-06-12T07:10:47.037", "mongoId" : "6a2b2ebd74d8ee00a0785480", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://smithfieldfoods.wd1.myworkdayjobs.com/Careers/job/Magnolia-NC/ADU-CDL-Driver-Trainee_R-2026-7235", "salaryAnnualMin" : 45240, "salaryAnnualMax" : 45240, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Driving", "Route planning", "CDL Driving", "Route operations", "Transporting dangerous goods", "CDL A", "Truck cab computers", "CB radios", "Telephones", "GPS systems" ], "skillCount" : 10, "jobCategory" : "other", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true }, { "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" : "6a305a9cf292fd229cf5359b", "title" : "Cannabis Lab & Extraction Manager", "industry" : "Manufacturing", "salary" : { "min" : 85000.0, "max" : 125000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Manager in the Cannabis industry in Otsego, United States, adjusted for seniority and industry." }, "location" : "Otsego & Elk River, MN", "locations" : [ "Otsego & Elk River, MN" ], "timestamp" : "2026-06-16T07:27:27.511", "fingerprint" : "60c922a32d51a1179c627c9a8b221f432646d43bb7d02175736f9f0f01f674e1", "source" : "jazzhr", "language" : "en", "externalId" : "DlmVbZFC8p", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Otsego", "state" : "Minnesota", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "45.2812733,-93.6148570" }, { "city" : "Elk River", "state" : "Minnesota", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "45.3038538,-93.5671825" } ], "locationText" : "Otsego, Minnesota, United States; Elk River, Minnesota, United States", "experienceLevel" : "Manager", "workSiteFlexibility" : "Onsite", "summaryDescription" : "Cannabis Lab & Extraction Manager", "createdAt" : "2026-06-15T22:20:13.705", "lastUpdated" : "2026-06-16T07:27:27.511", "ingestTimestamp" : "2026-06-15T22:20:13.705", "mongoId" : "6a305a9cf292fd229cf5359b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 85000, "salaryAnnualMax" : 125000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Manager", "dataQualityScore" : 0.44444445, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Cannabis", "llmIndustryConfidence" : 0.9 }, { "id" : "6a305b92f292fd229cf5ef91", "title" : "Qualitätsbeauftragter in der Produktion rekombinanter Proteine (m|w|d)", "company" : "Miltenyi Biotec", "industry" : "Biotechnology", "salary" : { "min" : 58000.0, "max" : 78000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Mid-level Quality Officer in Biotec in Teterow, Germany, adjusted for company size and industry." }, "location" : "Teterow, Germany", "locations" : [ "Teterow", "Germany" ], "timestamp" : "2026-06-16T08:31:45.312", "fingerprint" : "4c12752f8967fc2d002135bdca1134b7fb8ebfcba9f9393be60fe30b4e60c512", "source" : "smartrecruiters", "language" : "de", "applyUrl" : "https://jobs.smartrecruiters.com/MiltenyiBiotec1/744000132153720-qualitatsbeauftragter-in-der-produktion-rekombinanter-proteine-m-w-d-", "externalId" : "744000132153720", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Teterow", "country" : "Germany", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "53.7709505,12.5753569" } ], "locationText" : "Teterow, Germany", "employmentType" : "FULL_TIME", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "mid", "professionalSkills" : [ "Qualitätsbewusstsein" ], "hardSkillsList" : [ "GMP-konforme Produktion", "Prozessrisikoanalysen", "Validierungspläne", "Qualifizierungsdokumente", "Validierungsdokumente" ], "hardSkills" : [ { "name" : "GMP-konforme Produktion", "level" : "intermediate" }, { "name" : "Prozessrisikoanalysen", "level" : "intermediate" }, { "name" : "Validierungspläne", "level" : "intermediate" }, { "name" : "Qualifizierungsdokumente", "level" : "intermediate" }, { "name" : "Validierungsdokumente", "level" : "intermediate" } ], "majorSkills" : "GMP-Compliance, Qualitätssicherung, Dokumentenmanagement", "majorSkillsList" : [ "GMP-Compliance", "Qualitätssicherung", "Dokumentenmanagement" ], "coreResponsibilities" : "Umsetzung und Einhaltung relevanter Vorschriften, Sicherstellung reproduzierbarer Ergebnisse, Sicherstellung der Produktqualität, Planung und Koordination interner Freigaben, Kontrolle der Chargendokumentation, Erstellung, Lenkung und Pflege GMP-Dokumentationen, Erstellung von Abweichungsberichten, Erstellung von Änderungsanträgen, Unterstützung bei Umsetzung von Maßnahmen, Unterstützung bei Erstellung von Risikoanalysen, Unterstützung bei Erstellung von Validierungsplänen, Unterstützung bei Erstellung von Qualifizierungsdokumenten, Unterstützung bei Erstellung von Validierungsdokumenten, Analyse und Verbesserung bestehender Prozesse, Umsetzung von Trainingsmaßnahmen", "teamCollaboration" : "Interdisziplinäre Teams; Zusammenarbeit mit Produktion; Zusammenarbeit mit Prozessentwicklung; Zusammenarbeit mit Qualitätskontrolle; Zusammenarbeit mit Qualitätssicherung; Zusammenarbeit mit Regulatory Affairs", "domainKnowledge" : "GMP-guideline; ISO 13485; Rekombinante Proteine; Therapeutische Zwecke; Zell- und Gentherapien", "domainList" : [ "gmp-guideline", "iso-13485", "rekombinante-proteine", "therapeutische-zwecke", "zell-und-gentherapien" ], "domainSpecificKnowledge" : [ "GMP-guideline", "ISO 13485", "Rekombinante Proteine", "Therapeutische Zwecke", "Zell- und Gentherapien" ], "toolProficiency" : [ "MS-Office" ], "documentationSkills" : "Chargendokumentation; GMP-Dokumentation; Abweichungsberichte; Änderungsanträge; Validierungspläne; Qualifizierungsdokumente; Validierungsdokumente", "continuousLearning" : "Individuelle Weiterbildung", "innovationCreativity" : "Entwicklung innovativer Therapien", "problemSolvingSkills" : "Lösungsorientiertes Denken", "qualificationsBasic" : "Masterstudium naturwissenschaftlich oder Qualitätswesen, Ausgeprägtes technisches Verständnis, Strukturiertes und gewissenhaftes Arbeiten, Konzeptionelles, lösungsorientiertes Denken, Zuverlässigkeit und Teamfähigkeit, Sicherer Umgang mit MS-Office-Programmen, Gute Deutschkenntnisse, Gute Englischkenntnisse", "qualificationsPreferred" : "Berufserfahrung im regulierten Umfeld", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Seit 35 Jahren entwickeln wir einzigartige Lösungen für die biomedizinische Spitzenforschung sowie für neuartige Zell- und Gentherapien. Wir tragen dazu bei, medizinische Methoden zu revolutionieren, um Krebs und andere schwere Krankheiten zu besiegen. Uns kennzeichnet ein Arbeitsumfeld, das von Kreativität und eigenverantwortlichem Arbeiten geprägt ist. Bei Miltenyi Biotec arbeiten mehr als 5.000 Menschen aus über 75 Ländern zusammen und bilden die Basis für unseren nachhaltigen Erfolg. An unserem Standort in Teterow – in der Nähe von Rostock – sind Sie in der Abteilung „Manufacturing Microbial Products - Quality“ beschäftigt. Sie sind Mitglied des Teams, welches die GMP-konforme Produktion rekombinanter Proteine für therapeutische Zwecke sicherstellt. Es erwartet Sie ein vielfältiges Aufgabenspektrum mit der Möglichkeit, an der Entwicklung und Realisierung innovativer Therapien zur Behandlung von Krebs und Autoimmunkrankheiten mitzuwirken. * In Ihrer Rolle sind Sie für die Umsetzung und Einhaltung der relevanten Vorschriften (GMP-guideline, ISO 13485) innerhalb der Abteilung verantwortlich. Sie stellen sicher, dass die Herstellprozesse über die gesamte Dauer des Produktlebenszyklus zu reproduzierbaren Ergebnissen führen und die Qualität der Produkte eingehalten wird. * Sie planen und koordinieren die interne Freigabe der unter GMP-Bedingungen produzierten Produkte. Die Kontrolle der Chargendokumentation auf Vollständigkeit und Richtigkeit stellt einen weiteren Schwerpunkt ihrer täglichen Arbeit dar. * Da Sie an der Herstellung von Produkten mit hohen regulatorischen Anforderungen beteiligt sind, stellen die Erstellung, Lenkung und Pflege relevanter GMP-Dokumentationen einen wichtigen Baustein Ihres Aufgabengebietes dar. * Darüber hinaus erstellen Sie Abweichungsberichte, Änderungsanträge und unterstützen bei der Umsetzung der entsprechenden Maßnahmen. * Sie unterstützen ihre Kollegen bei der Erstellung und Pflege von (Prozess-)Risikoanalysen, Validierungsplänen und Qualifizierungs-/Validierungsdokumenten. Die kontinuierliche Analyse und Verbesserung der bestehenden Prozesse stellen einen weiteren Aspekt ihrer Arbeit dar. * Sie verantworten die Umsetzung von Trainingsmaßnahmen im Team „Microbial Products“. Ferner agieren Sie in interdisziplinären Teams und arbeiten eng zusammen mit Kollegen aus Produktion, Prozessentwicklung, Qualitätskontrolle, Qualitätssicherung und Regulatory Affairs. ## Qualifications * Ihr Masterstudium im naturwissenschaftlichen Bereich oder im Qualitätswesen haben Sie erfolgreich abgeschlossen, und Sie verfügen über ein ausgeprägtes technisches Verständnis. * Idealerweise bringen Sie Berufserfahrung im regulierten Umfeld mit. * Sie überzeugen uns durch ihr stark ausgeprägtes Qualitätsbewusstsein. * Eine strukturierte und gewissenhafte Arbeitsweise sowie konzeptionelles, lösungsorientiertes Denken zeichnen Sie aus. Zuverlässigkeit und Teamfähigkeit sind für Sie selbstverständlich. * Ein sicherer Umgang mit MS-Office-Programmen sowie gute Deutsch- und Englischkenntnisse in Wort und Schrift runden Ihr Profil ab. ## Additional Information Was wir bieten * Arbeiten mit freier und selbstbestimmter Zeiteinteilung * Ein interkulturelles Umfeld, geprägt von Vielfalt, flachen Hierarchien, Duz-Kultur * Freiräume, um sich kreativ einzubringen und aktiv mitzugestalten * Individuelle Weiterbildung in unserer Miltenyi University als Kern der Miltenyi DNA * 30-Tage-Urlaub, vergünstigtes Deutschlandticket, (E)-Bike-Leasing, vermögenswirksame Leistungen, betriebliche Altersvorsorge, Berufsunfähigkeitsversicherung, Kantine u.v.m. Vielfalt ist die Grundlage unserer Kreativität bei Miltenyi Biotec. Bringen Sie sich ein, so wie Sie sind – unabhängig von Geschlecht, sexueller Identität, Alter, Herkunft, Religion oder Behinderung. Wir freuen uns auf Ihre Bewerbung Wenn Sie in einem offenen, kreativen und hilfsbereiten Team arbeiten möchten, bieten wir Ihnen hier das richtige Umfeld. Wir freuen uns auf Ihre Bewerbung – mit Ihrer Gehaltsvorstellung und Verfügbarkeit.", "summaryDescription" : "Qualitätsbeauftragter in der Produktion rekombinanter Proteine (m|w|d) at Miltenyi Biotec. Skills: GMP-Compliance, Qualitätssicherung, Dokumentenmanagement. Umsetzung und Einhaltung relevanter Vorschriften. Sicherstellung reproduzierbarer Ergebnisse", "postedDate" : "2026-06-15T09:39:09.000", "createdAt" : "2026-06-15T23:51:53.334", "lastUpdated" : "2026-06-16T08:31:45.312", "ingestTimestamp" : "2026-06-15T23:51:53.334", "mongoId" : "6a305b92f292fd229cf5ef91", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "50k-75k", "hasSalary" : false, "allSkills" : [ "GMP-konforme Produktion", "Prozessrisikoanalysen", "Validierungspläne", "Qualifizierungsdokumente", "Validierungsdokumente", "GMP-Compliance", "Qualitätssicherung", "Dokumentenmanagement", "Qualitätsbewusstsein", "GMP-guideline", "ISO 13485", "Rekombinante Proteine", "Therapeutische Zwecke", "Zell- und Gentherapien", "MS-Office" ], "skillCount" : 15, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a304fbdf292fd229cee9ab3", "title" : "Qualitätsbeauftragter in der Produktion rekombinanter Proteine (m|w|d)", "company" : "Miltenyi Biotec", "industry" : "Biotechnology", "salary" : { "min" : 58000.0, "max" : 78000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Mid-level Quality Officer in Biotec in Teterow, Germany, adjusted for company size and industry." }, "location" : "Teterow, Germany", "locations" : [ "Teterow", "Germany" ], "timestamp" : "2026-06-16T07:11:40.589", "fingerprint" : "f26cd0c332a19fffcb74edcee5a464635e1cab84df4dd8ace6791504253b9cac", "source" : "smartrecruiters", "language" : "de", "applyUrl" : "https://jobs.smartrecruiters.com/MiltenyiBiotec1/744000132153720-qualitatsbeauftragter-in-der-produktion-rekombinanter-proteine-m-w-d-", "externalId" : "744000132153720", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Teterow", "country" : "Germany", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "53.7709505,12.5753569" } ], "locationText" : "Teterow, Germany", "employmentType" : "FULL_TIME", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "mid", "professionalSkills" : [ "Qualitätsbewusstsein" ], "hardSkillsList" : [ "GMP-konforme Produktion", "Prozessrisikoanalysen", "Validierungspläne", "Qualifizierungsdokumente", "Validierungsdokumente" ], "hardSkills" : [ { "name" : "GMP-konforme Produktion", "level" : "intermediate" }, { "name" : "Prozessrisikoanalysen", "level" : "intermediate" }, { "name" : "Validierungspläne", "level" : "intermediate" }, { "name" : "Qualifizierungsdokumente", "level" : "intermediate" }, { "name" : "Validierungsdokumente", "level" : "intermediate" } ], "majorSkills" : "GMP-Compliance, Qualitätsdokumentation, Prozessverbesserung", "majorSkillsList" : [ "GMP-Compliance", "Qualitätsdokumentation", "Prozessverbesserung" ], "coreResponsibilities" : "Umsetzung und Einhaltung relevanter Vorschriften, Sicherstellung reproduzierbarer Ergebnisse, Sicherstellung der Produktqualität, Planung und Koordination interner Freigaben, Kontrolle der Chargendokumentation, Erstellung, Lenkung und Pflege relevanter GMP-Dokumentationen, Erstellung von Abweichungsberichten, Erstellung von Änderungsanträgen, Unterstützung bei Umsetzung von Maßnahmen, Unterstützung bei Erstellung von Risikoanalysen, Unterstützung bei Erstellung von Validierungsplänen, Unterstützung bei Erstellung von Qualifizierungsdokumenten, Unterstützung bei Erstellung von Validierungsdokumenten, Kontinuierliche Analyse bestehender Prozesse, Verbesserung bestehender Prozesse, Umsetzung von Trainingsmaßnahmen", "teamCollaboration" : "Interdisziplinäre Teams; Zusammenarbeit mit Produktion; Zusammenarbeit mit Prozessentwicklung; Zusammenarbeit mit Qualitätskontrolle; Zusammenarbeit mit Qualitätssicherung; Zusammenarbeit mit Regulatory Affairs", "domainKnowledge" : "GMP-guideline; ISO 13485; Rekombinante Proteine; Therapeutische Zwecke; Zell- und Gentherapien", "domainList" : [ "gmp-guideline", "iso-13485", "rekombinante-proteine", "therapeutische-zwecke", "zell-und-gentherapien" ], "domainSpecificKnowledge" : [ "GMP-guideline", "ISO 13485", "Rekombinante Proteine", "Therapeutische Zwecke", "Zell- und Gentherapien" ], "toolProficiency" : [ "MS-Office" ], "documentationSkills" : "GMP-Dokumentation; Chargendokumentation; Abweichungsberichte; Änderungsanträge; Validierungspläne; Qualifizierungsdokumente; Validierungsdokumente", "continuousLearning" : "Individuelle Weiterbildung", "innovationCreativity" : "Entwicklung innovativer Therapien", "problemSolvingSkills" : "Lösungsorientiertes Denken", "qualificationsBasic" : "Masterstudium naturwissenschaftlich oder Qualitätswesen, Ausgeprägtes technisches Verständnis, Strukturiertes und gewissenhaftes Arbeiten, Konzeptionelles, lösungsorientiertes Denken, Zuverlässigkeit und Teamfähigkeit, Sicherer Umgang mit MS-Office-Programmen, Gute Deutschkenntnisse, Gute Englischkenntnisse", "qualificationsPreferred" : "Berufserfahrung im regulierten Umfeld", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Seit 35 Jahren entwickeln wir einzigartige Lösungen für die biomedizinische Spitzenforschung sowie für neuartige Zell- und Gentherapien. Wir tragen dazu bei, medizinische Methoden zu revolutionieren, um Krebs und andere schwere Krankheiten zu besiegen. Uns kennzeichnet ein Arbeitsumfeld, das von Kreativität und eigenverantwortlichem Arbeiten geprägt ist. Bei Miltenyi Biotec arbeiten mehr als 5.000 Menschen aus über 75 Ländern zusammen und bilden die Basis für unseren nachhaltigen Erfolg. An unserem Standort in Teterow – in der Nähe von Rostock – sind Sie in der Abteilung „Manufacturing Microbial Products - Quality“ beschäftigt. Sie sind Mitglied des Teams, welches die GMP-konforme Produktion rekombinanter Proteine für therapeutische Zwecke sicherstellt. Es erwartet Sie ein vielfältiges Aufgabenspektrum mit der Möglichkeit, an der Entwicklung und Realisierung innovativer Therapien zur Behandlung von Krebs und Autoimmunkrankheiten mitzuwirken. * In Ihrer Rolle sind Sie für die Umsetzung und Einhaltung der relevanten Vorschriften (GMP-guideline, ISO 13485) innerhalb der Abteilung verantwortlich. Sie stellen sicher, dass die Herstellprozesse über die gesamte Dauer des Produktlebenszyklus zu reproduzierbaren Ergebnissen führen und die Qualität der Produkte eingehalten wird. * Sie planen und koordinieren die interne Freigabe der unter GMP-Bedingungen produzierten Produkte. Die Kontrolle der Chargendokumentation auf Vollständigkeit und Richtigkeit stellt einen weiteren Schwerpunkt ihrer täglichen Arbeit dar. * Da Sie an der Herstellung von Produkten mit hohen regulatorischen Anforderungen beteiligt sind, stellen die Erstellung, Lenkung und Pflege relevanter GMP-Dokumentationen einen wichtigen Baustein Ihres Aufgabengebietes dar. * Darüber hinaus erstellen Sie Abweichungsberichte, Änderungsanträge und unterstützen bei der Umsetzung der entsprechenden Maßnahmen. * Sie unterstützen ihre Kollegen bei der Erstellung und Pflege von (Prozess-)Risikoanalysen, Validierungsplänen und Qualifizierungs-/Validierungsdokumenten. Die kontinuierliche Analyse und Verbesserung der bestehenden Prozesse stellen einen weiteren Aspekt ihrer Arbeit dar. * Sie verantworten die Umsetzung von Trainingsmaßnahmen im Team „Microbial Products“. Ferner agieren Sie in interdisziplinären Teams und arbeiten eng zusammen mit Kollegen aus Produktion, Prozessentwicklung, Qualitätskontrolle, Qualitätssicherung und Regulatory Affairs. ## Qualifications * Ihr Masterstudium im naturwissenschaftlichen Bereich oder im Qualitätswesen haben Sie erfolgreich abgeschlossen, und Sie verfügen über ein ausgeprägtes technisches Verständnis. * Idealerweise bringen Sie Berufserfahrung im regulierten Umfeld mit. * Sie überzeugen uns durch ihr stark ausgeprägtes Qualitätsbewusstsein. * Eine strukturierte und gewissenhafte Arbeitsweise sowie konzeptionelles, lösungsorientiertes Denken zeichnen Sie aus. Zuverlässigkeit und Teamfähigkeit sind für Sie selbstverständlich. * Ein sicherer Umgang mit MS-Office-Programmen sowie gute Deutsch- und Englischkenntnisse in Wort und Schrift runden Ihr Profil ab. ## Additional Information Was wir bieten * Arbeiten mit freier und selbstbestimmter Zeiteinteilung * Ein interkulturelles Umfeld, geprägt von Vielfalt, flachen Hierarchien, Duz-Kultur * Freiräume, um sich kreativ einzubringen und aktiv mitzugestalten * Individuelle Weiterbildung in unserer Miltenyi University als Kern der Miltenyi DNA * 30-Tage-Urlaub, vergünstigtes Deutschlandticket, (E)-Bike-Leasing, vermögenswirksame Leistungen, betriebliche Altersvorsorge, Berufsunfähigkeitsversicherung, Kantine u.v.m. Vielfalt ist die Grundlage unserer Kreativität bei Miltenyi Biotec. Bringen Sie sich ein, so wie Sie sind – unabhängig von Geschlecht, sexueller Identität, Alter, Herkunft, Religion oder Behinderung. Wir freuen uns auf Ihre Bewerbung Wenn Sie in einem offenen, kreativen und hilfsbereiten Team arbeiten möchten, bieten wir Ihnen hier das richtige Umfeld. Wir freuen uns auf Ihre Bewerbung – mit Ihrer Gehaltsvorstellung und Verfügbarkeit.", "summaryDescription" : "Qualitätsbeauftragter in der Produktion rekombinanter Proteine (m|w|d) at Miltenyi Biotec. Skills: GMP-Compliance, Qualitätsdokumentation, Prozessverbesserung. Umsetzung und Einhaltung relevanter Vorschriften. Sicherstellung reproduzierbarer Ergebnisse", "postedDate" : "2026-06-15T09:39:09.000", "createdAt" : "2026-06-15T21:46:24.940", "lastUpdated" : "2026-06-16T07:11:40.589", "ingestTimestamp" : "2026-06-15T21:46:24.940", "mongoId" : "6a304fbdf292fd229cee9ab3", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "50k-75k", "hasSalary" : false, "allSkills" : [ "GMP-konforme Produktion", "Prozessrisikoanalysen", "Validierungspläne", "Qualifizierungsdokumente", "Validierungsdokumente", "GMP-Compliance", "Qualitätsdokumentation", "Prozessverbesserung", "Qualitätsbewusstsein", "GMP-guideline", "ISO 13485", "Rekombinante Proteine", "Therapeutische Zwecke", "Zell- und Gentherapien", "MS-Office" ], "skillCount" : 15, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ca57f74d8ee00a09b6d71", "title" : "Co-Op, Data Extraction", "company" : "Lila Sciences", "industry" : "Technology", "salary" : { "min" : 48000.0, "max" : 65000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level Data Extraction Co-Op in Cambridge, United States, adjusted for the biotech industry and internship employment type." }, "location" : "Alewife, Cambridge, MA", "locations" : [ "Alewife", "Cambridge", "MA" ], "timestamp" : "2026-06-16T03:08:10.298", "fingerprint" : "d6889434017c55cb43df95347afff24f2fdb81c2ec8fab0818fd2b42e84b8bd2", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/lilasciences/jobs/4280811009", "externalId" : "4280811009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Cambridge", "state" : "Massachusetts", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.3656347,-71.1040018" } ], "locationText" : "Cambridge, Massachusetts, United States", "employmentType" : "INTERNSHIP", "technicalSkills" : "Python, NLP, Computer vision, Machine learning", "hardSkillsList" : [ "Data extraction", "Model evaluation", "Pipeline building", "Data structuring" ], "hardSkills" : [ { "name" : "Data extraction", "level" : "intermediate" }, { "name" : "Model evaluation", "level" : "intermediate" }, { "name" : "Pipeline building", "level" : "intermediate" }, { "name" : "Data structuring", "level" : "intermediate" } ], "majorSkills" : "Data extraction, Machine learning, NLP, Computer vision", "majorSkillsList" : [ "Data extraction", "Machine learning", "NLP", "Computer vision" ], "coreResponsibilities" : "Contribute to AI systems, Extract and structure knowledge, Fine-tune models, Evaluate models, Build pipelines, Test pipelines, Structure unstructured scientific data, Run extraction pipelines, Analyze results, Document findings, Share work through presentation, Write-up work, Contribute to publication, Contribute to open-source project", "teamCollaboration" : "Alongside research scientists; Alongside engineers", "domainKnowledge" : "Scientific literature; Scientific patents; Scientific data; Scientific document parsing", "domainList" : [ "scientific-literature", "scientific-patents", "scientific-data", "scientific-document-parsing" ], "domainSpecificKnowledge" : [ "Scientific literature", "Scientific patents", "Scientific data", "Scientific document parsing" ], "communicationSkills" : "Document findings clearly; Share work", "documentationSkills" : "Document findings", "continuousLearning" : "Willingness to learn quickly", "qualificationsBasic" : "Bachelor's, Master's, or PhD in Computer Science, Chemistry, Materials Science, or related field, Solid foundation in machine learning fundamentals, Python proficiency", "qualificationsPreferred" : "Coursework or projects involving multimodal models, Coursework or projects involving document understanding, Experience working with messy, real-world datasets, Interest in scientific document parsing", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Your Impact at LILA Lila Sciences builds AI systems that accelerate discovery across the physical and life sciences. Within Physical Sciences AI, our team works on turning unstructured scientific knowledge (e.g., literature, patents, technical reports) into structured signals that power downstream Lila applications. As a Data Extraction Co-Op, you will work alongside research scientists and engineers on a focused sub-problem in this stack. You will get hands-on experience fine-tuning and evaluating extraction models, building pipelines for messy real-world data, and shipping work that flows into production systems. What You'll Be Building Contribute to AI systems that extract and structure knowledge from scientific literature and patents, focused on a well-defined sub-problem Fine-tune and evaluate language, multimodal, or specialized models for data extraction, with mentor guidance Build and test pipelines that structure unstructured scientific data across text, tables, and visuals Run extraction pipelines, analyze results, and document findings clearly Share your work through a team presentation, write-up, or contribution to a publication or open-source project What You'll Need to Succeed Pursuing a Bachelor's, Master's, or PhD in Computer Science, Chemistry, Materials Science, or a related field Solid foundation in machine learning fundamentals and Python Familiarity with NLP or computer vision concepts Curiosity about scientific data and willingness to learn quickly in a research setting Bonus Points For Coursework or projects involving multimodal models or document understanding (OCR, table/figure extraction) Experience working with messy, real-world datasets Interest in scientific document parsing About LILA Lila Sciences is building Scientific Superintelligence™ to solve humankind's greatest challenges. We believe science is the most inspiring frontier for AI. Rather than hard-coding expert knowledge into tools, LILA builds systems that can learn for themselves. LILA combines advanced AI models with proprietary AI Science Factory™ instruments into an operating system for science that executes the entire scientific method autonomously, accelerating discovery at unprecedented speed, scale, and impact across medicine, materials, and energy. Learn more at www.lila.ai. Guided by our core values of truth, trust, curiosity, grit, and velocity, we move with startup speed while tackling problems of historic importance. If this sounds like an environment you'd love to work in, even if you don't meet every qualification listed above, we encourage you to apply. We’re All In Lila Sciences is committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. Information you provide during your application process will be handled in accordance with our Candidate Privacy Policy. A Note to Agencies Lila Sciences does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Lila Sciences or its employees is strictly prohibited unless contacted directly by Lila Science’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Lila Sciences, and Lila Sciences will not owe any referral or other fees with respect thereto.", "summaryDescription" : "Co-Op, Data Extraction at Lila Sciences. Skills: Data extraction, Machine learning, NLP, Computer vision. Contribute to AI systems. Extract and structure knowledge", "postedDate" : "2026-06-14T19:19:12.422", "createdAt" : "2026-06-14T19:19:12.422", "lastUpdated" : "2026-06-16T03:08:10.298", "ingestTimestamp" : "2026-06-14T19:19:12.422", "mongoId" : "6a2ca57f74d8ee00a09b6d71", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 48000, "salaryAnnualMax" : 65000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Data extraction", "Model evaluation", "Pipeline building", "Data structuring", "Machine learning", "NLP", "Computer vision", "Scientific literature", "Scientific patents", "Scientific data", "Scientific document parsing" ], "skillCount" : 11, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Entry", "dataQualityScore" : 0.8888889, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a307ca6f292fd229c04a87c", "title" : "Research Scientist, Proteins", "company" : "Louis Dreyfus Company", "industry" : "International Trade And Development", "salary" : { "min" : 135000.0, "max" : 195000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Senior Research Scientist in the Food & Beverage industry in Livermore, United States, adjusted for seniority and company size." }, "location" : "Livermore, CA, United States", "locations" : [ "Livermore", "CA", "United States" ], "timestamp" : "2026-06-16T12:10:30.062", "fingerprint" : "64f4735f90583ef2be3204bec1bf9c72038b83f4cce2f45bbe84be7cb1762b01", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/LouisDreyfusCompany/744000131764339-research-scientist-proteins", "externalId" : "744000131764339", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Livermore", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "37.6820583,-121.7680530" } ], "locationText" : "Livermore, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "PhD", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "mid", "technicalSkills" : "Protein Engineering, Antibody Engineering, Antibody Discovery, Antibody Development, Protein Expression, Protein Purification, Protein Characterization, Mammalian Cell Culture, Transient Transfection, Stable Cell Line, Protein Formulation, Protein Analytics, Biologics Development, CMC, Regulatory Filings", "professionalSkills" : [ "Project management", "Data analysis", "Experimental design" ], "hardSkillsList" : [ "Protein engineering", "Antibody engineering", "Antibody discovery", "Antibody development", "Protein expression", "Protein purification", "Protein characterization", "Mammalian cell culture", "Transient transfection", "Protein formulation", "Protein analytics", "Biologics development", "CMC", "Regulatory filings" ], "hardSkills" : [ { "name" : "Protein engineering", "level" : "intermediate" }, { "name" : "Antibody engineering", "level" : "intermediate" }, { "name" : "Antibody discovery", "level" : "intermediate" }, { "name" : "Antibody development", "level" : "intermediate" }, { "name" : "Protein expression", "level" : "intermediate" }, { "name" : "Protein purification", "level" : "intermediate" }, { "name" : "Protein characterization", "level" : "intermediate" }, { "name" : "Mammalian cell culture", "level" : "intermediate" }, { "name" : "Transient transfection", "level" : "intermediate" }, { "name" : "Protein formulation", "level" : "intermediate" }, { "name" : "Protein analytics", "level" : "intermediate" }, { "name" : "Biologics development", "level" : "intermediate" }, { "name" : "CMC", "level" : "intermediate" }, { "name" : "Regulatory filings", "level" : "intermediate" } ], "majorSkills" : "Protein Engineering, Antibody Engineering, Antibody Discovery, Antibody Development", "majorSkillsList" : [ "Protein Engineering", "Antibody Engineering", "Antibody Discovery", "Antibody Development" ], "coreResponsibilities" : "Design novel antibodies, Develop antibody engineering strategies, Optimize antibody expression, Purify antibodies, Characterize antibodies, Develop antibody discovery and development processes, Collaborate with cross-functional teams, Troubleshoot experimental issues, Document experimental results, Present findings to stakeholders", "teamCollaboration" : "Cross-functional teams; Stakeholders", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Antibody engineering; Antibody discovery; Antibody development; Biologics development; CMC; Regulatory filings", "domainList" : [ "antibody-engineering", "antibody-discovery", "antibody-development", "biologics-development", "cmc", "regulatory-filings" ], "domainSpecificKnowledge" : [ "Antibody engineering", "Antibody discovery", "Antibody development", "Biologics development", "CMC", "Regulatory filings" ], "communicationSkills" : "Present findings", "documentationSkills" : "Document experimental results", "problemSolvingSkills" : "Troubleshoot experimental issues", "qualificationsBasic" : "PhD in Protein Engineering, 5+ years of experience in protein engineering, Experience with protein expression, Experience with protein purification, Experience with protein characterization, Experience with antibody engineering, Experience with antibody discovery, Experience with antibody development", "qualificationsPreferred" : "Experience with mammalian cell culture, Experience with transient transfection, Experience with stable cell line development, Experience with protein formulation, Experience with protein analytics, Experience with biologics development, Experience with CMC, Experience with regulatory filings", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Louis Dreyfus Company is a leading merchant and processor of agricultural goods. Our activities span the entire value chain from farm to fork, across a broad range of business lines, we leverage our global reach and extensive asset network to serve our customers and consumers around the world. Structured as a matrix organization of six geographical regions and ten platforms, Louis Dreyfus Company is active in over 100 countries and employs approximately 18,000 people globally. Primary Responsibilities/Essential Functions * Plan, manage, execute protein extraction research from bench to pilot scale with goal of improving protein functionality with model food and beverage systems * Generate ideas and convert them into successful experiments with the goal to generate them into intellectual property * Actively collaborate with product development, process engineering, and analytics * Bottom-up innovative methods for the design of plant protein isolation, purification and characterization process that will be future ingredients in MRS for our customers * Data visualization and statistical analysis of experimental results as well as interpreting and communicating the findings of R&D team to the business unit * Serve as a subject matter expert in plant protein research that can mentor and help develop internal talent * Apply learning from patent landscape and public research to short, mid and long term in-house and external partner collaborative projects Additional Responsibilities Functions * Other duties as assigned by management. ## Qualifications Experience Basic qualification: * Knowledge of protein structure and function properties, polysaccharides, and fats within complex food matrix systems such as hydrocolloids, emulsions, foams, gels, etc. * Application of enzymes and chemicals for proteins, oils, and polysaccharide modifications. * Understanding of QA/QC, microbial safety, and sensory properties of proteins and food products. * Know-how in methods to characterize plant proteins and its use thereof in food and beverage systems using analytical methods such as rheology, texture analysis, particle size, scanning electron microscopy, proteomics, CD/DSC, SDS-PAGE etc., * Broad view on plant-based food and beverage industry and markets, in-depth knowledge on products. Education/Professional Certifications/Licenses * Ph. D in food science, protein chemistry, biochemistry, chemical engineering, chemistry, biology, or a related field. * Alternatively, a master’s degree in the above fields, with 5+ years of relevant food industry experience, or a bachelors with 10+ years of relevant food industry experience. Knowledge/Skills/Abilities (including any physical demands) Basic qualifications: * This position is a safety sensitive position and is subject to random drug testing. * Ability to sit, stand and walk for extended periods of time. * Ability to climb stairs and ladders as well as work at heights; * Ability to work in confined spaces. * Ability to work in a variety of temperatures and potential inclement weather. * Ability to withstand extended periods of walking and standing. * Ability to move manufacturing materials, products and equipment of 50 pounds or more, which requires bending and lifting. * Ability to wear Personal Protective Equipment (PPE) as is compliant with policies and procedures. * Ability to work in fast-paced lab environments. * Excellent verbal and written communication skills. * Proficiency with spreadsheet and word-processing software (e.g., Excel, Word, PowerPoint). * Strong analytical and problem-solving skills. * Ability to prioritize multiple tasks to meet strict monthly deadlines. * Proactively approaches job duties and potential problems. * Detail oriented with strong organizational and documentation skills. ## Additional Information Safety, Health and Environmental Requirements * This position is a safety sensitive position and is subject to random drug testing. * Ability to sit, stand and walk for extended periods of time. * Ability to move manufacturing materials, products and equipment of 50 pounds or more, which requires bending and lifting. * Ability to wear Personal Protective Equipment (PPE) as is compliant with policies and procedures. Working Conditions * Time split between pilot plant, office and lab environments. There may be extended periods of sitting or standing at a computer screen or counter. * Interacts closely with personnel in other departments and Company locations. * Interacts closely with middle and senior management personnel. * Extensions of regular working hours are occasionally necessary to complete time-sensitive projects or to respond to emergencies. Employee Supervision * Based upon business needs, may supervise 1 or 2 Research Assistants. Decision Making/Accountability * Handle and report issues or questions as directed by Livermore facility Management. Prioritizes personal workload throughout the day to ensure meeting of deadlines. What We Offer We provide a dynamic and stimulating international environment, which will stretch and develop your abilities and channel your skills and expertise with outstanding career development opportunities in one of the largest and most solid private companies in the world. - Comprehensive benefits program including medical, dental and vision care coverage, flexible spending account plans, employee assistance program, life insurance and disability coverage - 401k with Company Match - Family Friendly Benefits including childbirth and parental leave, fertility and family building benefits - Paid Time Off (PTO) and Paid Holidays - Flexible work available (not applicable to all roles) Diversity & Inclusion LDC is driven by a set of shared values and high ethical standards, with diversity and inclusion being part of our DNA. LDC is an equal opportunity employer committed to providing a working environment that embraces and values diversity, equity and inclusion. LDC encourages diversity, supports local communities and environmental initiatives. We encourage people of all backgrounds to apply. Equal employment opportunity (EEO) Louis Dreyfus Company provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Sustainability Sustainable value is at the heart of our purpose as a company. We are passionate about creating fair and sustainable value, both for our business and for other value chain stakeholders: our people, our business partners, the communities we touch and the environment around us", "summaryDescription" : "Research Scientist, Proteins at Louis Dreyfus Company. Skills: Protein Engineering, Antibody Engineering, Antibody Discovery, Antibody Development. Design novel antibodies. Develop antibody engineering strategies", "postedDate" : "2026-06-11T22:09:17.000", "createdAt" : "2026-06-16T01:35:45.143", "lastUpdated" : "2026-06-16T12:10:30.062", "ingestTimestamp" : "2026-06-16T01:35:45.143", "mongoId" : "6a307ca6f292fd229c04a87c", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 135000, "salaryAnnualMax" : 195000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Protein engineering", "Antibody engineering", "Antibody discovery", "Antibody development", "Protein expression", "Protein purification", "Protein characterization", "Mammalian cell culture", "Transient transfection", "Protein formulation", "Protein analytics", "Biologics development", "CMC", "Regulatory filings", "Protein Engineering", "Antibody Engineering", "Antibody Discovery", "Antibody Development", "Project management", "Data analysis", "Experimental design" ], "skillCount" : 21, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 1.0, "daysOld" : 4, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Food & Beverage", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2a830a74d8ee00a06750e5", "title" : "Associate Principal / Principal Scientist (Protein Science)", "company" : "GenScript/ProBio", "industry" : "Biotechnology", "salary" : { "min" : 150000.0, "max" : 250000.0, "currency" : "SGD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Lead Senior Scientist in Biotech in Singapore, adjusted for company size and experience level." }, "location" : "Singapore", "locations" : [ "Singapore" ], "timestamp" : "2026-06-14T21:07:17.797", "fingerprint" : "54075c582deb9ed6c37fb7a1067f2adfb53aa8ddb1057b9dcb8ed7c4c8ba92e5", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/genscript/jobs/5160645007", "externalId" : "5160645007", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Singapore", "country" : "Singapore", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "1.2899175,103.8519072" } ], "locationText" : "Singapore, Singapore", "experienceMinYears" : 10, "experienceMaxYears" : 99, "experienceLevel" : "Principal", "technicalSkills" : "Protein science, Molecular engineering, Biologics development, Structure prediction, Computational tools", "professionalSkills" : [ "Functional leadership", "Platform building", "Client-facing projects", "Tech transfer", "Operational deployment", "Intellectual property" ], "hardSkillsList" : [ "Antibody design", "Protein expression", "Protein purification", "Bispecific design", "Protein engineering", "Biophysical characterization", "Protein-protein interactions", "Analytical techniques", "SPR", "Mass spectrometry" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "Antibody design", "level" : "intermediate" }, { "name" : "Protein expression", "level" : "intermediate" }, { "name" : "Protein purification", "level" : "intermediate" }, { "name" : "Bispecific design", "level" : "intermediate" }, { "name" : "Protein engineering", "level" : "intermediate" }, { "name" : "Biophysical characterization", "level" : "intermediate" }, { "name" : "Protein-protein interactions", "level" : "intermediate" }, { "name" : "Analytical techniques", "level" : "intermediate" }, { "name" : "SPR", "level" : "intermediate" }, { "name" : "Mass spectrometry", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Bispecific Antibody Design, Protein Science, Molecular Engineering", "majorSkillsList" : [ "Bispecific Antibody Design", "Protein Science", "Molecular Engineering" ], "coreResponsibilities" : "Develop innovative strategies for design and engineering of, Implement innovative strategies for design and engineering of, Troubleshoot innovative strategies for design and engineering of, Design a portfolio of projects, Manage a portfolio of projects, Provide data-driven, structure-function insights, Improve expression, stability, and manufacturability, Oversee a team of research associates, Oversee a team of biotechnologists, Provide technical guidance to team, Foster a culture of excellence in protein science, Collaborate with cross-functional teams, Collaborate with cross-cultural teams, Support the development of biologics, Evaluate new technologies, Translate new technologies into production-ready solutions, Review advancements in antibody formats, Review advancements in engineering strategies, Review advancements in upstream and downstream integration impacts, Assess readiness of new technologies for tech transfer, Assess fit-for-purpose application across different molecule classes, Assess scalability and reproducibility, Assess impact on quality attributes, Act as a scientific bridge between R&D and, Ensure new platforms are scientifically sound, Ensure new platforms are translatable to production workflows, Ensure design decisions align with manufacturing realities, Partner with internal stakeholders, Develop design-for-manufacturability strategies, Develop internal guidelines for manufacturability, Develop AI-assisted design-for-manufacturability frameworks, Integrate AI-assisted design-for-manufacturability frameworks, Leverage internal datasets, Leverage external computational tools, Proactively identify risks, Proactively mitigate risks, Lead AI-enabled design initiatives, Support AI-enabled design initiatives, Translate computational design outputs into experimentally validated constructs, Ensure alignment between in silico design predictions and, Generate novel ideas, Contribute to intellectual property portfolio, Draft scientific papers, File patents, Report innovations in scientific forums, Contribute to development of scientific publications, Contribute to conference presentations, Contribute to webinars, Prepare technical reports, Review technical reports, Prepare technical documentation, Review technical documentation", "teamCollaboration" : "Cross-functional teams; Cross-cultural teams; Internal stakeholders; Quality Assurance; Process Development; Manufacturing", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Antibody formats; Protein science; Biologics production; Molecular engineering; Structure prediction; Developability scoring; Aggregation; Mispairing; Heterogeneity", "domainList" : [ "antibody-formats", "protein-science", "biologics-production", "molecular-engineering", "structure-prediction", "developability-scoring", "aggregation", "mispairing", "heterogeneity" ], "domainSpecificKnowledge" : [ "Antibody formats", "Protein science", "Biologics production", "Molecular engineering", "Structure prediction", "Developability scoring", "Aggregation", "Mispairing", "Heterogeneity" ], "toolProficiency" : [ "Computational tools" ], "communicationSkills" : "Scientific publications; Conference presentations; Webinars; Technical reports; Technical documentation", "documentationSkills" : "Technical documentation", "innovationCreativity" : "Innovation; Intellectual property; Novel ideas; R&D innovation", "problemSolvingSkills" : "Problem-solving skills; Troubleshooting", "qualificationsBasic" : "Ph.D. in Biochemistry, Molecular Biology, Cell Biology, Structural Biology, Bioengineering or related field, At least 5 years of experience in antibody design, protein expression, and purification, Expertise in bispecific design, Troubleshooting expression challenges, Demonstrated record of success with protein engineering for enhanced protein expression or properties, Experience with biophysical characterization of proteins, Experience with assessment of protein-protein interactions, Analytical and problem-solving skills, Wide ranging experience in analytical techniques, Excellent written and verbal English communication skills", "qualificationsPreferred" : "Experience in an industrial setting, Familiarity with automation and high-throughput techniques for protein expression and purification", "workSiteFlexibility" : "Onsite", "rawDescription" : "About GenScript GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology. Position Overview: We are seeking a highly motivated and experienced Principal Scientist in Bispecific Antibody Design & Engineering to establish and strengthen Singapore’s role as a center of excellence for complex antibody design and molecular engineering. In this role, you will serve as a functional leader in molecular design, format selection and recommendation, and engineering strategy while enabling improved expression, developability, and manufacturability. Additionally, you will play a key role in client-facing projects, ensuring seamless collaboration and delivery of high-quality biologics solutions. This position requires a blend of platform building, leadership skills, and the ability to build cross effectively. Key Responsibilities: Biologics Production Leadership: Develop, triage, implement, and troubleshoot innovative strategies for the design and engineering of complex antibody formats (bispecifics, multivalent, Fc-fusions, VHH). to achieve high yields, purity, and functionality. Design and manage a portfolio of projects to provide data-driven, structure-function insights to improve expression, stability, and manufacturability. Oversee a team of research associates and/or biotechnologists, providing technical guidance and fostering a culture of excellence in protein science methodologies. Cross-Functional Collaboration: Collaborate with cross-functional and cross-cultural teams to support the development of biologics, with a focus on evaluate and translate new technologies into production-ready solutions. Periodically review internal and external advancements in: Antibody formats and engineering strategies Upstream and downstream integration impacts driven by molecule design Assess readiness of new technologies for tech transfer, including: Fit-for-purpose application across different molecule classes Scalability and reproducibility Impact on quality attributes (aggregation, mispairing, heterogeneity) Act as a scientific bridge between R&D innovation and operational deployment, ensuring: New platforms are not only scientifically sound but also translatable to production workflows Design decisions are aligned with manufacturing realities Partner with internal stakeholders (e.g., Quality Assurance, Process Development, and Manufacturing) to ensure alignment and efficiency in biologics production workflows. Develop design-for-manufacturability strategies and internal guidelines: Develop and integrate AI-assisted design-for-manufacturability frameworks, leveraging internal datasets and external computational tools (e.g., structure prediction, developability scoring) to proactively identify and mitigate risks such as aggregation, mispairing, and low expression in complex antibody formats. Lead or support AI-enabled design and innovation initiatives (internal and external partnerships, including governmental or consortium projects) by translating computational design outputs into experimentally validated constructs, and ensuring alignment between in silico design predictions and real-world expression, quality, and manufacturability outcomes. Innovation & Intellectual Property: Generate novel ideas and contribute to the company’s intellectual property portfolio by drafting scientific papers, filing patents and reporting innovations in scientific forums. Contribute to the development of scientific publications, conference presentations, and webinars to showcase innovative findings and advancements. Prepare and review technical reports and documentation to internal and external stakeholders. Qualifications and Preferred Skills: Ph.D., in Biochemistry, Molecular Biology, Cell Biology, Structural Biology, Bioengineering or a related field. At least 5 years of experience in antibody design, protein expression, and purification, preferably in an industrial setting. Strong expertise in bispecific design and troubleshooting expression challenges. A demonstrated record of success with protein engineering for enhanced protein expression or properties. Experience with the biophysical characterization of proteins and the assessment of protein-protein interactions. Familiarity with automation and high-throughput techniques for protein expression and purification. Strong analytical and problem-solving skills, with a wide ranging experience in analytical techniques such as SPR, and mass spectrometry. Excellent written and verbal English communication skills, with a track record of scientific publications, presentations, and conferences. GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.", "summaryDescription" : "Associate Principal / Principal Scientist (Protein Science) at GenScript/ProBio. Skills: Bispecific Antibody Design, Protein Science, Molecular Engineering. Develop innovative strategies for design and engineering of. Implement innovative strategies for design and engineering of", "postedDate" : "2026-06-11T22:09:12.938", "createdAt" : "2026-06-11T22:09:12.938", "lastUpdated" : "2026-06-14T21:07:17.797", "ingestTimestamp" : "2026-06-11T22:09:12.938", "mongoId" : "6a2a830a74d8ee00a06750e5", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "150k-200k", "hasSalary" : false, "allSkills" : [ "Antibody design", "Protein expression", "Protein purification", "Bispecific design", "Protein engineering", "Biophysical characterization", "Protein-protein interactions", "Analytical techniques", "SPR", "Mass spectrometry", "Leadership", "Mentoring", "Bispecific Antibody Design", "Protein Science", "Molecular Engineering", "Functional leadership", "Platform building", "Client-facing projects", "Tech transfer", "Operational deployment", "Intellectual property", "Project management", "Antibody formats", "Protein science", "Biologics production", "Molecular engineering", "Structure prediction", "Developability scoring", "Aggregation", "Mispairing", "Heterogeneity", "Computational tools" ], "skillCount" : 32, "jobCategory" : "other", "jobSubcategory" : "protein-&-antibody", "dataQualityScore" : 0.8888889, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotechnology" }, { "id" : "6a2a48eb74d8ee00a05e29a2", "title" : "Sales and Application Scientist – Protein Engineering (Non-Bench)", "company" : "Integral Molecular", "industry" : "Biotech", "salary" : { "min" : 95000.0, "max" : 135000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-seniority Sales and Application Scientist in the Biotech industry in Philadelphia, United States, adjusted for company size and specific role focus." }, "location" : "Philadelphia, Pennsylvania, United States", "locations" : [ "Philadelphia", "Pennsylvania", "United States" ], "timestamp" : "2026-06-14T22:15:12.063", "fingerprint" : "0f19bce5b303bbf3f38ed838a85e4826ba953bf229075d556afedc1f73b1ac1b", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/integralmolecular/jobs/5250576008", "externalId" : "5250576008", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Philadelphia", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "39.9527237,-75.1635262" } ], "locationText" : "Philadelphia, Pennsylvania, United States", "minimumEducation" : "PhD", "professionalSkills" : [ "Commercial development", "Revenue targets", "Pipeline forecasting", "Opportunity tracking", "Market intelligence" ], "hardSkillsList" : [ "Technical feasibility", "Risk assessment" ], "hardSkills" : [ { "name" : "Technical feasibility", "level" : "intermediate" }, { "name" : "Risk assessment", "level" : "intermediate" } ], "majorSkills" : "Protein Engineering, Sales, Application Science", "majorSkillsList" : [ "Protein Engineering", "Sales", "Application Science" ], "coreResponsibilities" : "Prospect and convert accounts, Vet technical feasibility, Vet risk, Partner with product manager, Set revenue targets, Own attainment of targets, Serve as technical SME, Run calls independently, Manage active customer projects, Provide status updates, Manage timeline, Coordinate deliverables, QC reports, Co-deliver customer data reports, Ensure scientific accuracy, Ensure outputs on-scope, Own CRM hygiene, Own pipeline forecasting, Own opportunity tracking, Contribute commercial forecast, Represent Integral Molecular externally, Bring market intelligence back", "teamCollaboration" : "Scientific team; Product manager; Scientific leaders; Product leaders", "projectManagementSkills" : [ "Timeline management" ], "domainKnowledge" : "Protein Engineering platform; Biotech; Pharma; Therapeutics", "domainList" : [ "protein-engineering-platform", "biotech", "pharma", "therapeutics" ], "domainSpecificKnowledge" : [ "Protein Engineering platform", "Biotech", "Pharma", "Therapeutics" ], "toolProficiency" : [ "CRM" ], "communicationSkills" : "Presenting science; Business conversations", "problemSolvingSkills" : "Vetting technical feasibility; Vetting risk", "outcomesObjectives" : "Own attainment of revenue targets", "qualificationsBasic" : "PhD in biological sciences, Life sciences commercial experience", "qualificationsPreferred" : "Experience closing deals, Proven ability to prospect, Manage a pipeline, Close sales, Scientific storyteller, Comfortable presenting science", "remoteFriendly" : false, "workSiteFlexibility" : "Flexible", "rawDescription" : "Sales and Application Scientist - Protein Engineering (Non-Bench) - Job ID # 06032026 Are you a scientist who can walk into a room of discovery researchers or IP attorneys and earn their trust? Do you have experience closing deals for a commercial product? Join Integral Molecular as a Sales and Application Scientist where you will own commercial development for our Protein Engineering (PE) platform, independently prospecting, closing, and delivering customer projects. If you are eager to make a difference and be part of an organization that encourages your enterprising spirit, we welcome you to join our team. We are proud of our inclusive company culture where every individual is valued and feels a sense of belonging. Take the next step in your career path with us. What you will gain from working at Integral Molecular: Build something. You are commercializing the PE platform in an open market; building the territory from the ground up, not inheriting one Stay scientific. Exposure to cutting-edge therapeutics and platforms from across the biotech and pharma ecosystem, without the bench Stability and momentum. With 25 years of independent ownership, we have the freedom to continuously innovate A company culture and a city you’ll enjoy. Work in the heart of Philadelphia’s biotech hub with a flexible schedule, supportive culture, and leaders committed to your growth What you will do at Integral Molecular Prospect and convert biotech, pharma, and IP accounts through outbound outreach and conferences, vetting technical feasibility and risk with the scientific team first. Partner with the product manager to set revenue targets by market and customer persona, and own attainment of those targets. Serve as the technical SME on all pre- and post-sale customer discussions; master the PE platform well enough to run calls independently without senior support Manage active customer projects end-to-end: status updates, timeline management, and deliverable coordination through final report QC and co-deliver final customer data reports, ensuring outputs are scientifically accurate and on-scope Own CRM hygiene, pipeline forecasting, and opportunity tracking in Salesforce; contribute a short-term commercial forecast Represent Integral Molecular externally - at conferences, in webinars, presentations and bring market intelligence back to scientific and product leaders The ideal candidate will have Prior life sciences commercial experience: BD, sales, or application scientist role Proven ability to prospect, manage a pipeline, and close - not just support sales is desired Scientific storyteller: ability to translate complex science into value-driven business conversations. Comfortable presenting science to diverse buyers: discovery scientists, BD leaders, IP counsel PhD in biological sciences or related STEM field If you find this position appealing, please submit a resume and cover letter that outlines your interest in our company, your relevant experiences for this role, and salary expectations. Integral Molecular is an Equal Opportunity Employer.", "summaryDescription" : "Sales and Application Scientist – Protein Engineering (Non-Bench) at Integral Molecular. Skills: Protein Engineering, Sales, Application Science. Prospect and convert accounts. Vet technical feasibility", "postedDate" : "2026-06-11T21:07:10.763", "createdAt" : "2026-06-11T21:07:10.763", "lastUpdated" : "2026-06-14T22:15:12.063", "ingestTimestamp" : "2026-06-11T21:07:10.763", "mongoId" : "6a2a48eb74d8ee00a05e29a2", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 95000, "salaryAnnualMax" : 135000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Technical feasibility", "Risk assessment", "Protein Engineering", "Sales", "Application Science", "Commercial development", "Revenue targets", "Pipeline forecasting", "Opportunity tracking", "Market intelligence", "Timeline management", "Protein Engineering platform", "Biotech", "Pharma", "Therapeutics", "CRM" ], "skillCount" : 16, "jobCategory" : "other", "jobSubcategory" : "research", "dataQualityScore" : 0.7777778, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech" }, { "id" : "6a25061d74d8ee00a0090ffc", "title" : "Scientist, Cell-Based & Functional Assays", "company" : "Adaptyv", "industry" : "Biology", "salary" : { "min" : 105000.0, "max" : 145000.0, "currency" : "CHF", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Scientist, Cell-Based & Functional Assays in Biotech in Lausanne, Switzerland, adjusted for company size and industry." }, "location" : "Lausanne", "locations" : [ "Lausanne" ], "timestamp" : "2026-06-08T08:50:16.266", "fingerprint" : "83f43dcb60aa28c6dad6c4b964cfdf189487445d296b2fda5522d2a0d94218c6", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/adaptyv/9e938c23-156b-46dd-aae3-4d498b778bd3/application", "externalId" : "9e938c23-156b-46dd-aae3-4d498b778bd3", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Lausanne", "country" : "Switzerland", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "46.5218269,6.6327025" } ], "locationText" : "Lausanne, Switzerland", "employmentType" : "FULL_TIME", "technicalSkills" : "Cell-based assays, Functional assays, Potency assays, Reporter-gene assays, Flow cytometry, Antibody functional readouts, Agonism, Antagonism, ADCC, CDC, T-cell activation, Cytokine readouts, Data modeling", "professionalSkills" : [ "Assay development", "Assay qualification", "Assay validation", "Productization", "High-throughput", "Data interpretation", "Assay robustness", "Customer advising", "Internal advising" ], "hardSkillsList" : [ "Cell activation", "Signaling", "Dose-response analysis", "Potency analysis", "Normalization" ], "hardSkills" : [ { "name" : "Cell activation", "level" : "intermediate" }, { "name" : "Signaling", "level" : "intermediate" }, { "name" : "Dose-response analysis", "level" : "intermediate" }, { "name" : "Potency analysis", "level" : "intermediate" }, { "name" : "Normalization", "level" : "intermediate" } ], "majorSkills" : "Cell-based assays, Functional assays, Potency assays, Assay productization", "majorSkillsList" : [ "Cell-based assays", "Functional assays", "Potency assays", "Assay productization" ], "coreResponsibilities" : "Develop cell-based functional assays, Qualify cell-based functional assays, Run cell-based functional assays, Develop cell activation assays, Develop signaling assays, Develop reporter-gene assays, Develop potency assays, Develop antibody functional readouts, Turn bespoke assays into productized capabilities, Integrate assays into production workflows, Scale assays onto automated systems, Structure functional data, Model functional data, Make functional data interpretable, Make functional data comparable, Own assay robustness, Manage controls, Manage reference standards, Advise customers on assay design, Advise internal teams on assay design, Advise on functional data meaning", "teamCollaboration" : "Work with biology team; Work with lab automation; Work with software team", "domainKnowledge" : "Antibody function; Protein function; Mechanism of action; Cell activation; Receptor activation; Receptor blocking; Signaling pathways; Immune response modulation; Agonism; Antagonism; ADCC; CDC; T-cell activation; Cytokine production", "domainList" : [ "antibody-function", "protein-function", "mechanism-of-action", "cell-activation", "receptor-activation", "receptor-blocking", "signaling-pathways", "immune-response-modulation", "agonism", "antagonism", "adcc", "cdc", "t-cell-activation", "cytokine-production" ], "domainSpecificKnowledge" : [ "Antibody function", "Protein function", "Mechanism of action", "Cell activation", "Receptor activation", "Receptor blocking", "Signaling pathways", "Immune response modulation", "Agonism", "Antagonism", "ADCC", "CDC", "T-cell activation", "Cytokine production" ], "problemSolvingSkills" : "Troubleshooting", "outcomesObjectives" : "Define reproducible performance; Make data comparable across runs", "qualificationsBasic" : "Hands-on experience developing cell-based assays, Hands-on experience developing functional assays, Hands-on experience developing potency assays, Experience with reporter cell lines, Experience with primary cells, Experience with flow cytometry, Experience making cell assays reproducible, Applied industry experience in production setting, Applied industry experience in development setting, Applied industry experience in commercial setting, Understanding of antibody function, Understanding of protein function", "qualificationsPreferred" : "Data fluency is a plus, Scripting is a plus, Analyzing dose-response data is a plus, Analyzing potency data is a plus", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Adaptyv is building an automated lab thats let AI agents run biology experiments. We're entering the era of agentic science where AI models can now design novel proteins, propose hypotheses, and iterate on experimental results. But they can't run the experiments themselves - that's still a manual, months-long process. We're building the infrastructure that gives AI agents access to the physical world. We are one of the fastest growing biotech companies, trusted by leading biopharmas, frontier AI labs, and the techbio companies pushing the field forward. This is a rare chance to help advance some of the most important work happening in biotech today. Our automated lab is powered by a deep software + hardware stack: lab instruments worth millions of USD reverse-engineered into API-controllable hardware, dozens of devices orchestrated through complex workflows, full observability on everything that happens in the lab, processing pipelines for messy physical-world data, and AI systems that troubleshoot production results and accelerate assay development. We’re growing rapidly and are hiring for talented people to scale and support the massive demand for AI-driven wet lab experimentation. ABOUT THE ROLE You'll build out cell-based and functional assays at Adaptyv — the work that proves an antibody or protein actually does something: activates or blocks a receptor, triggers signaling, kills a cell, or modulates an immune response. Cell activation assays, reporter systems, potency assays, and antibody functional readouts are the heart of this role. This is the most interdisciplinary of our scientist roles. A new functional assay starts as bespoke science and has to become a reliable, automated product. You'll design and run the assays hands-on with the biology team, work with lab automation to make them robust and high-throughput, and work with the software team to capture, model, and interpret the data — turning messy cell-based readouts into clean, comparable results. You'll guide and lead, but the value is in setting up real, working assays, not in managing. WHAT YOU'LL DO - Develop, qualify, and run cell-based functional assays hands-on: cell activation and signaling, reporter-gene assays, potency assays, and antibody functional readouts (e.g. agonism/antagonism, ADCC/CDC-type functional effects, T-cell activation, cytokine readouts). - Turn bespoke functional assays into productized, orderable capabilities with defined, reproducible performance. - Work with the biology team to integrate assays into production workflows, and with lab automation to scale them onto automated systems. - Partner with the software team to structure and model functional data — dose-response, potency, normalization — and make it interpretable and comparable across runs. - Own assay robustness: controls, reference standards, troubleshooting, and the quality bar for what we report. - Advise customers and internal teams on assay design and what the functional data means. WHAT WE'RE LOOKING FOR - Deep, hands-on experience developing cell-based and functional/potency assays — reporter cell lines, primary cells, flow cytometry, and the realities of making cell assays reproducible. - Applied industry experience. You've built and run these assays in a production, development, or commercial setting where throughput and reliability mattered — not primarily in an academic research project. This is the core requirement. - Strong on antibody / protein function — you understand mechanism well enough to design the right assay for the question. - Builder who moves fast. You like standing up new assay capabilities and productizing them. - Genuinely interdisciplinary. You're energized by working across biology, automation, and software, and you treat data modeling and automation as part of the assay, not an afterthought. - Data fluency (scripting, analyzing dose-response and potency data) is a strong plus. DETAILS - Location: Lausanne, Switzerland (on-site) - Type: Full time - Start date: ASAP Application deadline We are reviewing applicants on a rolling basis.", "summaryDescription" : "Scientist, Cell-Based & Functional Assays at Adaptyv. Skills: Cell-based assays, Functional assays, Potency assays, Assay productization. Develop cell-based functional assays. Qualify cell-based functional assays", "postedDate" : "2026-06-07T09:28:26.679", "createdAt" : "2026-06-07T09:28:26.679", "lastUpdated" : "2026-06-08T08:50:16.266", "ingestTimestamp" : "2026-06-07T09:28:26.679", "mongoId" : "6a25061d74d8ee00a0090ffc", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Cell activation", "Signaling", "Dose-response analysis", "Potency analysis", "Normalization", "Cell-based assays", "Functional assays", "Potency assays", "Assay productization", "Assay development", "Assay qualification", "Assay validation", "Productization", "High-throughput", "Data interpretation", "Assay robustness", "Customer advising", "Internal advising", "Antibody function", "Protein function", "Mechanism of action", "Receptor activation", "Receptor blocking", "Signaling pathways", "Immune response modulation", "Agonism", "Antagonism", "ADCC", "CDC", "T-cell activation", "Cytokine production" ], "skillCount" : 31, "jobCategory" : "other", "jobSubcategory" : "biology", "dataQualityScore" : 0.8888889, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech" }, { "id" : "6a30704ff292fd229cff3317", "title" : "Behavioral Technician (Certification Included!)", "company" : "Cortica", "industry" : "Healthcare", "salary" : { "min" : 20.0, "max" : 27.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Carlsbad, California, United States", "locations" : [ "Carlsbad", "California", "United States" ], "timestamp" : "2026-06-16T11:10:30.044", "fingerprint" : "0b543b6370b649cc419ca98191b333b93f0ee35a32b8431d30513e81934e5642", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/allcareers/jobs/8593206002", "externalId" : "8593206002", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Carlsbad", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "33.1580933,-117.3505966" } ], "locationText" : "Carlsbad, California, United States", "employmentType" : "PART_TIME", "remoteFriendly" : false, "rawDescription" : "Title: Behavior Technician (Naturalistic, Play-Based ABA) Cortica is looking for dedicated, compassionate Behavior Technicians to join our growing team and help us design and deliver life-changing care for children with neurodevelopmental differences. At Cortica, we don’t just offer jobs; we offer careers with purpose, growth, and support. What We Offer: Pay Range: $20.57 to $27.60 per hour, based on experience and education. Thoughtfully Designed Schedules: We offer a predictable schedule with a single, direct rate of pay, including: Part-time roles with flexible 5-, 3- or 2-day-per-week options. Opportunities to pick up additional hours on Saturdays Fully Paid Training & Certification: Kickstart your career with Cortica with a comprehensive 2-week, in-person orientation that includes hands-on training, a Board-Certified Autism Technician (BCAT) exam review, and full coverage of your exam fees. We’re invested in your success from day one. Referral Bonus: Earn between $250-$500 for successful referrals. Cell Phone Stipend: Stay connected with support from us. Paid Drive Time and Mileage Reimbursement: We value your time on the road and include toll reimbursement in select areas. 401(k) with Company Matching: Secure your future with our generous plan. Ongoing Professional Development: Access continuous training through in-person and online opportunities. Supportive Environment: Collaborate with and receive expert coaching from Lead BTs, ABA Assistant Supervisors, and ABA Supervisors who champion your growth. Career Advancement: Opportunities to grow your career by advancing to a BCBA role, ascending the Behavior Technician Clinical Ladder, or serving in a corporate support role. Learn from Experts in Other Fields: Partner with BCBAs and experts in speech-language therapy, music therapy, occupational therapy, and physical therapy as well as counselors, pediatricians, neurologists, and nurse practitioners. Your Impact & Responsibilities: Provide 1:1 and group behavior-analytic services to children with autism and other neurodevelopmental differences. Implement positive behavior strategies developed with your BCBA. Use evidence-based practices to create meaningful progress for families. Document session data to track and support treatment goals. Collaborate closely with families and supervisors to build supportive environments. Follow Cortica's crisis protocols, including de-escalation and mandated reporting. Who We’re Looking For: Experience working with children (experience with autism is a plus!). High School or equivalent, bachelor’s or master’s degree. Willingness to obtain your BCAT credential within 90 days of your start date (We provide all training!). Ability to consistently travel between client sites within a 30–40-minute radius using reliable transportation. Tech-savvy with EMR systems and Microsoft Office tools. Our Inclusive Culture: Transdisciplinary Approach: Collaborate with experts in various fields to care for the whole child. Collaborative Process: Develop individualized care plans alongside families and clinicians. Strength-Based, Neurodiversity-Affirming Model: Focus on building on each child’s unique strengths rather than emphasizing deficits. Join Cortica’s team and make a meaningful impact by applying a strength-based, neurodiversity-affirming ABA therapy model. Help children recognize and build on their unique abilities, fostering positive relationships and skills that translate across home, school, and community settings. Be part of a progressive approach that combines neuroscience and developmental models to empower each child to thrive. Ready to make a difference? Apply today! Equal Opportunity Employer (EOE). For more details, visit the full job description here. Behavioral Health Center of Excellence (BHCOE) Accredited 2024 | America’s Greatest Midsize Workplaces 2025 Newsweek | Great Place to Work Certified 2025 | Glassdoor 4.3 Rating 2025 | Indeed 4.1 Rating 2025 Privacy Notice  https://corticacare.com/privacy-policyCortica is committed to protecting your personal information in compliance with applicable federal and state laws. Please review our Privacy Notice to understand how your data is collected, used, and protected.  Fair Chance Ordinance Compliance  Cortica is committed to fair hiring practices. Qualified candidates with criminal histories and/or driving violations will be considered and are not automatically disqualified from employment, consistent with applicable federal law, the California Fair Chance Act, and local ordinances.  Driving Requirement  This position requires the successful completion of a post-offer background check and a motor vehicle report review.  E-Verify Participation  This employer participates in E-Verify. Click here to view the E-Verify Poster and your Right to Work.  Este empleador participa en E-Verify. Este empleador participa en E-Verify. Haga clic aquí para ver el cartel de E-Verify y su derecho a trabajar.  #LI-JK1", "summaryDescription" : "Behavioral Technician (Certification Included!) at Cortica", "postedDate" : "2026-06-16T01:18:42.610", "createdAt" : "2026-06-16T01:18:42.610", "lastUpdated" : "2026-06-16T11:10:30.044", "ingestTimestamp" : "2026-06-16T01:18:42.610", "mongoId" : "6a30704ff292fd229cff3317", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 41600, "salaryAnnualMax" : 56160, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "healthcare", "jobSubcategory" : "support", "seniorityLevel" : "Entry", "dataQualityScore" : 0.7777778, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2c798f74d8ee00a0941da4", "title" : "Fanatics Collect (including Live) and Topps. com Global Legal Lead", "company" : "Fanatics Collectibles", "industry" : "E-Commerce", "salary" : { "min" : 195500.0, "max" : 285000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Los Angeles, California, United States", "locations" : [ "Los Angeles", "California", "United States", "New York", "New York", "United States" ], "timestamp" : "2026-06-15T08:08:56.730", "fingerprint" : "fcbd50bb99a6fa6d9330e683f477f3e26d72194c574648d5c0860ffa747617e4", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/fanaticscollectibles/jobs/4257712009", "externalId" : "4257712009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Los Angeles", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.0536909,-118.2427660" }, { "city" : "New York", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.7127281,-74.0060152" } ], "locationText" : "Los Angeles, California, United States; New York, New York, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 8, "experienceMaxYears" : 15, "experienceLevel" : "Lead", "professionalSkills" : [ "Legal analysis", "Risk management", "Compliance oversight", "Regulatory requirements" ], "hardSkillsList" : [ "Consumer protection law", "E-commerce law", "Digital payments", "Subscription models", "Loyalty programs", "Content regulation", "IP use", "User-generated content", "Influencer marketing", "Technology agreements", "Platform partnerships", "SaaS contracts", "Licensing contracts", "Vendor agreements", "Sweepstakes rules", "Promotional terms" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Consumer protection law", "level" : "intermediate" }, { "name" : "E-commerce law", "level" : "intermediate" }, { "name" : "Digital payments", "level" : "intermediate" }, { "name" : "Subscription models", "level" : "intermediate" }, { "name" : "Loyalty programs", "level" : "intermediate" }, { "name" : "Content regulation", "level" : "intermediate" }, { "name" : "IP use", "level" : "intermediate" }, { "name" : "User-generated content", "level" : "intermediate" }, { "name" : "Influencer marketing", "level" : "intermediate" }, { "name" : "Technology agreements", "level" : "intermediate" }, { "name" : "Platform partnerships", "level" : "intermediate" }, { "name" : "SaaS contracts", "level" : "intermediate" }, { "name" : "Licensing contracts", "level" : "intermediate" }, { "name" : "Vendor agreements", "level" : "intermediate" }, { "name" : "Sweepstakes rules", "level" : "intermediate" }, { "name" : "Promotional terms", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Digital platforms, Legal counsel, Compliance", "majorSkillsList" : [ "Digital platforms", "Legal counsel", "Compliance" ], "coreResponsibilities" : "Serve as primary legal advisor, Partner with product, engineering, design, marketing, privacy, compliance,, Provide pragmatic, solutions-oriented guidance, Advise on product features, Advise on user experiences, Advise on customer engagement strategies, Advise on go-to-market initiatives, Collaborate with international business and legal teams, Support global expansion, Support local market adaptations, Support cross-jurisdiction regulatory compliance, Advise on consumer protection issues, Advise on e-commerce law issues, Advise on digital payments issues, Advise on subscription models issues, Advise on loyalty/rewards programs issues, Advise on content regulation issues, Advise on IP use issues, Advise on user-generated content issues, Advise on influencer marketing issues, Draft agreements, Review agreements, Negotiate agreements, Develop global consumer-facing terms, Maintain global consumer-facing terms, Develop platform rules, Maintain platform rules, Develop privacy-related disclosures, Maintain privacy-related disclosures, Develop sweepstakes/contest rules, Maintain sweepstakes/contest rules, Develop promotional terms, Maintain promotional terms, Support privacy-by-design processes, Advise on global consent, Advise on data governance", "teamCollaboration" : "Global product teams; Global engineering teams; Global design teams; Global marketing teams; Global privacy teams; Global compliance teams; Global operations teams; International business teams; International legal teams", "domainKnowledge" : "Digital platforms; Technology; Global DTC; Sports collectibles industry; Sports memorabilia; Digital trading cards; Sports betting; Sportsbook; iGaming platform", "domainList" : [ "digital-platforms", "technology", "global-dtc", "sports-collectibles-industry", "sports-memorabilia", "digital-trading-cards", "sports-betting", "sportsbook", "igaming-platform" ], "domainSpecificKnowledge" : [ "Digital platforms", "Technology", "Global DTC", "Sports collectibles industry", "Sports memorabilia", "Digital trading cards", "Sports betting", "Sportsbook", "iGaming platform" ], "communicationSkills" : "Summarize advice; Expand analysis", "specialRequirements" : "Ability to travel frequently, Travel on short notice", "outcomesObjectives" : "Build world-class collector experiences; Ensure compliance across multiple jurisdictions; Ensure compliance across product categories", "qualificationsBasic" : "Prior comparable experience a must, Deep understanding of digital platforms, Deep understanding of technology", "qualificationsPreferred" : "Understanding of innovative legal topics", "workSiteFlexibility" : "Onsite", "rawDescription" : "About Us Fanatics is building a leading global digital sports platform. We ignite the passions of global sports fans and maximize the presence and reach for our hundreds of sports partners globally by offering products and services across Fanatics Commerce, Fanatics Collectibles, and Fanatics Betting collect physical and digital trading cards, sports memorabilia, and other digital assets; and bet as the company builds its Sportsbook and iGaming platform. Fanatics has an established database of over 100 million global sports fans; a global partner network with approximately 900 sports properties, including major national and international professional sports leagues, players associations, teams, colleges, college conferences and retail partners, 2,500 athletes and celebrities, and 200 exclusive athletes; and over 2,000 retail locations, including its Lids retail stores. Our more than 22,000 employees are committed to relentlessly enhancing the fan experience and delighting sports fans globally. About the Team Fanatics Collectibles is transforming the global collectibles industry by building the world’s most comprehensive, fan-focused ecosystem of physical and digital products. As part of Fanatics’ broader mission to create the ultimate digital sports platform where fans can buy, collect, and engage, we connect millions of collectors through platforms such as Topps.com, Fanatics Collect, Fanatics Live, and Topps Digital. The Legal team at Fanatics Collectibles is a key strategic partner to our product, engineering, operations, marketing, and business leadership teams. We enable innovation at speed while ensuring regulatory compliance, consumer trust, and long-term product integrity. Role Summary Fanatics Collectibles is seeking a seasoned lawyer to lead legal for Fanatics Collect, including Fanatics Live, and Topps.com as well future DTC platforms on a global basis. A deep understanding of digital platforms (Global DTC) and technology is essential for this role to support the global operations of such platforms. Prior comparable experience a must. The legal lead will serve as an embedded legal advisor throughout the full product lifecycle — from early ideation and design, to development, launch, and iteration across Topps.com, Fanatics Collect, Fanatics Live, Topps Digital, and future DTC platforms on a global basis. The legal lead will serve as primary overall counsel for these businesses covering all areas of legal, compliance and risk. This role requires a lawyer who not only understands technology, digital commerce, and platform risk, but who has a deep understanding of innovative legal topics and also shares our passion for relentlessly enhancing the collector experience. You will use your legal expertise to help build world-class collector experiences that are innovative, compliant, globally scalable, and grounded in fan trust. You will work cross-functionally with U. S. and international stakeholders to help shape product strategy, guide responsible innovation, and ensure compliance across multiple jurisdictions and product categories. A super exciting senior opportunity that involves working directly with our leadership team. The position is in-office and based in either New York or LA. Key Responsibilities Serve as the primary legal advisor for our global direct-to-consumer digital and mobile platforms (Topps.com, Fanatics Collect, Fanatics Live, Topps Digital and future platforms) across global markets. Partner closely with global product, engineering, design, marketing, privacy, compliance, and operations teams from concept through launch and lifecycle iteration. Provide pragmatic, solutions-oriented guidance on product features, user experiences, customer engagement strategies, and go-to-market initiatives worldwide. Collaborate effectively with international business and legal teams to support global expansion, local market adaptations, and cross-jurisdiction regulatory compliance. Advise on all issues on a general and global basis including issues related to consumer protection, e-commerce law, digital payments, subscription models, loyalty/rewards programs, content regulation, IP use, user-generated content, and influencer marketing. Draft, review, and negotiate all agreements to support our global platforms, including technology agreements, platform partnerships, SaaS and licensing contracts, and vendor agreements supporting product operations. Develop and maintain global consumer-facing terms and policies, including terms of use, platform rules, privacy-related disclosures (in coordination with our privacy team), sweepstakes/contest rules, and promotional terms. Support privacy-by-design processes and advise on global consent, data governance, cross-border data flows, and other privacy and data-use considerations. Monitor and interpret global regulatory developments affecting digital commerce, consumer engagement, digital content, advertising, and emerging technologies. Help develop scalable legal processes, workflows, and governance mechanisms to support efficient, compliant product development across global markets. Deliver internal training and guidance to business teams to promote strong compliance and product-risk awareness. Qualifications Juris Doctor (JD) from an accredited law school; admitted to practice in at least one U. S. state (in-house registration acceptable). 10+ years of legal experience, with at least 3 years advising on global direct-to-consumer technology, product, digital media, or e-commerce matters at a top law firm or in-house at a technology or consumer-facing company. Strong experience with consumer protection, e-commerce law, digital advertising/marketing, and data privacy (U. S. and ideally international). Demonstrated ability to provide practical, business-oriented legal advice in a fast-paced environment with competing priorities. Proven experience working with product, engineering, design, marketing, and operations teams and across global time zones. Excellent judgment, communication, and interpersonal skills; ability to translate complex legal concepts into clear, actionable guidance. Passion for innovation and for continuously enhancing the collector experience. Preferred: experience supporting marketplace or high-traffic consumer platforms; familiarity with IP/content licensing, sweepstakes/promotion rules, payment regulation, and global privacy frameworks such as GDPR and CPRA. Knowledge Skills and Abilities Be a doer whose ready, willing and able to roll up your sleeves, jump in and get things done. Be a self-starter with a strong work ethic, capable of taking ownership of projects/matters. Have a strong desire to assume a wide variety of responsibilities, be flexible and grow with the company. Able to accomplish multiple tasks at once while balancing competing objectives and deadlines. Produce high-quality carefully crafted work product in a timely manner. Have strong interpersonal skills and ability to forge strong relationships with key stakeholders throughout the organization. Work effectively both independently and as a team player in a team oriented environment, friendly and excited about “play nice” culture. Be confident, be a collaborator and initiative taker. Do not watch the clock, be flexible, invested, committed and immersed in the excitement about and commitment to the success of our businesses. Strong understanding of the Collectibles businesses and overall Fanatics operations. Be a creative thinker who can initiate and develop alternative approaches to complex issues. Have a “how” state of mind, not a yes/no advisor. Professional and have a perfect sense of integrity, reliable and does the right thing. Excellent organizational skills and attention to detail. Excellent legal and business acumen and problem-solving skills. Exceptional communication skills (verbal and written) with the ability to synthesize complex data for a range of audiences. Ability to advise all levels of seniority, summarize bottom line concise advice and in the same time able to expand to full spectrum of details and analysis as appropriate. Able to function in excellence in a high-paced, entrepreneurial and constantly evolving and fast-moving environment. Aim to be best in class – goal oriented and task focused learner who is innovative and influential. Driven to win, ambassador of the Fanatics brand who brings passion, energy and positivity into the workplace. Ability to travel frequently on short notice. Ensure your Fanatics job offer is legitimate and don’t fall victim to fraud. Fanatics never seeks payment from job applicants. Feel free to ask your recruiter for a phone call or other type of communication for interview, and ensure your communication is coming from a Fanatics email address (including @collectfanatics.com). For added security, where possible, apply through our company website at www.fanaticsinc.com/careers The salary range represents base pay only and does not include short-term or long-term incentive compensation. This salary range is specific to Los Angeles and may not be applicable to other locations. When determining base pay, as part of a final compensation package, we consider several factors such as location, experience, qualifications, and training. For information about our benefits, please visit https://benefitsatfanatics.com/ Los Angeles Salary Range $195,500—$285,000 USD The salary range represents base pay only and does not include short-term or long-term incentive compensation. This salary range is specific to New York City and may not be applicable to other locations. When determining base pay, as part of a final compensation package, we consider several factors such as location, experience, qualifications, and training. For information about our benefits, please visit https://benefitsatfanatics.com/ NYC Salary Range $212,500—$305,000 USD By submitting your application, you agree to our terms of service and acknowledge you have read our Candidate Privacy Policy.", "summaryDescription" : "Fanatics Collect (including Live) and Topps. com Global Legal Lead at Fanatics Collectibles. Skills: Digital platforms, Legal counsel, Compliance. Serve as primary legal advisor. Partner with product, engineering, design, marketing, privacy, compliance,", "postedDate" : "2026-06-14T03:09:49.984", "createdAt" : "2026-06-14T03:09:49.984", "lastUpdated" : "2026-06-15T08:08:56.730", "ingestTimestamp" : "2026-06-14T03:09:49.984", "mongoId" : "6a2c798f74d8ee00a0941da4", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 195500, "salaryAnnualMax" : 285000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Consumer protection law", "E-commerce law", "Digital payments", "Subscription models", "Loyalty programs", "Content regulation", "IP use", "User-generated content", "Influencer marketing", "Technology agreements", "Platform partnerships", "SaaS contracts", "Licensing contracts", "Vendor agreements", "Sweepstakes rules", "Promotional terms", "Leadership", "Digital platforms", "Legal counsel", "Compliance", "Legal analysis", "Risk management", "Compliance oversight", "Regulatory requirements", "Technology", "Global DTC", "Sports collectibles industry", "Sports memorabilia", "Digital trading cards", "Sports betting", "Sportsbook", "iGaming platform" ], "skillCount" : 32, "jobCategory" : "operations", "jobSubcategory" : "legal", "seniorityLevel" : "Executive", "dataQualityScore" : 1.0, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "E-Commerce", "llmIndustryConfidence" : 0.98 }, { "id" : "6a305b92f292fd229cf5ef8f", "title" : "Mitarbeiter ( BTA / MTLA / CTA / PTA ) – Produktion rekombinante Proteine – Downstream Processing (m|w|d)", "company" : "Miltenyi Biotec", "industry" : "Biotechnology", "salary" : { "min" : 48000.0, "max" : 65000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for Mid-level Biologics Production roles in Teterow, Germany, adjusted for industry and company size." }, "location" : "Teterow, Germany", "locations" : [ "Teterow", "Germany" ], "timestamp" : "2026-06-16T10:04:37.496", "fingerprint" : "ed461aabc3878276038bfda666a864a22e5df7ee541a200194b342e6a7b20316", "source" : "smartrecruiters", "language" : "de", "applyUrl" : "https://jobs.smartrecruiters.com/MiltenyiBiotec1/744000132170409-mitarbeiter-bta-mtla-cta-pta-produktion-rekombinante-proteine-downstream-processing-m-w-d-", "externalId" : "744000132170409", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Teterow", "country" : "Germany", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "53.7709505,12.5753569" } ], "locationText" : "Teterow, Germany", "employmentType" : "FULL_TIME", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "mid", "technicalSkills" : "Biotechnologie, Biochemie, MS-Office", "professionalSkills" : [ "Eigenverantwortliches Arbeiten", "Prozessoptimierung" ], "hardSkillsList" : [ "Proteinaufreinigung", "Ultrafiltration", "Diafiltration", "Endformulierung", "Produktionsanlagen Bedienung", "Prozessbegleitende Analytik", "Daten Auswertung" ], "hardSkills" : [ { "name" : "Proteinaufreinigung", "level" : "intermediate" }, { "name" : "Ultrafiltration", "level" : "intermediate" }, { "name" : "Diafiltration", "level" : "intermediate" }, { "name" : "Endformulierung", "level" : "intermediate" }, { "name" : "Produktionsanlagen Bedienung", "level" : "intermediate" }, { "name" : "Prozessbegleitende Analytik", "level" : "intermediate" }, { "name" : "Daten Auswertung", "level" : "intermediate" } ], "majorSkills" : "Proteinaufreinigung, Downstream Processing, GMP-konforme Aufreinigung", "majorSkillsList" : [ "Proteinaufreinigung", "Downstream Processing", "GMP-konforme Aufreinigung" ], "coreResponsibilities" : "Refolding-Prozesse durchführen, Chromatographische Aufreinigung durchführen, Ultra- und Diafiltration durchführen, Endformulierung der Proteine durchführen, Produktionsanlagen bedienen, Equipment und Chromatographiesäulen vorbereiten, Equipment und Chromatographiesäulen nachbereiten, Herstellprozesse im Reinraum durchführen, SOPs dokumentieren, Prozessbegleitende Analytik ausführen, Daten strukturiert auswerten, Herstellprozesse optimieren", "teamCollaboration" : "Engagiertes Team; Interkulturelles Umfeld", "domainKnowledge" : "Rekombinante Proteine; Therapeutische Anwendungen; Zelltherapien; Gentherapien; Krebsbehandlung; Autoimmunerkrankungen; GMP", "domainList" : [ "rekombinante-proteine", "therapeutische-anwendungen", "zelltherapien", "gentherapien", "krebsbehandlung", "autoimmunerkrankungen", "gmp" ], "domainSpecificKnowledge" : [ "Rekombinante Proteine", "Therapeutische Anwendungen", "Zelltherapien", "Gentherapien", "Krebsbehandlung", "Autoimmunerkrankungen", "GMP" ], "documentationSkills" : "SOPs dokumentieren", "continuousLearning" : "Individuelle Weiterbildung", "innovationCreativity" : "Entwicklung innovativer Therapien; Kreativität", "qualificationsBasic" : "Abgeschlossene Berufsausbildung (BTA, MTLA, CTA, PTA, Laborant), Studium (B.Sc.) in Biotechnologie, Biochemie, Gute MS-Office-Kenntnisse, Sichere Deutschkenntnisse, Sichere Englischkenntnisse", "qualificationsPreferred" : "Erfahrung in Aufreinigung bakterieller Proteine, Kenntnisse in proteinbiochemischen Methoden", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Seit 35 Jahren entwickeln wir einzigartige Lösungen für die biomedizinische Spitzenforschung sowie für neuartige Zell- und Gentherapien. Wir tragen dazu bei, medizinische Methoden zu revolutionieren, um Krebs und andere schwere Krankheiten zu besiegen. Uns kennzeichnet ein Arbeitsumfeld, das von Kreativität und eigenverantwortlichem Arbeiten geprägt ist. Bei Miltenyi Biotec arbeiten mehr als 5.000 Menschen aus über 75 Ländern zusammen und bilden die Basis für unseren nachhaltigen Erfolg. An unserem Standort in Teterow, in der Nähe von Rostock, werden Sie Teil der Abteilung „Microbial Products“. Sie arbeiten in einem engagierten Team, das sich mit der GMP-konformen Aufreinigung rekombinanter Proteine für therapeutische Anwendungen beschäftigt. Es erwartet Sie ein abwechslungsreiches Aufgabenfeld, in dem Sie aktiv an der Entwicklung und Umsetzung innovativer Therapien zur Behandlung von Krebs und Autoimmunerkrankungen mitwirken. * Sie führen Refolding-Prozesse, die chromatographische Aufreinigung sowie die Ultra- und Diafiltration bis hin zur Endformulierung der Proteine eigenständig durch. * Auch die Bedienung der Produktionsanlagen sowie die Vor- und Nachbereitung des Equipments und der Chromatographiesäulen liegen in Ihrem Verantwortungsbereich. * Die Herstellprozesse werden im Reinraum durchgeführt und gemäß den vorgegebenen SOPs dokumentiert. * Die prozessbegleitende Analytik wird von Ihnen ausgeführt und die gewonnenen Daten werden strukturiert ausgewertet. * In die kontinuierliche Optimierung der Herstellprozesse bringen Sie Ihre Erfahrung aktiv ein. ## Qualifications * Vorausgesetzt wird eine abgeschlossene Berufsausbildung bspw. im naturwissenschaftlichen, technischen Bereich (z. B. BTA, MTLA, CTA, PTA oder Laborant) oder ein Studium (B.Sc.) in Biotechnologie, Biochemie. Quereinsteiger, die Neues erlernen wollen und Freude an technischem Arbeiten mitbringen, sind gerne willkommen. * Idealerweise konnten Sie bereits Erfahrung in der Aufreinigung bakterieller Proteine sammeln und bringen Kenntnisse in proteinbiochemischen Methoden mit. * Eine sorgfältige, strukturierte und präzise Arbeitsweise zeichnet Sie aus. * Als Teamplayer sind Sie zuverlässig, hilfsbereit sowie aufgeschlossen in Ihrer Kommunikation. * Gute MS-Office-Kenntnisse sowie sichere Deutsch- und Englischkenntnisse in Wort und Schrift runden Ihr Profil ab. ## Additional Information Was wir bieten * Arbeiten mit freier und selbstbestimmter Zeiteinteilung * Ein interkulturelles Umfeld, geprägt von Vielfalt, flachen Hierarchien, Duz-Kultur * Freiräume, um sich kreativ einzubringen und aktiv mitzugestalten * Individuelle Weiterbildung in unserer Miltenyi University als Kern der Miltenyi DNA * 30-Tage-Urlaub, vergünstigtes Deutschlandticket, (E)-Bike-Leasing, vermögenswirksame Leistungen, betriebliche Altersvorsorge, Berufsunfähigkeitsversicherung, Kantine u.v.m. Vielfalt ist die Grundlage unserer Kreativität bei Miltenyi Biotec. Bringen Sie sich ein, so wie Sie sind – unabhängig von Geschlecht, sexueller Identität, Alter, Herkunft, Religion oder Behinderung. Wir freuen uns auf Ihre Bewerbung Wenn Sie in einem offenen, kreativen und hilfsbereiten Team arbeiten möchten, bieten wir Ihnen hier das richtige Umfeld. Wir freuen uns auf Ihre Bewerbung – mit Ihrer Gehaltsvorstellung und Verfügbarkeit.", "summaryDescription" : "Mitarbeiter ( BTA / MTLA / CTA / PTA ) – Produktion rekombinante Proteine – Downstream Processing (m|w|d) at Miltenyi Biotec. Skills: Proteinaufreinigung, Downstream Processing, GMP-konforme Aufreinigung. Refolding-Prozesse durchführen. Chromatographische Aufreinigung durchführen", "postedDate" : "2026-06-15T10:56:36.000", "createdAt" : "2026-06-16T00:04:33.106", "lastUpdated" : "2026-06-16T10:04:37.496", "ingestTimestamp" : "2026-06-16T00:04:33.106", "mongoId" : "6a305b92f292fd229cf5ef8f", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ "Proteinaufreinigung", "Ultrafiltration", "Diafiltration", "Endformulierung", "Produktionsanlagen Bedienung", "Prozessbegleitende Analytik", "Daten Auswertung", "Downstream Processing", "GMP-konforme Aufreinigung", "Eigenverantwortliches Arbeiten", "Prozessoptimierung", "Rekombinante Proteine", "Therapeutische Anwendungen", "Zelltherapien", "Gentherapien", "Krebsbehandlung", "Autoimmunerkrankungen", "GMP" ], "skillCount" : 18, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a304fbdf292fd229cee9ab2", "title" : "Mitarbeiter ( BTA / MTLA / CTA / PTA ) – Produktion rekombinante Proteine – Downstream Processing (m|w|d)", "company" : "Miltenyi Biotec", "industry" : "Biotechnology", "salary" : { "min" : 48000.0, "max" : 65000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Mid-level Mitarbeiter (BTA/MTLA/CTA/PTA) in Biotech production (Downstream Processing) in Teterow, Germany, adjusted for industry and location." }, "location" : "Teterow, Germany", "locations" : [ "Teterow", "Germany" ], "timestamp" : "2026-06-16T06:40:12.885", "fingerprint" : "d3918d5a2273e9d28a90f4295cdb9f0597663a6b487cbd1a9c80de83ca938ce3", "source" : "smartrecruiters", "language" : "de", "applyUrl" : "https://jobs.smartrecruiters.com/MiltenyiBiotec1/744000132170409-mitarbeiter-bta-mtla-cta-pta-produktion-rekombinante-proteine-downstream-processing-m-w-d-", "externalId" : "744000132170409", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Teterow", "country" : "Germany", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "53.7709505,12.5753569" } ], "locationText" : "Teterow, Germany", "employmentType" : "FULL_TIME", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "mid", "technicalSkills" : "Biotechnologie, Biochemie, MS-Office", "professionalSkills" : [ "Eigenverantwortliches Arbeiten", "Prozessoptimierung" ], "hardSkillsList" : [ "Refolding-Prozesse", "Chromatographische Aufreinigung", "Ultrafiltration", "Diafiltration", "Endformulierung", "Produktionsanlagen Bedienung", "Equipment Vorbereitung", "Equipment Nachbereitung", "Chromatographiesäulen Vorbereitung", "Chromatographiesäulen Nachbereitung", "Reinraum", "SOPs Dokumentation", "Prozessbegleitende Analytik", "Daten Auswertung" ], "hardSkills" : [ { "name" : "Refolding-Prozesse", "level" : "intermediate" }, { "name" : "Chromatographische Aufreinigung", "level" : "intermediate" }, { "name" : "Ultrafiltration", "level" : "intermediate" }, { "name" : "Diafiltration", "level" : "intermediate" }, { "name" : "Endformulierung", "level" : "intermediate" }, { "name" : "Produktionsanlagen Bedienung", "level" : "intermediate" }, { "name" : "Equipment Vorbereitung", "level" : "intermediate" }, { "name" : "Equipment Nachbereitung", "level" : "intermediate" }, { "name" : "Chromatographiesäulen Vorbereitung", "level" : "intermediate" }, { "name" : "Chromatographiesäulen Nachbereitung", "level" : "intermediate" }, { "name" : "Reinraum", "level" : "intermediate" }, { "name" : "SOPs Dokumentation", "level" : "intermediate" }, { "name" : "Prozessbegleitende Analytik", "level" : "intermediate" }, { "name" : "Daten Auswertung", "level" : "intermediate" } ], "majorSkills" : "Proteinaufreinigung, GMP-konforme Produktion, Biopharmazeutische Produktion", "majorSkillsList" : [ "Proteinaufreinigung", "GMP-konforme Produktion", "Biopharmazeutische Produktion" ], "coreResponsibilities" : "Durchführung von Refolding-Prozessen, Durchführung chromatographischer Aufreinigung, Durchführung Ultra- und Diafiltration, Durchführung Endformulierung der Proteine, Bedienung der Produktionsanlagen, Vorbereitung des Equipments, Nachbereitung des Equipments, Vorbereitung der Chromatographiesäulen, Nachbereitung der Chromatographiesäulen, Durchführung von Herstellprozessen im Reinraum, Dokumentation gemäß SOPs, Ausführung prozessbegleitender Analytik, Strukturierte Auswertung von Daten, Einbringung von Erfahrung in Prozessoptimierung", "teamCollaboration" : "Engagiertes Team; Interkulturelles Umfeld", "domainKnowledge" : "Rekombinante Proteine; Downstream Processing; Zell- und Gentherapien; Krebsbehandlung; Autoimmunerkrankungen; Biopharmazeutische Therapien; GMP-konforme Aufreinigung", "domainList" : [ "rekombinante-proteine", "downstream-processing", "zell-und-gentherapien", "krebsbehandlung", "autoimmunerkrankungen", "biopharmazeutische-therapien", "gmp-konforme-aufreinigung" ], "domainSpecificKnowledge" : [ "Rekombinante Proteine", "Downstream Processing", "Zell- und Gentherapien", "Krebsbehandlung", "Autoimmunerkrankungen", "Biopharmazeutische Therapien", "GMP-konforme Aufreinigung" ], "documentationSkills" : "SOPs Dokumentation", "continuousLearning" : "Individuelle Weiterbildung", "innovationCreativity" : "Entwicklung innovativer Therapien; Freiräume zur Mitgestaltung", "qualificationsBasic" : "Abgeschlossene Berufsausbildung (BTA, MTLA, CTA, PTA, Laborant), Studium (B.Sc.) in Biotechnologie, Biochemie, Gute MS-Office-Kenntnisse, Sichere Deutschkenntnisse, Sichere Englischkenntnisse", "qualificationsPreferred" : "Erfahrung in Aufreinigung bakterieller Proteine, Kenntnisse in proteinbiochemischen Methoden", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Seit 35 Jahren entwickeln wir einzigartige Lösungen für die biomedizinische Spitzenforschung sowie für neuartige Zell- und Gentherapien. Wir tragen dazu bei, medizinische Methoden zu revolutionieren, um Krebs und andere schwere Krankheiten zu besiegen. Uns kennzeichnet ein Arbeitsumfeld, das von Kreativität und eigenverantwortlichem Arbeiten geprägt ist. Bei Miltenyi Biotec arbeiten mehr als 5.000 Menschen aus über 75 Ländern zusammen und bilden die Basis für unseren nachhaltigen Erfolg. An unserem Standort in Teterow, in der Nähe von Rostock, werden Sie Teil der Abteilung „Microbial Products“. Sie arbeiten in einem engagierten Team, das sich mit der GMP-konformen Aufreinigung rekombinanter Proteine für therapeutische Anwendungen beschäftigt. Es erwartet Sie ein abwechslungsreiches Aufgabenfeld, in dem Sie aktiv an der Entwicklung und Umsetzung innovativer Therapien zur Behandlung von Krebs und Autoimmunerkrankungen mitwirken. * Sie führen Refolding-Prozesse, die chromatographische Aufreinigung sowie die Ultra- und Diafiltration bis hin zur Endformulierung der Proteine eigenständig durch. * Auch die Bedienung der Produktionsanlagen sowie die Vor- und Nachbereitung des Equipments und der Chromatographiesäulen liegen in Ihrem Verantwortungsbereich. * Die Herstellprozesse werden im Reinraum durchgeführt und gemäß den vorgegebenen SOPs dokumentiert. * Die prozessbegleitende Analytik wird von Ihnen ausgeführt und die gewonnenen Daten werden strukturiert ausgewertet. * In die kontinuierliche Optimierung der Herstellprozesse bringen Sie Ihre Erfahrung aktiv ein. ## Qualifications * Vorausgesetzt wird eine abgeschlossene Berufsausbildung bspw. im naturwissenschaftlichen, technischen Bereich (z. B. BTA, MTLA, CTA, PTA oder Laborant) oder ein Studium (B.Sc.) in Biotechnologie, Biochemie. Quereinsteiger, die Neues erlernen wollen und Freude an technischem Arbeiten mitbringen, sind gerne willkommen. * Idealerweise konnten Sie bereits Erfahrung in der Aufreinigung bakterieller Proteine sammeln und bringen Kenntnisse in proteinbiochemischen Methoden mit. * Eine sorgfältige, strukturierte und präzise Arbeitsweise zeichnet Sie aus. * Als Teamplayer sind Sie zuverlässig, hilfsbereit sowie aufgeschlossen in Ihrer Kommunikation. * Gute MS-Office-Kenntnisse sowie sichere Deutsch- und Englischkenntnisse in Wort und Schrift runden Ihr Profil ab. ## Additional Information Was wir bieten * Arbeiten mit freier und selbstbestimmter Zeiteinteilung * Ein interkulturelles Umfeld, geprägt von Vielfalt, flachen Hierarchien, Duz-Kultur * Freiräume, um sich kreativ einzubringen und aktiv mitzugestalten * Individuelle Weiterbildung in unserer Miltenyi University als Kern der Miltenyi DNA * 30-Tage-Urlaub, vergünstigtes Deutschlandticket, (E)-Bike-Leasing, vermögenswirksame Leistungen, betriebliche Altersvorsorge, Berufsunfähigkeitsversicherung, Kantine u.v.m. Vielfalt ist die Grundlage unserer Kreativität bei Miltenyi Biotec. Bringen Sie sich ein, so wie Sie sind – unabhängig von Geschlecht, sexueller Identität, Alter, Herkunft, Religion oder Behinderung. Wir freuen uns auf Ihre Bewerbung Wenn Sie in einem offenen, kreativen und hilfsbereiten Team arbeiten möchten, bieten wir Ihnen hier das richtige Umfeld. Wir freuen uns auf Ihre Bewerbung – mit Ihrer Gehaltsvorstellung und Verfügbarkeit.", "summaryDescription" : "Mitarbeiter ( BTA / MTLA / CTA / PTA ) – Produktion rekombinante Proteine – Downstream Processing (m|w|d) at Miltenyi Biotec. Skills: Proteinaufreinigung, GMP-konforme Produktion, Biopharmazeutische Produktion. Durchführung von Refolding-Prozessen. Durchführung chromatographischer Aufreinigung", "postedDate" : "2026-06-15T10:56:36.000", "createdAt" : "2026-06-15T21:36:22.290", "lastUpdated" : "2026-06-16T06:40:12.885", "ingestTimestamp" : "2026-06-15T21:36:22.290", "mongoId" : "6a304fbdf292fd229cee9ab2", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ "Refolding-Prozesse", "Chromatographische Aufreinigung", "Ultrafiltration", "Diafiltration", "Endformulierung", "Produktionsanlagen Bedienung", "Equipment Vorbereitung", "Equipment Nachbereitung", "Chromatographiesäulen Vorbereitung", "Chromatographiesäulen Nachbereitung", "Reinraum", "SOPs Dokumentation", "Prozessbegleitende Analytik", "Daten Auswertung", "Proteinaufreinigung", "GMP-konforme Produktion", "Biopharmazeutische Produktion", "Eigenverantwortliches Arbeiten", "Prozessoptimierung", "Rekombinante Proteine", "Downstream Processing", "Zell- und Gentherapien", "Krebsbehandlung", "Autoimmunerkrankungen", "Biopharmazeutische Therapien", "GMP-konforme Aufreinigung" ], "skillCount" : 26, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 1.0, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a3065e2f292fd229cfac31b", "title" : "Trade Management and Support Officer", "company" : "Circle K Energy Trading SA", "industry" : "Retail", "salary" : { "min" : 1800.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : false }, "location" : "Latvia", "locations" : [ "Latvia" ], "timestamp" : "2026-06-16T12:43:03.808", "fingerprint" : "92aa2a41b97c281e97e951014d4d04741538bcf7d7c0d5bba903334ea10b4996", "source" : "workday", "language" : "en", "applyUrl" : "https://circlek.wd3.myworkdayjobs.com/CircleKStoreJobs/job/Support-Office-Riga-BC--BU/Trade-Management-and-Support-Officer_R597584-1", "externalId" : "R597584", "industryFunction" : { }, "locationPoint" : "56.8796,24.6032", "structuredLocations" : [ { "city" : "Riga", "country" : "Latvia", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "56.9493977,24.1051846" } ], "locationText" : "Riga, Latvia", "minimumEducation" : "Master's", "technicalSkills" : "Power BI", "professionalSkills" : [ "Trade setup", "Pricing formula modelling", "Data validation", "Process improvements" ], "hardSkillsList" : [ "Excel proficiency", "System proficiency", "Data handling" ], "hardSkills" : [ { "name" : "Excel proficiency", "level" : "intermediate" }, { "name" : "System proficiency", "level" : "intermediate" }, { "name" : "Data handling", "level" : "intermediate" } ], "majorSkills" : "Trade management, ETRM system, Data accuracy", "majorSkillsList" : [ "Trade management", "ETRM system", "Data accuracy" ], "coreResponsibilities" : "Perform trade setup, Validate trade setup, Model pricing formulas, Quotations, Ensure compliance, Validate trade documentation, Validate system setups, Resolve discrepancies, Manage trade capture, Validate trade capture, Oversee process, Ensure end-to-end compliance, Contribute to process improvements, Contribute to simplification initiatives", "teamCollaboration" : "Coordinate with stakeholders; Collaborate across teams", "domainKnowledge" : "Energy market; Trading activities; Master Data; Business; Finance; Economics", "domainList" : [ "energy-market", "trading-activities", "master-data", "business", "finance", "economics" ], "domainSpecificKnowledge" : [ "Energy market", "Trading activities", "Master Data", "Business", "Finance", "Economics" ], "toolProficiency" : [ "Excel", "Power BI", "ETRM" ], "communicationSkills" : "Verbal English; Written English", "problemSolvingSkills" : "Analytical skills; Deep-dive into pricing", "qualificationsBasic" : "Master's degree, Analytical skills, Manage multiple tasks, Adapt to dynamic environment, Proficiency in Excel, Proficiency in Power BI, System skills, Handle large datasets, Interpersonal skills, Communication skills, Excellent English skills", "qualificationsPreferred" : "ETRM experience, Master Data experience, ERP experience, Accounting systems experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Job Description** **Circle K Energy Trading SA** is part of the Global Fuels organization and is responsible for fuel supply and trading activities across Europe. Our mission is to ensure efficient, compliant, and optimized trading operations in a rapidly evolving energy market. Trade Management and Support function plays an important role in ensuring data compliance and accuracy within the ETRM system, while coordinating closely with market traders, supply operations, finance, and other stakeholders to support smooth and efficient trading processes. This role is essential for maintaining operational excellence and supporting the CKETS Trading Team in Geneva from the Circle K Business Centre in Riga. **Circle K Business Centre in Riga, Latvia** is looking for: **Trade Management and Support Officer** **Type of Employment:** Permanent **Location** : Riga, Latvia **Visa requirements:** A valid work permit from the EU/EEA (relocation assistance is not provided) **Main Responsibilities:** * Perform detailed trade setup and validation within the ETRM system. Ensure accurate pricing formula modelling, fuel quotations, and alignment with commercial terms. * Ensure compliance with internal controls and requirements, validating trade documentation and system setups. * Coordinate with internal stakeholders to resolve discrepancies between commercial contracts and ETRM deal setups. * Manage and validate trade capture promptly after commercial transactions have been agreed upon. * Oversee the process through final execution, settlement, and payment, while ensuring end-to-end compliance and accuracy. * Leverage ETRM expertise and a strong understanding of trading activities. to contribute to process improvements and simplification initiatives within the function. **Main requirements:** * Degree in Master Data, Business, Finance, Economics, or a related field. * Strong analytical skills with the ability to deep-dive into pricing formulas. * Ability to manage multiple tasks, support diverse stakeholders simultaneously, and adapt effectively to a dynamic trading environment. * Proficiency in Excel and Power BI, with strong system skills and experience handling large datasets. * Strong interpersonal and communication skills, with the ability to communicate effectively and collaborate across teams. * Excellent written and verbal English skills for communication with colleagues across Europe. * Experience with ETRM, Master Data, ERP, or accounting systems is considered an advantage. **What you can expect at Circle K:** * For 6 years in a row, Circle K Business Centre has been awarded 1st place in the ‘CV-Online TOP Employer - International Business Services category.’ * Monthly salary:**starting from 1800 EUR** gross. * Covered tariff plan for your mobile phone. * Health insurance. * Employee discounts in our stores. * And more! **Interested?** We encourage you to apply by **June 30, 2026!** **We are looking forward to your application!** _**Circle K Business Centre SIA**_ _PVN Nr: LV40103511774_ _Duntes iela 6, Rīga, Latvija LV-1013_", "summaryDescription" : "Trade Management and Support Officer at Circle K Energy Trading SA. Skills: Trade management, ETRM system, Data accuracy. Perform trade setup. Validate trade setup", "postedDate" : "2026-06-16T03:48:54.991", "createdAt" : "2026-06-16T03:48:54.955", "lastUpdated" : "2026-06-16T12:43:03.808", "ingestTimestamp" : "2026-06-16T03:48:54.955", "mongoId" : "6a3065e2f292fd229cfac31b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://circlek.wd3.myworkdayjobs.com/CircleKStoreJobs/job/Support-Office-Riga-BC--BU/Trade-Management-and-Support-Officer_R597584-1", "salaryBand" : "<30k", "hasSalary" : false, "allSkills" : [ "Excel proficiency", "System proficiency", "Data handling", "Trade management", "ETRM system", "Data accuracy", "Trade setup", "Pricing formula modelling", "Data validation", "Process improvements", "Energy market", "Trading activities", "Master Data", "Business", "Finance", "Economics", "Excel", "Power BI", "ETRM" ], "skillCount" : 19, "jobCategory" : "finance", "jobSubcategory" : "accounting", "seniorityLevel" : "mid", "dataQualityScore" : 0.7777778, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Energy", "llmIndustryConfidence" : 0.95 }, { "id" : "6a3058bdf292fd229cf43fb0", "title" : "EHR and Billing Support Specialist", "company" : "Sourcefit", "industry" : "Healthcare", "salary" : { "min" : 600000.0, "max" : 900000.0, "currency" : "PHP", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level EHR and Billing Support Specialist in Quezon City, Philippines, adjusted for the healthcare industry." }, "location" : "Bridgetowne Quezon City, Philippines, PH", "locations" : [ "Bridgetowne Quezon City", "Philippines", "PH" ], "timestamp" : "2026-06-16T07:26:11.420", "fingerprint" : "e303d2761da72ab34d80b83cd91bece35748c2aa3f14f90a1c17c668af7fc24f", "source" : "breezyhr", "language" : "en", "applyUrl" : "https://sourcefit.breezy.hr/p/072ac1a28fec-ehr-and-billing-support-specialist", "externalId" : "072ac1a28fec", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Quezon City", "state" : "Metro Manila", "country" : "Philippines", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "14.6510546,121.0486254" } ], "locationText" : "Quezon City, Metro Manila, Philippines", "employmentType" : "FULL_TIME", "majorSkills" : "EHR, Billing support", "majorSkillsList" : [ "EHR", "Billing support" ], "coreResponsibilities" : "Provide EHR support, Provide billing support, Troubleshoot EHR issues, Troubleshoot billing issues, Assist users with EHR, Assist users with billing", "domainKnowledge" : "EHR systems; Medical billing", "domainList" : [ "ehr-systems", "medical-billing" ], "domainSpecificKnowledge" : [ "EHR systems", "Medical billing" ], "problemSolvingSkills" : "Troubleshooting", "qualificationsBasic" : "EHR experience, Billing support experience", "remoteFriendly" : true, "workSiteFlexibility" : "Onsite", "summaryDescription" : "EHR and Billing Support Specialist at Sourcefit. Skills: EHR, Billing support. Provide EHR support. Provide billing support", "createdAt" : "2026-06-15T22:11:34.728", "lastUpdated" : "2026-06-16T07:26:11.420", "ingestTimestamp" : "2026-06-15T22:11:34.728", "mongoId" : "6a3058bdf292fd229cf43fb0", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "EHR", "Billing support", "EHR systems", "Medical billing" ], "skillCount" : 4, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.9 }, { "id" : "6a3058cdf292fd229cf44257", "title" : "DOT Compliance and Administrative Support Specialist", "company" : "Terrestris Global Solutions", "industry" : "Logistics", "salary" : { "min" : 42500.0, "max" : 57500.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an Entry-level DOT Compliance and Administrative Support Specialist in Springfield, United States, adjusted for the logistics industry and company size." }, "location" : "Springfield, VA", "locations" : [ "Springfield", "VA" ], "timestamp" : "2026-06-16T06:39:02.929", "fingerprint" : "b8239b6ecf8f70222f023e1f1862ec0dea93b32be5a0c69dab7fdd1c53e5352e", "source" : "breezyhr", "language" : "en", "applyUrl" : "https://terrestris-global-solutions.breezy.hr/p/820c373f6c0301-dot-compliance-and-administrative-support-specialist", "externalId" : "820c373f6c0301", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Springfield", "state" : "Virginia", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.7749935,-77.1803819" } ], "locationText" : "Springfield, Virginia, United States", "employmentType" : "FULL_TIME", "coreResponsibilities" : "Support vehicle fleet operations, Support operations", "domainKnowledge" : "DOT compliance", "domainList" : [ "dot-compliance" ], "domainSpecificKnowledge" : [ "DOT compliance" ], "workSiteFlexibility" : "Onsite", "rawDescription" : "Are you looking for a Challenge? 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Sc. or Ph. D., Biochemistry, Biotechnology, or related discipline, hands-on experience with protein design, multiple expression systems (HEK293, CHO, E. coli), protein purification (Äkta), protein characterization (SEC, RP-HPLC)", "qualificationsPreferred" : "Initial experience in biopharmaceutical development, USP/DSP experience is a plus", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Do you enjoy solving complex scientific problems at the bench and seeing your work directly contribute to therapeutic development to improve patients' lives? Are you motivated by high-quality science, ownership of your experiments, and the opportunity to improve how things are done? Do you thrive in a small, collaborative team where your ideas have real impact? Then this could be your next career step. As an (Associate) Scientist in Protein Sciences, you will play a key role in the production and characterization of therapeutic protein candidates from research through development. You will combine hands-on laboratory work with scientific thinking to drive continuous process improvement and technology development by: * Developing and optimizing protein production workflows (cloning, expression, purification) * Performing protein characterization (purity, yield, stability, activity) * Contributing to scientific ideas and experimental strategies to advance projects * Analyzing, interpreting, and presenting data to cross-functional teams * Collaborating with CROs, CDMOs, and external partners * Preparing SOPs, reports, and scientific documentation * Staying up to date with scientific literature and emerging technologies **Requirements** * M.Sc. or Ph.D. in Biochemistry, Biotechnology, or a related discipline * Strong hands-on experience with protein design, multiple expression systems (HEK293, CHO, E. coli), and protein purification (Äkta) and characterization (e.g. SEC, RP-HPLC). * Initial experience in biopharmaceutical development (e.g. USP/DSP) is a plus * You combine scientific curiosity with strong critical thinking skills * You have a pragmatic, hands-on, and independent approach to experimental work * You work in a structured and detail-oriented manner * You communicate clearly and collaborate effectively in cross-functional teams **Benefits** * Remuneration package: An attractive salary, a sponsored pension scheme (bAV), and exciting short- and long-term incentives * Onboarding: Structured, well-proven onboarding program to give you a clear picture of your responsibilities and the company you will be working for * Training: Internal & external trainings and conferences embedded in a well-resourced training budget * Transport connections: Good connection to tram station, parking lots for cars and bikes * Mobility: You decide whether you want to use public transport with a discount or lease a JobBike * Food & more: Free lunch every day, soft drinks, fresh fruit, a wide variety of snacks * Equipment: State of the art, an iPhone and a laptop", "summaryDescription" : "(Associate) Scientist Protein Sciences (f/m/d) at Ascendis Pharma. Skills: Protein Sciences, Therapeutic development, Laboratory work. Develop protein production workflows. Optimize protein production workflows", "postedDate" : "2026-06-10T00:00:00.000", "createdAt" : "2026-06-12T22:36:01.912", "lastUpdated" : "2026-06-15T00:31:48.897", "ingestTimestamp" : "2026-06-12T22:36:01.912", "mongoId" : "6a2c5daa74d8ee00a08dd9b3", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://apply.workable.com/j/F2B49C7F6F", "salaryBand" : "50k-75k", "hasSalary" : false, "allSkills" : [ "Protein production", "Protein characterization", "Process improvement", "Technology development", "Critical thinking", "Protein Sciences", "Therapeutic development", "Laboratory work", "Scientific curiosity", "Experimental work", "Scientific documentation", "Biopharmaceutical development", "Äkta" ], "skillCount" : 13, "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "daysOld" : 5, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a0aaa1b1663d49372db0362", "title" : "Staff Scientist - Cancer Research and RNA-Based Therapeutics", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 175000.0, "max" : 250000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Lead Staff Scientist in Monrovia, California, adjusted for the biotech industry and senior experience level." }, "location" : "United States-California-Monrovia", "locations" : [ "United States-California-Monrovia", "Systems Biology", "Onsite, Days, Days" ], "timestamp" : "2026-06-15T22:26:24.994", "fingerprint" : "09c42ce369e05228d50832353c7396bf6c72f45d12714ba59004228ab8811385", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=238585", "externalId" : "238585", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Monrovia", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.1483499,-118.0014517" } ], "locationText" : "Monrovia, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "PhD", "experienceMinYears" : 3, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "remoteFriendly" : false, "rawDescription" : "Join the forefront of groundbreaking research at City of Hope where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research. The laboratory of Dr. Jianjun Chen is in search of a talented Staff Scientist. Our group is interested in discovering novel genetic and epigenetic regulations and deciphering their underlying molecular mechanisms in normal developmental processes and tumorigenesis. Our research spans multiple areas, including RNA Biology, Cancer Biology, Chromatin and Epigenetic Regulation, Cancer Metabolism, Immunology, Drug Discovery and Development, and Structural Biology, with a particular emphasis on RNA epigenetics/epitranscriptomics (RNA modifications) and RNA-based therapeutics . A major focus of our translational efforts is the development of mRNA-based therapeutics, particularly in vivo CAR-T/NK/Macrophage technologies and cancer mRNA vaccines, as well as epitranscriptomics-based biomarkers for cancer diagnosis, prognosis, and therapeutic response prediction. Our research involves experiments with RNA Biology, RNA modifications/editing, mRNA-based therapeutics, lipid nanoparticle (LNP) and alternative delivery systems, targeted delivery, cancer immunology, auto immune disease, primary human cancer cells, cancer and stem cell transplantation models, mouse genetics, molecular biology, biochemistry and cell biology, chemical biology, immunology, functional genomics, CARIPSR screening, signal transduction, single-cell sequencing, spatial sequencing, metabolism, drug development, structural biology, and large-scale data analysis and computational biology. For more information about Dr. Chen’s lab, please visit here. As a successful candidate, you will: Engage in a variety of advanced techniques, including but not limited to mRNA-based technologies, LNP development, targeted delivery, Flow cytometry, mass spectrometry/quantitative phospho-profiling, CyTOF, mouse genetics models, xenograft assays, retroviral gene delivery, chemical biology, drug development, whole exome sequencing and RNA-seq-analysis of clonal evolution of cancer, dot blots, RNA modification-seq, ChIP-seq, RIP-seq, PAR-CLIP-seq, single-cell sequencing, spatial sequencing, metabolism profiling, and pre-clinical drug testing in xenotransplantation models, etc. Your qualifications should include: A Ph.D. and/or M.D. degree(s), and a solid background in RNA biology, RNA-based therapeutics, RNA modifications/editing, epitranscriptomics, chromatin remodeling, mRNA-based therapeutics, drug discovery, drug delivery, biochemistry, chemical biology, development, epigenetics, immunology, tumor immunity, tumor microenvironment, pathology, metabolism, structural biology, and/or stem cell research. At least three years of highly productive postdoctoral research training experience. Preferred qualifications: Mouse model research experience is a plus. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . #PD United States-California-Monrovia", "summaryDescription" : "Staff Scientist - Cancer Research and RNA-Based Therapeutics at City of Hope", "createdAt" : "2026-06-14T21:52:39.491", "lastUpdated" : "2026-06-15T22:26:24.994", "ingestTimestamp" : "2026-06-14T21:52:39.491", "mongoId" : "6a0aaa1b1663d49372db0362", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 175000, "salaryAnnualMax" : 250000, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Lead", "dataQualityScore" : 0.7777778, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a3055f1f292fd229cf23389", "title" : "Support and Data Operations Associate (Fixed-term)", "company" : "Foursquare", "industry" : "Finance", "salary" : { "min" : 1000000.0, "max" : 1500000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Junior Support and Data Operations Associate in Belgrade, Serbia, adjusted for the technology industry and company size." }, "location" : "Serbia", "locations" : [ "Serbia" ], "certifications" : [ "GCP Professional Data Engineer", "AWS Data Analytics", "Databricks Certified", "Dbt Certified" ], "timestamp" : "2026-06-16T08:56:17.647", "fingerprint" : "aaf5559b6dd261874f5f77a1afd61a6fd75d245824898322671fec42e45798b8", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/foursquare/b98303fd-481a-4f08-9feb-451f7c9b179e/application", "externalId" : "b98303fd-481a-4f08-9feb-451f7c9b179e", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Belgrade", "country" : "Serbia", "continent" : "eu", "source" : "llm", "workMode" : "hybrid", "geo" : "44.8153318,20.4456588" } ], "locationText" : "Belgrade, Serbia", "employmentType" : "FULL_TIME", "technicalSkills" : "SQL, Python, R, Scala, Spark, Dbt, Tableau, Power BI, Looker, Metabase, Superset, Qlik, MicroStrategy, Snowflake, BigQuery, Redshift, Databricks, Fivetran, Airflow, Dbt Cloud, Delta Lake, Scikit-learn, TensorFlow, PyTorch, XGBoost, LightGBM, Hugging Face, MLflow, AWS, GCP, Azure, S3, Glue, SageMaker, Athena, Vertex AI, Synapse, ML Studio", "professionalSkills" : [ "Data engineering", "Machine learning", "Business intelligence", "Data analytics", "Quantitative analysis", "Data modelling" ], "hardSkillsList" : [ "Statistical methods", "ML frameworks", "BI platforms", "Cloud data stacks", "Modelling skills", "Regression", "Classification", "Clustering", "Time-series analysis", "A/B testing", "Causal inference" ], "hardSkills" : [ { "name" : "Statistical methods", "level" : "intermediate" }, { "name" : "ML frameworks", "level" : "intermediate" }, { "name" : "BI platforms", "level" : "intermediate" }, { "name" : "Cloud data stacks", "level" : "intermediate" }, { "name" : "Modelling skills", "level" : "intermediate" }, { "name" : "Regression", "level" : "intermediate" }, { "name" : "Classification", "level" : "intermediate" }, { "name" : "Clustering", "level" : "intermediate" }, { "name" : "Time-series analysis", "level" : "intermediate" }, { "name" : "A/B testing", "level" : "intermediate" }, { "name" : "Causal inference", "level" : "intermediate" } ], "majorSkills" : "Data science, Data engineering, Machine learning, Business intelligence", "majorSkillsList" : [ "Data science", "Data engineering", "Machine learning", "Business intelligence" ], "toolProficiency" : [ "SQL", "Python", "R", "Scala", "Spark", "Dbt", "Tableau", "Power BI", "Looker", "Metabase", "Superset", "Qlik", "MicroStrategy", "Snowflake", "BigQuery", "Redshift", "Databricks", "Fivetran", "Airflow", "Dbt Cloud", "Delta Lake", "Scikit-learn", "TensorFlow", "PyTorch", "XGBoost", "LightGBM", "Hugging Face", "MLflow", "AWS", "GCP", "Azure", "S3", "Glue", "SageMaker", "Athena", "Vertex AI", "Synapse", "ML Studio" ], "qualificationsBasic" : "SQL proficiency, 5+ years of experience", "qualificationsPreferred" : "PhD preferred, GCP Professional Data Engineer certification, AWS Data Analytics certification, Databricks Certified certification, Dbt Certified certification, Experience with scikit-learn, Experience with TensorFlow, Experience with PyTorch, Experience with XGBoost, Experience with LightGBM, Experience with Hugging Face, Experience with MLflow, Experience with Snowflake, Experience with BigQuery, Experience with Redshift, Experience with Databricks, Experience with dbt, Experience with Fivetran, Experience with Airflow, Experience with dbt Cloud, Experience with Delta Lake, Experience with AWS SageMaker, Experience with GCP Vertex AI, Experience with Azure ML Studio", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "About Foursquare Foursquare is the leading independent location technology and data cloud platform, helping businesses connect the digital and physical worlds with precision and purpose. Our products power everything from market analytics to targeted experiences, relied on by some of the world’s most iconic brands. But what makes Foursquare truly special is how we work. We're a team of builders, problem-solvers, and collaborators who care deeply about impact – both in the products we ship and the way we show up for each other. Great outcomes come from strong collaboration and shared ownership, and we believe growth happens through real challenges – whether that’s leveling up a skill, tackling unfamiliar problems, or pushing a project forward in a new way. If you're excited by cutting-edge tech and a culture that values both autonomy and teamwork, you’ll thrive here. About the Position Foursquare is looking for a Support and Data Operations Associate to join our team in our Belgrade office; on a hybrid schedule of Tuesday, Wednesday, Thursday in office. We are looking for an inquisitive, adaptable, and highly motivated Data Support Associate to join our team. In this role, you will be primarily focused on executing web crawls, manipulating data, and utilizing internal pipeline tools to ensure data quality and availability. This is an internally focused, highly technical role where persistence, vigilance, and the ability to learn and iterate quickly are essential. If you enjoy solving technical puzzles, building and maintaining data flows, and continuously learning new skills, we want you on our team! Please note that this is a fixed-term position for an initial period of one year, with the possibility of extension. In this role, you’ll - Web Crawling & Extraction: Execute and manage web crawling initiatives, extracting data, and adapting quickly when target site structures change. - Data Manipulation & Pipelines: Utilize internal tools to perform data cleanup, matching, and transformations to ensure high data quality and reliability. - Technical Troubleshooting: Be vigilant in monitoring data pipelines; investigate issues, read and interpret log files, implement workarounds, and escalate complex technical problems. - Continuous Improvement: Learn and adapt to new internal tools and technical processes rapidly, iterating on existing workflows to improve efficiency. - Documentation: Create and maintain technical process documentation and how-to guides to empower internal teams What you’ll need - Proficient level of written and verbal English - 1+ years of experience working in data-oriented customer operations, technical support, analytics, or similar roles. - Proficiency in Python or Scala, with strong SQL skills. - Proficiency in Regular Expressions (Regex) for pattern matching, data extraction, validation, and web content processing. - Familiarity with data analysis tools and libraries (e.g., PySpark, pandas), web crawling concepts and execution. - General technical troubleshooting skills: ability to read/interpret/transform log files, comfort navigating command-line interfaces (CLI) and APIs, and a strong capacity for independent research. - Your own unique talents! If you don’t meet 100% of the qualifications outlined above, we encourage and welcome you to still apply! Benefits and Perks - 25 days of paid vacation – take the time you need to rest and recharge - Private medical insurance – comprehensive coverage for you and your family - FitPass – flexible access to gyms, wellness classes, and sports facilities across Serbia - Hybrid work schedule – in-person collaboration Tuesday–Thursday, with company-paid lunch on office days - Growth Investment Program – funding and resources to support your personal and professional development - Tech setup – we’ll provide a company laptop and the essentials to help you get up and running smoothly Things to Know Foursquare is proud to foster an inclusive environment, free from discrimination. We believe that building the best products starts with bringing together diverse perspectives and backgrounds — it’s how we create better experiences for both our users and our team. We value every voice, and we encourage you to be part of building a company and products we love. Foursquare is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. Foursquare Privacy Policy https://location.foursquare.com/legal/privacy-center/applicant/", "summaryDescription" : "Support and Data Operations Associate (Fixed-term) at Foursquare. Skills: Data science, Data engineering, Machine learning, Business intelligence", "createdAt" : "2026-06-16T00:29:26.610", "lastUpdated" : "2026-06-16T08:56:17.647", "ingestTimestamp" : "2026-06-16T00:29:26.610", "mongoId" : "6a3055f1f292fd229cf23389", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Statistical methods", "ML frameworks", "BI platforms", "Cloud data stacks", "Modelling skills", "Regression", "Classification", "Clustering", "Time-series analysis", "A/B testing", "Causal inference", "Data science", "Data engineering", "Machine learning", "Business intelligence", "Data analytics", "Quantitative analysis", "Data modelling", "GCP Professional Data Engineer", "AWS Data Analytics", "Databricks Certified", "Dbt Certified", "SQL", "Python", "R", "Scala", "Spark", "Dbt", "Tableau", "Power BI", "Looker", "Metabase", "Superset", "Qlik", "MicroStrategy", "Snowflake", "BigQuery", "Redshift", "Databricks", "Fivetran", "Airflow", "Dbt Cloud", "Delta Lake", "Scikit-learn", "TensorFlow", "PyTorch", "XGBoost", "LightGBM", "Hugging Face", "MLflow", "AWS", "GCP", "Azure", "S3", "Glue", "SageMaker", "Athena", "Vertex AI", "Synapse", "ML Studio" ], "skillCount" : 60, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Junior", "dataQualityScore" : 0.7777778, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.95 }, { "id" : "6a30675bf292fd229cfbc0c1", "title" : "Current Intelligence and Operations Support Analyst 2", "company" : "Mobius", "salary" : { "min" : 105000.0, "max" : 145000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior, Mid-level Current Intelligence and Operations Support Analyst 2 in Fort Belvoir, United States, adjusted for government industry and company size." }, "location" : "Fort Belvoir, Virginia, United States", "locations" : [ "Fort Belvoir", "Virginia", "United States" ], "timestamp" : "2026-06-16T07:36:38.581", "fingerprint" : "204276798df96d65768dedd02ebb60b8286486eeb8c72469809de10a717a07f6", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://mobius-llc.com/careers?gh_jid=5165263007", "externalId" : "5165263007", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Fort Belvoir", "state" : "Virginia", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.7107970,-77.1436907" } ], "locationText" : "Fort Belvoir, Virginia, United States", "experienceMinYears" : 6, "experienceMaxYears" : 10, "experienceLevel" : "Mid", "rawDescription" : "Mobius is an award winning, Small Business Administration (SBA) certified Historically Underutilized Business Zone (HUBZone) company and certified Woman-Owned Small Business (WOSB) providing engineering, analytical, and programmatic expertise to the Federal Government and commercial customers. Our mission is to provide innovative advanced technology solutions to customers facing issues of national and global significance. We strive to be admired for excellent people, fair and honest partnership, innovative problem solving, and exceptional performance. Come join our team! Mobius is seeking a Current Intelligence and Operations Support Analyst 2. In this role you will provide support to the MDA Executives, Program Elements, and other Agency two letter organizations, which includes meetings, one-on-one discussions, briefings and other daily interactions with senior leaders, Program Elements, and other MDA two letter organizations, preparation and delivery of daily intelligence products to include an SCI-level Daily Read Book, interacting with senior IC leaders and analysts to coordinate and acquire information and then provide quick or immediate responses to queries from senior leadership, and responding to requests for information (RFIs), and supporting the development of all Intelligence Division Current Intelligence products. This position is located at Ft Belvoir, VA. Duties of a Current Intelligence and Operations Support Analyst 2 may include: Perform technical intelligence analyses Develop and deliver special studies, briefings, papers, executive correspondence, and reports Interact with IC senior leaders and analysts to acquire the intelligence required to respond to RFIs and inquiries from across MDA Research, write, and publish daily, weekly, and monthly current intelligence products for distribution to MDA customers Identify and post relevant content to the Missile Intelligence Secure Link (MISL) portal site Produce ad hoc threat topic intelligence documents such as reports, white papers, technical data, briefings, and assessments Plan and organize meetings, conferences and symposia, as directed by Intelligence Division Government staff Qualifications 6-10 years’ experience in intelligence analysis Can execute analytical tasks, utilizing both analytical techniques, and processes Able to develop and/or utilize analytic tools, techniques, and processes for technical and/or administrative support activities Can work independently and/or leads teams to analyze and resolve problems Can apply oral and written communication skills Must be able to provide daily supervision and direction to support teams Degree in relevant fields such as history, political science, sociology, or another social science field Education Degree in relevant fields such as history, political science, sociology, or another social science field Clearance Active Top Secret clearance with SCI eligibility Mobius Benefits: Mobius offers a stable work environment, a competitive salary, and a comprehensive benefits package, which includes medical, dental and vision plans, 401k Plan, Flexible Work Schedules, Tuition Reimbursement, Paid Leave and much more. Mobius is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity Employer/Affirmative Action Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class.", "summaryDescription" : "Current Intelligence and Operations Support Analyst 2 at Mobius", "postedDate" : "2026-06-15T23:25:01.552", "createdAt" : "2026-06-15T23:25:01.552", "lastUpdated" : "2026-06-16T07:36:38.581", "ingestTimestamp" : "2026-06-15T23:25:01.552", "mongoId" : "6a30675bf292fd229cfbc0c1", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 105000, "salaryAnnualMax" : 145000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "data", "seniorityLevel" : "Senior", "dataQualityScore" : 0.7777778, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Government", "llmIndustryConfidence" : 0.95 }, { "id" : "6a1683dd58b93c861eae69cb", "title" : "Voice and Chat Customer Support", "company" : "Support Services Group", "salary" : { "min" : 1080000.0, "max" : 1560000.0, "currency" : "JMD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Entry-level voice and chat customer support roles in Kingston, Jamaica, typically range from JMD 1,080,000 to JMD 1,560,000 annually, based on 2024-2025 market data for the customer support industry." }, "location" : "Kingston, JM", "locations" : [ "Kingston", "JM" ], "timestamp" : "2026-06-15T22:52:29.391", "fingerprint" : "4f6ae0e296beb50910f2a62d0981c4c812e73f3e568ae5acf3f7d6192512de0d", "source" : "breezyhr", "language" : "en", "applyUrl" : "https://ssg-corp.breezy.hr/p/134045a3cb25-voice-and-chat-customer-support", "externalId" : "134045a3cb25", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Kingston", "state" : "Saint Andrew", "country" : "Jamaica", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "17.9841723,-76.8057525" } ], "locationText" : "Kingston, Saint Andrew, Jamaica", "employmentType" : "FULL_TIME", "coreResponsibilities" : "Field customer inquiries, Address customer pain points, Maintain product knowledge", "outcomesObjectives" : "Drive customer satisfaction", "qualificationsBasic" : "Extensive product knowledge", "workSiteFlexibility" : "Onsite", "rawDescription" : "Support Services Group is looking for customer service representatives to join our team in our Kingston, Jamaica office. This person will drive customer satisfaction by fielding inquiries, addressing pain points, and maintaining extensive product knowledge. This role would include email, voice and", "summaryDescription" : "Voice and Chat Customer Support at Support Services Group. Field customer inquiries. Address customer pain points", "createdAt" : "2026-06-14T21:53:59.292", "lastUpdated" : "2026-06-15T22:52:29.391", "ingestTimestamp" : "2026-06-14T21:53:59.292", "mongoId" : "6a1683dd58b93c861eae69cb", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "sales", "jobSubcategory" : "customer_success", "seniorityLevel" : "Entry", "dataQualityScore" : 0.6666667, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Customer Support", "llmIndustryConfidence" : 0.95 }, { "id" : "6a3057b0f292fd229cf3d1ad", "title" : "Model-Based Systems Engineer", "company" : "STR", "salary" : { "min" : 125000.0, "max" : 175000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Mid-level Model-Based Systems Engineer in Arlington, United States, adjusted for the technology industry and company size." }, "location" : "Arlington, Virginia, United States", "locations" : [ "Arlington", "Virginia", "United States", "Dayton", "Ohio", "United States", "Woburn", "Massachusetts", "United States" ], "timestamp" : "2026-06-16T08:27:42.989", "fingerprint" : "4c6e54a66b20b9ef01387c586df853cc9587bf0075fa02b8d86b7bd5d687c7e9", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/systemstechnologyresearch/jobs/4688995006", "externalId" : "4688995006", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Arlington", "state" : "Virginia", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "38.8769326,-77.0893094" } ], "locationText" : "Arlington, Virginia, United States", "rawDescription" : "STR is hiring a Model-Based Systems Engineer (MBSE) to work across a broad portfolio of DoD mission areas. The Systems Engineer should have experience architecting systems, working across the Systems Engineering Lifecycle, a deep understanding of Systems Engineering principles, reverse engineering techniques, and the ability to work with complex software systems and the utilization of Digital Engineering/MBSE to accomplish program goals. The candidate will support STR’s Systems Development Division to achieve architectural integrity and traceability from requirements analysis through system and software development and production system deployment. This position offers the opportunity to work with leading domain experts developing solutions to solve the most challenging national security problems. Our teams consist of motivated individuals with degrees in engineering, computer science, mathematics, physics, and data science. The ideal candidate will be experienced in Systems Engineering processes and techniques, Modeling and Simulation, software-based systems, Digital Engineering/MBSE and be excited about opportunities to grow and be a source of subject matter expertise across the organization. The Systems Engineer should have experience implementing a rigorous MBSE approach to develop DoD systems. New programs at STR will be looking to adopt agile approaches that incorporate model-based requirements management and traceability with software development. This position is well suited for a Systems Engineer with a software systems background who is interested in improving the state of the practice and demonstrating the advantages that MBSE can offer. What you will do: Utilize your Systems Engineering skillset as part of a tightly knit team to design, develop, implement, and deploy advanced software systems Analyze, reverse-engineer, derive, and define requirements from ambiguous or incomplete software system implementations and codebases Develop/generate documentation (e. g. Systems Requirements Document, SysML models) to capture requirements of new and existing systems Perform gap analysis between derived requirements and current system capabilities to identify missing features or functionalities Assist other technical contributors throughout the software lifecycle, from early prototypes to fully integrated systems Implement MBSE approaches using SysML in Cameo Work closely with domain experts and software development teams to realize program designs for a diverse set of applications, including: Distributed mission planning Intelligence Surveillance Reconnaissance (ISR) management Decision making support to human analysts/planners This position is based in one of our offices but will take advantage of STR’s flexible, hybrid environment: we anticipate that you could work remotely as much as 25% of the time Any time work does not require use of STR’s facilities, you are welcome to work remotely Who you are: This position requires an Active DoD Top Secret Clearance with SCI eligibility, for which U. S. citizenship is needed by U. S. Government BS, MS or PhD in Systems Engineering, Computer Science, Aerospace Engineering, Electrical Engineering, or a related technical field Experience implementing open architectures and integrating with large scale software-intensive systems and platform systems Strong ability to derive requirements from existing software and capture new customer requirements, and translate those into development tasks for software teams Comfortable working in dynamic environments and adjusting to changing priorities Minimum of 2 years work experience as a Systems Engineer or related field Experience architecting systems using system modeling tools (SysML in Cameo) Even Better: Domain expertise or familiarity with one or more of the following areas is highly desirable: Sea, air, and space platforms, mission planning, and C2 systems Sensor Resource Management Electronic Warfare Software deployment in cloud-based systems Government Open System Architectures (UCI, OMS, COARPS) 5+ years of experience in architecting systems using system modeling tools (SysML in Cameo) Experience porting models/designs from SparxEA to Cameo Experience in Java, Python, or object-oriented programming languages Agile software development experience and/or certification Pay Information Full-Time Salary Range: $110,000 - $150,000 The salary range listed is based on external market data. Offers are based on factors, such as but not limited to, the candidate’s experience, education, training, key skills/critical skills, security clearances, and prevailing market and business conditions. STR is a growing technology company with locations near Boston, MA, Arlington, VA, near Dayton, OH, Melbourne, FL, and Carlsbad, CA. We specialize in advanced research and development for defense, intelligence, and national security in: cyber; next generation sensors, radar, sonar, communications, and electronic warfare; and artificial intelligence algorithms and analytics to make sense of the complexity that is exploding around us. STR is committed to creating a collaborative learning environment that supports deep technical understanding and recognizes the contributions and achievements of all team members. Our work is challenging, and we go home at night knowing that we pushed the envelope of technology and made the world safer. STR is not just any company. Our people, culture, and attitude along with their unique set of skills, experiences, and perspectives put us on a trajectory to change the world. We can't do it alone, though - we need fellow trailblazers. If you are one, join our team and help to keep our society safe! Visit us at www.str.us for more info. STR is an equal opportunity employer. We are fully dedicated to hiring the most qualified candidate regardless of race, color, religion, sex (including gender identity, sexual orientation and pregnancy), marital status, national origin, age, veteran status, disability, genetic information or any other characteristic protected by federal, state or local laws. If you need a reasonable accommodation for any portion of the employment process, email us at appassist@str.us and provide your contact info. Pursuant to applicable federal law and regulations, positions at STR require employees to obtain national security clearances and satisfy the requirements for compliance with export control and other applicable laws.", "summaryDescription" : "Model-Based Systems Engineer at STR", "postedDate" : "2026-06-15T23:22:53.102", "createdAt" : "2026-06-15T23:22:53.102", "lastUpdated" : "2026-06-16T08:27:42.989", "ingestTimestamp" : "2026-06-15T23:22:53.102", "mongoId" : "6a3057b0f292fd229cf3d1ad", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 125000, "salaryAnnualMax" : 175000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.98 }, { "id" : "6a305649f292fd229cf26cd7", "title" : "Software Development Engineer, Lead Management and Account-Based Marketing", "company" : "Amazon Web Services, Inc.", "industry" : "Marketing PR, Software Development, Cloud Computing", "salary" : { "min" : 143700.0, "max" : 194400.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Seattle, Washington, USA", "locations" : [ "Seattle, Washington, USA" ], "timestamp" : "2026-06-16T07:21:35.585", "fingerprint" : "9fa849a98073c2db7e70d00d1a9c943edffdeab94c9a9c195339d5f436224569", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.jobs/jobs/10449074/apply", "externalId" : "14d70e22-ebf5-4491-a002-2a0f4df9244f", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Seattle", "state" : "Washington", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "47.6038321,-122.3300620" } ], "locationText" : "Seattle, Washington, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 8, "experienceMaxYears" : 15, "experienceLevel" : "Lead", "remoteFriendly" : false, "workSiteFlexibility" : "onsite", "rawDescription" : "Sales, Marketing and Global Services (SMGS) AWS Sales, Marketing, and Global Services (SMGS) is responsible for driving revenue, adoption, and growth from the largest and fastest growing small- and mid-market accounts to enterprise-level customers including public sector. The AWS Global Support team interacts with leading companies and believes that world-class support is critical to customer success. AWS Support also partners with a global list of customers that are building mission-critical applications on top of AWS services. The core mission of AWS Marketing is to educate customers about cloud computing and our services. As a fast growing business, we get thousands of leads via events, webinars, website, and campaigns that we process, score, and pass the highest quality leads to our sales teams. Imagine building a platform that that will be built using AWS technologies to store millions of customer lead records, continuously keep their attributes updated based on factors like their demographics, marketing activities they engage with, products they show interest etc. Imagine working with global AWS Marketing and Sales leaders to understand the AWS buying process and building the engine that enables that end to end from ingesting leads to sending to Sales follow-up and then also building the feedback mechanism on performance. You and your team will build various modules which will be responsible for ingesting leads, enriching them with attributes that we gather from 3rd party and 1st party data, scoring the leads, and handing the highest quality leads to appropriate sales teams. Interested in diving in? As Software Development Engineer for the AWS Lead Management and Account-Based Marketing Engineering team, you will join a fast growing tech organization with plenty of technical talent. You will develop a high quality, creative, technology platform that powers ingesting and passing along the highest quality leads to the AWS Sales teams. Your team will drive and own core innovations for our customers worldwide. You will closely interact with senior managers and stakeholders on a global scale, prioritizing and autonomously driving the full software development lifecycle for your team. You will work on critical projects that significantly contribute to the significant growth of AWS. You will make a huge, measurable impact to the AWS buying and lead management process, and build and innovate solutions that are simple and easy to maintain and scale. You are a strong technical leader. You are great at hiring, growing, and mentoring engineers, and at cultivating leadership capabilities. Are you an experienced software development leader, ready to challenge yourself to work hard, have fun, and make history with AWS? Come and join the AWS Marketing Lead Management team! Key job responsibilities - Implementation of a scalable E2E technical design across all systems in the solution - AWS tools, API, Redshift - Deliver validated conceptual architecture - Write and prioritize architectural enablement work items - Evaluates technical feasibility of features - Defines migration plan from current to future state - Defines environment setup and continuous integration/continuous delivery standards A day in the life The ideal candidate will have a track record of success, delivering new features or products. This person has thrived on delivering high quality technology products/services in a hyper-growth environment where priorities shift fast. They have strong design and implementation experience, digs deep into data, has a strong knowledge of web services and protocols, and an in-depth knowledge of distributed systems architectures and integration between third party applications. About the team Diverse Experiences Amazon values diverse experiences. Even if you do not meet all of the preferred qualifications and skills listed in the job description, we encourage candidates to apply. If your career is just starting, hasn’t followed a traditional path, or includes alternative experiences, don’t let it stop you from applying. Why AWS Amazon Web Services (AWS) is the world’s most comprehensive and broadly adopted cloud platform. We pioneered cloud computing and never stopped innovating — that’s why customers from the most successful startups to Global 500 companies trust our robust suite of products and services to power their businesses. Work/Life Balance We value work-life harmony. Achieving success at work should never come at the expense of sacrifices at home, which is why flexible work hours and arrangements are part of our culture. When we feel supported in the workplace and at home, there’s nothing we can’t achieve in the cloud. Inclusive Team Culture Here at AWS, it’s in our nature to learn and be curious. Our employee-led affinity groups foster a culture of inclusion that empower us to be proud of our differences. Mentorship and Career Growth We’re continuously raising our performance bar as we strive to become Earth’s Best Employer. That’s why you’ll find endless knowledge-sharing, mentorship and other career-advancing resources here to help you develop into a better-rounded professional. Basic Qualifications: - 3+ years of non-internship professional software development experience - 2+ years of non-internship design or architecture (design patterns, reliability and scaling) of new and existing systems experience - 1+ years of software development engineer or related occupational experience - 1+ years of designing and developing large-scale, multi-tiered, multi-threaded, embedded or distributed software applications, tools, systems, and services using: C#, C++, Java, or Perl experience - 1+ years of Object Oriented Design experience - Bachelor's degree or foreign equivalent in Computer Science, Engineering, Mathematics, or a related field - Experience programming with at least one software programming language Preferred Qualifications: - 3+ years of full software development life cycle, including coding standards, code reviews, source control management, build processes, testing, and operations experience - Bachelor's degree in computer science or equivalent Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner. The base salary range for this position is listed below. Your Amazon package will include sign-on payments and restricted stock units (RSUs). Final compensation will be determined based on factors including experience, qualifications, and location. Amazon also offers comprehensive benefits including health insurance (medical, dental, vision, prescription, Basic Life & AD&D insurance and option for Supplemental life plans, EAP, Mental Health Support, Medical Advice Line, Flexible Spending Accounts, Adoption and Surrogacy Reimbursement coverage), 401(k) matching, paid time off, and parental leave. Learn more about our benefits at https://amazon.jobs/en/benefits . USA, WA, Seattle - 143,700.00 - 194,400.00 USD annually", "summaryDescription" : "Software Development Engineer, Lead Management and Account-Based Marketing at Amazon Web Services, Inc.", "postedDate" : "2026-06-15T00:00:00.000", "createdAt" : "2026-06-15T22:01:33.321", "lastUpdated" : "2026-06-16T07:21:35.585", "ingestTimestamp" : "2026-06-15T22:01:33.321", "mongoId" : "6a305649f292fd229cf26cd7", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.jobs/jobs/10449074/apply", "salaryAnnualMin" : 143700, "salaryAnnualMax" : 194400, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Lead", "dataQualityScore" : 0.8888889, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2d0d3e74d8ee00a0ad3169", "title" : "RBT School Based", "company" : "BAYADA Home Health Care", "industry" : "Healthcare", "salary" : { "min" : 30.0, "max" : 35.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Behavioral Health - Field", "locations" : [ "Behavioral Health - Field", "Field" ], "timestamp" : "2026-06-15T22:30:52.434", "fingerprint" : "7ca7d41080055bf1712620d368504aa422efb75b926e44ee45260502efe78c14", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/bayada/jobs/8590577002", "externalId" : "8590577002", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Honolulu", "state" : "Hawaii", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "21.3045470,-157.8556760" }, { "city" : "Honolulu", "state" : "Hawaii", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "21.3045470,-157.8556760" }, { "city" : "Honolulu", "state" : "Hawaii", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "21.3045470,-157.8556760" }, { "city" : "Honolulu", "state" : "Hawaii", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "21.3045470,-157.8556760" }, { "city" : "Honolulu", "state" : "Hawaii", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "21.3045470,-157.8556760" }, { "city" : "Honolulu", "state" : "Hawaii", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "21.3045470,-157.8556760" }, { "city" : "Honolulu", "state" : "Hawaii", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "21.3045470,-157.8556760" }, { "city" : "Honolulu", "state" : "Hawaii", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "21.3045470,-157.8556760" }, { "city" : "Honolulu", "state" : "Hawaii", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "21.3045470,-157.8556760" } ], "locationText" : "Honolulu, Hawaii, United States; Honolulu, Hawaii, United States; Honolulu, Hawaii, United States; Honolulu, Hawaii, United States; Honolulu, Hawaii, United States; Honolulu, Hawaii, United States; Honolulu, Hawaii, United States; Honolulu, Hawaii, United States; Honolulu, Hawaii, United States", "employmentType" : "FULL_TIME", "remoteFriendly" : false, "rawDescription" : "Are you interested in supporting children with autism to reach their fullest potential? Then this is the position for you! At BAYADA Home Health Care, our clients come first and our employees are our greatest asset. We are looking for dedicated employees who have their Registered Behavior Technician (RBT) credential or are interested in pursuing their Registered Behavior Technician (RBT) credential. The RBT credential is a professional credential for paraprofessionals offered through the Behavior Analyst Certification Board (BACB). The RBT credential is required for individuals providing services on any Applied Behavior Analysis (ABA) or insurance-based contracts in Hawaii. This position includes working 1:1 in the home and community with children and young adults diagnosed with autism. BAYADA will pay for your training as well as provide extensive supervision. Sign On Bonus: $1500 We have current Registered Behavior Technician (RBT) openings in the following locations: Honolulu Ala Moana Waikiki Hawaii Kai Kalihi Manoa Aiea Salt Lake Pearl Harbor Schedule: Monday through Friday Time (7:30am- 3pm) BAYADA Offers Registered Behavior Technicians (RBTs): Health Insurance Paid Time Off Scholarships Employee Appreciation Events Weekly Pay Schedule Qualifications for Registered Behavior Technician (RBT): One year experience working with children with developmental/ intellectual disabilities preferred Responsibilities for Registered Behavior Technician (RBT): Work directly with clients and follow the established treatment plan/behavior support plan for implementing skill acquisition and behavior reduction procedures. Establish and maintain effective, supportive, and therapeutic relationships with clients & families. Respect the values, thoughts, beliefs, and attitudes of clients and families. Implement behavior therapy techniques as instructed by the Behavioral Services Manager and Behavior Specialist. Document interventions and progress towards goals accurately and in a timely manner. Collect behavior data as specified in client behavior support plan. Review data and progress reports with Behavioral Services Manager and Behavior Specialist in order to strategize program improvements. As applicable to the treatment plan, provide habilitation, training, instruction, and assistance to help the client acquire and maintain skills and to help meet identified goals. As applicable, provide transportation related to the implementation of activities as directed by the treatment plan. Provide training and/or support to the client in interpersonal skills, the development and maintenance of personal relationships, and in living in his/her community. Monitor health status and physical condition and reports any changes in the client’s condition or other incidents to the office. BAYADA recognizes and rewards our RBTs who set and maintain the highest standards of excellence. Join our caring team today! Starting Pay Range: $30-$35/hr As an accredited, regulated, certified, and licensed home health care provider, BAYADA complies with all state/local mandates. BAYADA is celebrating 50 years of compassion, excellence, and reliability. Learn more about our 50th anniversary celebration and how you can join in here. BAYADA Home Health Care, Inc., and its associated entities and joint venture partners, are Equal Opportunity Employers. All employment decisions are made on a non-discriminatory basis without regard to sex, race, color, age, disability, pregnancy or maternity, sexual orientation, gender identity, citizenship status, military status, or any other similarly protected status in accordance with federal, state and local laws. 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What: Hiring an experienced, customer-focused professional to provide advanced support and operational leadership through troubleshooting, workflow oversight, training support, special project execution, and more across HealtheConnections’ technology services. About the Job: In this role, you will use your experience and critical thinking skills to work closely with customers to understand their needs, provide guidance on our systems and services, manage important processes, and serve as a trusted resource. This team supports one of the largest and most multi-faceted health information exchanges in the country and serves as a key resource for both customers and internal teams. Administrative and Customer Support Specialists have varied responsibilities. You will work closely with customers and team members to ensure a high-quality customer experience while supporting onboarding, compliance, customer service operations, and continuous improvement initiatives. Primary Responsibilities: Serve as a primary point of contact for customer inquiries, service requests, and support issues, delivering an exceptional customer experience through phone, email, and tickets Be a subject matter expert for Customer Services processes and how HealtheConnections’ services work. Troubleshoot and resolve complex customer issues while ensuring timely follow-up and resolution. Support the categorization, triage, escalation, and management of customer support tickets using our CRM and other business systems Maintain accurate customer records, user accounts, and system documentation. Support customer onboarding, credentialing, compliance, and customer experience initiatives. Experience Needed: Please send us a cover letter with your application. 5+ years of customer service, customer support, client services, or related experience. Experience with CRM, ticketing, or customer support platforms. Excellent written and verbal communication skills. Strong analytical and problem-solving abilities. Strong technical aptitude and ability to quickly learn new applications and systems. Ability to work under pressure, meet deadlines, and ensure accuracy. Proven ability to follow established procedures. Experience working independently and collaboratively within a team environment. Experience in healthcare, health information exchange, health IT, medical administration, or a technical support environment is a strong plus. Associate's or higher degree in Business, Communications, Healthcare Administration, Information Technology, or equivalent experience strongly preferred Not sure you meet all qualifications? Research shows that women and members of other under-represented groups tend to not apply to jobs when they think they may not meet every qualification, when, in fact, they do! We are committed to creating a diverse and inclusive environment and strongly encourage you to apply. You’re a great fit for us if you’re good at… Methodical, detail-oriented tasks Being flexible and adaptable to shifting priorities Following procedures carefully Helping someone get to the root of a problem We’re a great fit for you if you’re looking for… A high-performance, high-energy, collaborative environment. One of the best things about working here is our team. They’re smart, supportive, passionate, and among the best in the business. A dynamic industry. Health information exchange has exciting opportunities on the horizon as the healthcare industry evolves, both within NYS and on the national stage. Strong benefits. We cover the cost of medical insurance for employees along with a full suite of benefits, including 401k matching, generous vacation/holiday time, unlimited sick time, flexibility in work hours and hybrid/remote work, and more. Work that makes a difference in your community. We’re proud to make an impact on the daily lives of health professionals and support improved health outcomes for individuals right here in New York State. We like to say that we’re “casually competent” – we’re not pretentious, but we know our stuff. Our people are talented, our culture is vibrant, and our work is at the top of its class. Even better, our customers genuinely like working with us, and we’ve seen firsthand how what we do has made a positive impact on our community. $48,000-$62,500 is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. We may ultimately pay more or less than the posted range, and the range may be modified in the future. 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We’re growing rapidly and are hiring for talented people to scale and support the massive demand for AI-driven wet lab experimentation. ABOUT THE ROLE You'll build out protein expression and purification at Adaptyv, with a focus on mammalian systems — CHO and HEK, transient and stable. This is the foundation the rest of the platform stands on: titers, quality, and turnaround here set the ceiling for everything downstream. Your job is to take expression and purification from bespoke, person-dependent protocols to a robust, automated, high-throughput product. You'll optimize and run the science hands-on, work with lab automation to scale it onto liquid handlers and automated systems, and work with the software team to track samples, capture process data, and make production observable and predictable. You'll lead the science and stay deeply hands-on. WHAT YOU'LL DO - Develop, optimize, and run mammalian expression hands-on (CHO/HEK, transient and stable), pushing titer, quality, and reproducibility. - Own purification across modalities (Protein A, IEX, SEC, and related) and the quality of the proteins we ship. - Turn expression and purification into a productized, high-throughput, automated capability with predictable turnaround. - Partner with lab automation to scale workflows onto automated systems, and reduce manual, person-dependent steps. - Work with the software team to track samples and process parameters, and make production yields and quality observable and improvable. - Set the quality bar and troubleshoot the inevitable failures across biology, reagents, and process. WHAT WE'RE LOOKING FOR - Deep, hands-on expertise in mammalian protein expression and purification — CHO/HEK, and the full path from construct to purified, characterized protein. - Applied industry experience. 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TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

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We're entering the era of agentic science where AI models can now design novel proteins, propose hypotheses, and iterate on experimental results. But they can't run the experiments themselves - that's still a manual, months-long process. We're building the infrastructure that gives AI agents access to the physical world. We are one of Europe’s fastest-growing biotech startups, trusted by leading biopharmas, frontier AI labs, and the techbio companies pushing the field forward. This is a rare chance to help advance some of the most important work happening in biotech today. Our automated lab is powered by a deep software + hardware stack: lab instruments worth millions of USD reverse-engineered into API-controllable hardware, dozens of devices orchestrated through complex workflows, full observability on everything that happens in the lab, processing pipelines for messy physical-world data, and AI systems that troubleshoot production results and accelerate assay development. We’re growing rapidly and are hiring for talented people to scale and support the massive demand for AI-driven wet lab experimentation. RESPONSIBILITIES - Run and benchmark open-source protein design methods on real Adaptyv targets, validated against experimental data from our wet lab. - Design binders for internal R&D campaigns, and track experimental performance across success rate, hit rate, kinetics, and developability. - Build computational tooling around the design pipeline: structure prediction, filtering, and ranking, to triage large design pools down to candidates for synthesis and characterization. - Support the technical side of our open competitions and hackathons: drafting track briefs, supporting participants, judging submissions, and writing up results. - Contribute open data, blog posts, designer spotlights, and method comparisons to Proteinbase. QUALIFICATIONS - Currently enrolled in a Master's, PhD, or final-year undergraduate programme in computational biology, machine learning, biochemistry, biophysics, bioengineering, or a related field. - Hands-on experience with at least one modern open-source protein design method. - Strong Python and PyTorch skills. Comfortable working with biology data formats. - A working understanding of binding kinetics and developability that extends beyond in silico metrics, with a healthy scepticism of computational scores as ground truth. - Bonus: prior open-source contributions to a protein design repository, a strong showing in a public design competition, or a published blog post or paper. Duration: 3-6 months. Paid. Location: Remote, or on-site in Lausanne. Lausanne is preferred if you want lab access and the full design-build-test-learn exposure. Application deadline We are reviewing applicants on a rolling basis. Please include a link to a GitHub repository, competition submission, blog post, or other concrete work demonstrating your approach to protein design. Application deadline We are reviewing applicants on a rolling basis.", "summaryDescription" : "Intern, Protein Design at Adaptyv. Skills: Protein design, Machine learning, Computational biology. Run and benchmark protein design methods. 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Work with internal stakeholders", "projectManagementSkills" : [ "Prioritizing work", "Manage multiple projects" ], "domainKnowledge" : "Protein degradation; Cancer diseases; Inflammatory diseases; Structural studies; Functional studies", "domainList" : [ "protein-degradation", "cancer-diseases", "inflammatory-diseases", "structural-studies", "functional-studies" ], "domainSpecificKnowledge" : [ "Protein degradation", "Cancer diseases", "Inflammatory diseases", "Structural studies", "Functional studies" ], "toolProficiency" : [ "Electronic lab notebook" ], "documentationSkills" : "Record keeping", "problemSolvingSkills" : "Troubleshooting", "specialRequirements" : "Onsite role", "qualificationsBasic" : "MS or equivalent with 2+ years experience, 2+ years experience with insect cell lines, 2+ years experience with baculovirus expression, Maintain insect cell cultures, Maintain mammalian cell cultures, Lift 50+ pounds comfortably", "qualificationsPreferred" : "Ph.D., Experience with recombinant protein expression in mammalian cells, Overexpress milligram amounts of protein, Familiarity with multiplexed/automated microscale purification technologies, Experience expressing multi-subunit protein complexes, Troubleshoot difficult protein expressions, Purifying recombinant proteins", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Company Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix’s dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine’s next chapter with a new script to outmatch disease. Position Summary: Research Associate III – Scientist I Protein Expression Contractor Nurix Therapeutics, Inc. is seeking a detail-oriented and experienced Protein Expression Research Associate Contractor to join the DEL and Protein Sciences team. This individual will work cross functionally with internal stakeholders to plan, coordinate, and execute all operational activities required for analytical scale and preparative scale expression of recombinant proteins in baculovirus and mammalian cell systems. Additionally, they will be responsible for documentation of expression conditions and results in internal databases and electronic lab notebook systems. This is an onsite role. Qualifications MS or equivalent with 2+ years of relevant experience, or Ph. D. This position requires 2+ years of experience working with insect cell lines and baculovirus expression of recombinant proteins. Additional experience working with recombinant protein expression in mammalian cells (e. g. HEK293) is a plus. Industry experience preferred with exemplified ability to overexpress milligram amounts of protein for structural and functional studies for multiple protein classes. Highly proficient in maintaining insect cell and mammalian cell cultures. Excellent knowledge and high degree of familiarity with all steps in baculovirus expression of recombinant proteins, including clone design, generation and purification of bacmids, raising and titering of baculovirus, conducting MOI studies, cell culture of Sf9 and/or Tni/Hi5 cells, and harvesting of biomass on the scale of 1 L – 20 L. Strong working knowledge of protein characterization steps, including SDS-PAGE analysis, size exclusion chromatography, and/or thermal stability (e. g. nanoDSF). Must be able to lift 50+ pounds comfortably. Familiarity with multiplexed/automated microscale purification technologies (e. g. magnetic beads) is desirable. Previous experience expressing multi-subunit protein complexes is a plus. Past experience troubleshooting difficult protein expressions for a variety of target proteins is a plus. Past experience purifying recombinant proteins (e. g. affinity chromatography, ion exchange, or size exclusion chromatography) is a bonus. Able to work in dynamic, fast-paced environment with experience prioritizing work across multiple projects. Detail-oriented with strong record keeping skills. Fit with Nurix Culture Strong communication skills and an effective team player. A respectful lab citizen who maintains an organized and clean working environment. Intellectually curious and highly motivated to learn. Salary Range (based on experience): RA III $56- $64 per hour SRA $70 - $81 per hour Scientist I $76 - $86 per hour Location Brisbane, CA - Onsite Nurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. 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TGH Main Campus (TGHMAIN)
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Skills: Data center operations, Hardware support. Install and configure servers. Perform hardware maintenance", "postedDate" : "2026-06-16T01:52:20.705", "createdAt" : "2026-06-16T01:52:20.705", "lastUpdated" : "2026-06-16T13:54:09.956", "ingestTimestamp" : "2026-06-16T01:52:20.705", "mongoId" : "6a307f1ff292fd229c0556cd", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 70000, "salaryAnnualMax" : 95000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Hardware installation", "Cable management", "Rack and stack", "Data center operations", "Hardware support", "Public sector IT", "CompTIA A+", "Ticketing systems" ], "skillCount" : 8, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 0.5555556, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.9 }, { "id" : "6a17673d58b93c861ee3078b", "title" : "Clinical Nurse Manager- Surgical Trauma ICU Step Down", "company" : "Tampa General Hospital", "industry" : "Healthcare", "salary" : { "min" : 115000.0, "max" : 165000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Manager-level Clinical Nurse Manager- Surgical Trauma ICU Step Down in Tampa, United States, adjusted for industry and company size." }, "location" : "United States-Florida-Tampa", "locations" : [ "United States-Florida-Tampa", "
TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

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May be called on to deliver nursing care to patients on assigned unit according to established nursing standards, policies, procedures, and professional guidelines. Responsible to assist with daily clinical operations and assists with the, quality/safety, patient experience, financial management of the assigned unit. Assists in interviews and makes hiring decisions as required. Assigns work to and participates in the evaluation of the employees supervised. Responsible for performing job duties in accordance with mission, vision and values of Tampa General Hospital. Required Skills Current license to practice as a Registered Nurse in Florida. Graduate of an accredited School of Nursing. Bachelor’s of Science in Nursing (BSN) required. Minimum of two years of experience as an R.N. required. Tampa", "summaryDescription" : "Clinical Nurse Manager- Surgical Trauma ICU Step Down at Tampa General Hospital. Skills: Surgical Trauma ICU, Step Down Care, Nursing Management. Provide clinical support. Provide administrative support", "createdAt" : "2026-06-14T08:46:24.677", "lastUpdated" : "2026-06-15T08:37:31.369", "ingestTimestamp" : "2026-06-14T08:46:24.677", "mongoId" : "6a17673d58b93c861ee3078b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 115000, "salaryAnnualMax" : 165000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Nursing care delivery", "Surgical Trauma ICU", "Step Down Care", "Nursing Management", "Clinical operations", "Quality management", "Safety management", "Patient experience", "Financial management", "Step Down Unit", "Registered Nurse license in Florida" ], "skillCount" : 11, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Manager", "dataQualityScore" : 0.7777778, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c903c74d8ee00a097fb1c", "title" : "Center-Based Behavior Technician", "company" : "Centria Autism", "industry" : "Healthcare", "salary" : { "min" : 18.0, "max" : 24.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Phoenix, Arizona, United States", "locations" : [ "Phoenix", "Arizona", "United States" ], "certifications" : [ "Registered Behavior Technician (RBT)" ], "timestamp" : "2026-06-16T02:57:35.510", "fingerprint" : "883b14421eebd6b0536bc5b5a2d9c0200f4df5fe398ce3aaf9e13fb2fc090f86", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/centriaautism/jobs/8586583002", "externalId" : "8586583002", "industryFunction" : { }, "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", "professionalSkills" : [ "Behavioral analysis", "Data collection", "Intervention implementation" ], "majorSkills" : "Behavioral Technician, ABA Therapy", "majorSkillsList" : [ "Behavioral Technician", "ABA Therapy" ], "coreResponsibilities" : "Implement behavior intervention plans, Collect data on client progress, Provide direct therapy to clients, Assist with client assessments, Maintain client records, Communicate with supervisors and team members, Ensure client safety, Follow ethical guidelines", "teamCollaboration" : "Supervisors; Team members", "domainKnowledge" : "Autism Spectrum Disorder; Behavioral therapy principles", "domainList" : [ "autism-spectrum-disorder", "behavioral-therapy-principles" ], "domainSpecificKnowledge" : [ "Autism Spectrum Disorder", "Behavioral therapy principles" ], "toolProficiency" : [ "EHR systems" ], "documentationSkills" : "Client records", "specialRequirements" : "Ability to lift 50 pounds", "qualificationsBasic" : "High School diploma or GED, 1 year of experience in a related field, Valid driver's license", "qualificationsPreferred" : "Bachelor's degree, Experience with behavior therapy, Registered Behavior Technician (RBT) certification", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Life Skills Autism Academy is looking for exceptional behavior technicians! Candidates must hold and maintain current certification as a Registered Behavior Technician (RBT) as issued by the Behavior Analyst Certification Board (BACB) or be willing to complete a 40 hour training course and sit for their RBT competency exam within 45 days of employment. Registered Behavior Technicians help the development of children who are on the Autism Spectrum by providing ABA (Applied Behavior Analysis) Therapy in a 1:1 setting under the supervision of a Board Certified Behavior Analyst. This therapy is used to increase critical developmental skills such as language and communication, social, and school readiness behaviors.. Pay Range: $18.00 - $24.00 per hour; negotiable based on experience, education, training, and skills. Schedule: Monday - Friday, 8:00am - 4:30pm Behavior Technician job responsibilities include: Provide direct client care in 1:1 and group settings utilizing a combination of intensive teaching and natural environment training. Follow the prescribed behavioral skill acquisition and behavior reduction protocols as outlined in client’s individualized treatment plan built by BCBA/BC. Collect, record, and summarize data on observable client behavior. Assist with parent and caregiver training in line with the client’s individualized treatment and behavior reduction protocols. Ensure documentation is completed on time and following established procedures. Effectively communicate with parents and caregivers regarding client progress as instructed by BCBA/BC. Utilize safe and appropriate procedures when working with clients and appropriately report all critical incidents and safety concerns. Maintain a clean, safe, and organized work and therapy environment. Assist BCBA/BC in preparation of client materials, behavior reduction assessments, and skills acquisition. Required Qualifications, Skills, and Knowledge: If extended an offer, must be willing to participate in the company’s background check process. Minimum of a High School Diploma of GED is required. Must have reliable transportation and in some cases, proof of driver’s license and valid car insurance. Need to be at least 18 years of age. Willing to obtain CPR and First Aid certification along with a TB test if you had not had one in the past year. Must be able to physically perform this job, including getting down on the floor and standing up many times, lifting up to 50lbs and the ability to run/move quickly if required to do so for the interaction with and safety and protection of the children with whom you work. Need to be very reliable and able to show up for each scheduled therapy appointment. Must always be professional in terms of both presentation and conduct. Need to have patience to help keep our clients on task. Able to maintain emotional control even if a client’s acting out physically or verbally. A positive attitude and drive to help a child acquire new skills is a must. Strong attention to detail with ability to do repetitive things in a precise manner. Ability to follow and carry out detailed instructions. Strong understanding of technology to be able to record data on a mobile device and navigate digital applications. Good written and verbal communication skills. Strong cultural competency with ability to remain flexible and open minded. Additional qualifications (not required): Experience working as a: Behavioral Technician, Working in some capacity with children with autism or other learning disabilities, Teacher’s Aid, Tutor, CNA, Caregiver or Home Health Aide Perks of Working at Centria: Structured career path in the field of Behavioral Analysis Discounts to hundreds of retail partners via our Benefit Hub Access to Centria’s Employee Assistance Plan with benefits around mental health and counseling Early wage access to employees through Rain - Work today, get paid tomorrow Unlimited opportunities to make an impact in the life of a special needs child We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, Veteran status, or disability status. This job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities, or working conditions associated with the position. Life Skills Autism Academy reserves the right to amend this job description at any time, with or without written notice. This pay scale range is the full range of potential wages Life Skills Autism Academy reasonably expects to pay for employees with this job title and this pay scale range varies dependent on job qualifications, performance, experience, and/or seniority. This range should not be interrupted to mean that Life Skills Autism Academy currently employs any employees with this job title at the bottom or top of the pay scale range. Life Skills Autism Academy reserves the right to amend this job description at any time, with or without written notice.", "summaryDescription" : "Center-Based Behavior Technician at Centria Autism. Skills: Behavioral Technician, ABA Therapy. Implement behavior intervention plans. 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Project team; PSI departments; Study vendors; Investigative sites; Monitors", "projectManagementSkills" : [ "Clinical research projects" ], "domainKnowledge" : "Clinical research; Contract Research Organization; Medicinal products; Therapeutic indications; Life Sciences", "domainList" : [ "clinical-research", "contract-research-organization", "medicinal-products", "therapeutic-indications", "life-sciences" ], "domainSpecificKnowledge" : [ "Clinical research", "Contract Research Organization", "Medicinal products", "Therapeutic indications", "Life Sciences" ], "toolProficiency" : [ "MS Office", "CTMS" ], "communicationSkills" : "Communication with sites; Communication with vendors; Communication with study vendors; Communication with project team; Communication with PSI departments; Communication with investigative sites", "documentationSkills" : "Document management; Maintain systems; Managing documents; Managing information; Trial Master File; Investigator Site Files; ISF checklists; Safety information flow", "continuousLearning" : "Onboarding program; Mentorship program; Professional growth", "problemSolvingSkills" : "Problem-solving abilities", "qualificationsBasic" : "College/University Degree (Life Sciences), Prior administrative experience in Clinical Research / CRO environment, Full working proficiency in Hebrew, Good English skills, Proficiency in standard MS Office applications", "qualificationsPreferred" : "Experience in an international setting", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. You will focus on facilitating research projects of novel medicinal products, while taking a step further in your professional career. Office-based role in Ra'anana, Israel The scope of responsibilities will include: Performs site management activities, documents and trackers management, and communication with the sites and study vendors. Site Management and Communication * Exchanges data, documents and other project relevant information between investigative sites, site vendors and the project team, and with other PSI departments * Ensures order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies * Ensures regulatory and ethics committee submissions and notifications * Ensures proper administration of sites and vendors payments, as applicable * Coordinates preparation for and follow-up on site, TMF and systems´ audits and inspections * Reviews and coordinates site-specific EDC completion and provides the site Monitor with regular updates on the completion status * Supports the organization of internal team meetings including preparation of agendas and minutes, and also of Investigator’s Meetings * Maintains study-specific and corporate tracking systems Document Management * Maintains Trial Master File and performs TMF oversight at country/site level * Prepares, distributes, and updates Investigator Site Files and ISF checklists * Revises and checks translation status Safety Management * Ensures proper safety information flow with investigative sites CTMS Management * Updates CTMS with project information * Supports Monitors in completion of all subject and site events information in CTMS, and meeting deadlines for site visits and visit reports ## Qualifications * College/University Degree (Life Sciences) * Prior administrative experience in Clinical Research / CRO environment, preferably in an international setting * Full working proficiency in Heberw and good English skills * Proficiency in standard MS Office applications (Word, Excel and PowerPoint) * Good organizational and planning skills, problem-solving abilities, flexibility * Detail-oriented, able to multi-task and work effectively in a fast-paced environment * Team-oriented with excellent customer service and interpersonal skills, including a positive attitude to tasks and projects *Please send your CV in English ## Additional Information As a privately owned mid-size CRO, we are constantly growing, offering plenty of opportunities for personal and professional growth. Our extensive onboarding and mentorship program will prepare you to fulfil your tasks with the highest standards, offering you: * Excellent and flexible working conditions * A unique combination of team collaboration and independent work * Competitive salary and benefits package * Opportunities for personal and professional growth Make the right call and take your career to a whole new level. Join a company that focuses on its people and invests in their professional development and success. [Do you want to make a difference? | | Discover PSI. - PSI CRO Recruitment Brochure](https://che01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fpsi-cro.turtl.co%2Fstory%2Fpsi-career-facts-and-figures%2Fpage%2F1&data=05%7C02%7COsnat.Nixon%40psi-cro.com%7C5f35eafe71164c306b5908de30a64017%7C6751a42d0cb04687a7821e3522d6718d%7C1%7C0%7C639001687751682103%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=PyJc5NKbw1dEYhQEz3EQHtLVs4161uj8eKt7HpQ49QM%3D&reserved=0)", "summaryDescription" : "Site Management Associate (SMA) - Including CTA responsibilities and more! at PSI CRO. Skills: Site management, Document management, Clinical research. Perform site management activities. 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and project information, Ensure order, receipt, inventory storage, distribution, return/recall and, Ensure regulatory and ethics committee submissions and notifications, Ensure proper administration of sites and vendors payments, Coordinate preparation for and follow-up on site, TMF, Review and coordinate site-specific EDC completion, Provide Monitor with regular updates on completion status, Support organization of internal team meetings, Prepare agendas and minutes for meetings, Support organization of Investigator’s Meetings, Maintain study-specific and corporate tracking systems, Maintain Trial Master File, Perform TMF oversight at country/site level, Prepare, distribute, and update Investigator Site Files, Prepare, distribute, and update ISF checklists, Revise and check translation status, Ensure proper safety information flow with investigative sites, Update CTMS with project information, Support Monitors in completion of subject and site, Support Monitors in meeting deadlines for site visits", "teamCollaboration" : "International team; Project team; PSI departments; Study vendors; Monitors", "domainKnowledge" : "Clinical research; Contract Research Organization; Medicinal products", "domainList" : [ "clinical-research", "contract-research-organization", "medicinal-products" ], "domainSpecificKnowledge" : [ "Clinical research", "Contract Research Organization", "Medicinal products" ], "toolProficiency" : [ "MS Office", "Word", "Excel", "PowerPoint" ], "communicationSkills" : "Communication with sites; Communication with vendors; Communication with study vendors; Communication with project team; Communication with PSI departments; Safety information flow", "documentationSkills" : "Document management; Tracker management; Trial Master File; Investigator Site Files; ISF checklists; Translation status", "continuousLearning" : "Onboarding program; Mentorship program; Professional growth", "problemSolvingSkills" : "Problem-solving abilities", "qualificationsBasic" : "College/University Degree (Life Sciences), Prior administrative experience in Clinical Research / CRO environment, Full working proficiency in Hebrew, Good English skills, Proficiency in standard MS Office applications", "qualificationsPreferred" : "Experience in an international setting", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. You will focus on facilitating research projects of novel medicinal products, while taking a step further in your professional career. Office-based role in Ra'anana, Israel The scope of responsibilities will include: Performs site management activities, documents and trackers management, and communication with the sites and study vendors. Site Management and Communication * Exchanges data, documents and other project relevant information between investigative sites, site vendors and the project team, and with other PSI departments * Ensures order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies * Ensures regulatory and ethics committee submissions and notifications * Ensures proper administration of sites and vendors payments, as applicable * Coordinates preparation for and follow-up on site, TMF and systems´ audits and inspections * Reviews and coordinates site-specific EDC completion and provides the site Monitor with regular updates on the completion status * Supports the organization of internal team meetings including preparation of agendas and minutes, and also of Investigator’s Meetings * Maintains study-specific and corporate tracking systems Document Management * Maintains Trial Master File and performs TMF oversight at country/site level * Prepares, distributes, and updates Investigator Site Files and ISF checklists * Revises and checks translation status Safety Management * Ensures proper safety information flow with investigative sites CTMS Management * Updates CTMS with project information * Supports Monitors in completion of all subject and site events information in CTMS, and meeting deadlines for site visits and visit reports ## Qualifications * College/University Degree (Life Sciences) * Prior administrative experience in Clinical Research / CRO environment, preferably in an international setting * Full working proficiency in Heberw and good English skills * Proficiency in standard MS Office applications (Word, Excel and PowerPoint) * Good organizational and planning skills, problem-solving abilities, flexibility * Detail-oriented, able to multi-task and work effectively in a fast-paced environment * Team-oriented with excellent customer service and interpersonal skills, including a positive attitude to tasks and projects *Please send your CV in English ## Additional Information As a privately owned mid-size CRO, we are constantly growing, offering plenty of opportunities for personal and professional growth. Our extensive onboarding and mentorship program will prepare you to fulfil your tasks with the highest standards, offering you: * Excellent and flexible working conditions * A unique combination of team collaboration and independent work * Competitive salary and benefits package * Opportunities for personal and professional growth Make the right call and take your career to a whole new level. Join a company that focuses on its people and invests in their professional development and success. [Do you want to make a difference? | | Discover PSI. - PSI CRO Recruitment Brochure](https://che01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fpsi-cro.turtl.co%2Fstory%2Fpsi-career-facts-and-figures%2Fpage%2F1&data=05%7C02%7COsnat.Nixon%40psi-cro.com%7C5f35eafe71164c306b5908de30a64017%7C6751a42d0cb04687a7821e3522d6718d%7C1%7C0%7C639001687751682103%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=PyJc5NKbw1dEYhQEz3EQHtLVs4161uj8eKt7HpQ49QM%3D&reserved=0)", "summaryDescription" : "Site Management Associate (SMA) - Including CTA responsibilities and more! at PSI CRO. Skills: Site management, Document management, CTMS management. Perform site management activities. Manage documents and trackers", "postedDate" : "2026-06-11T11:46:08.000", "createdAt" : "2026-06-14T18:29:04.490", "lastUpdated" : "2026-06-16T04:36:21.635", "ingestTimestamp" : "2026-06-14T18:29:04.490", "mongoId" : "6a2d3f1074d8ee00a0b34806", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "100k-150k", "hasSalary" : false, "allSkills" : [ "Site management", "Document management", "Vendor management", "Clinical supplies management", "Regulatory submissions", "Ethics committee submissions", "Site audits", "TMF oversight", "Safety information flow", "CTMS management", "Clinical research", "Contract Research Organization", "Medicinal products", "MS Office", "Word", "Excel", "PowerPoint" ], "skillCount" : 17, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Junior", "dataQualityScore" : 1.0, "daysOld" : 4, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c903b74d8ee00a097faff", "title" : "Center-Based Behavior Technician", "company" : "Centria Autism", "industry" : "Healthcare", "salary" : { "min" : 20.0, "max" : 23.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Lawrence, Indiana, United States", "locations" : [ "Lawrence", "Indiana", "United States" ], "certifications" : [ "RBT certification" ], "timestamp" : "2026-06-16T05:23:27.113", "fingerprint" : "d57ca33949867bf2c3eaa2026364882364df93588fbd3f9adfa0a27d8d85112d", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/centriaautism/jobs/8588932002", "externalId" : "8588932002", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Lawrence", "state" : "Indiana", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.8400395,-86.4880717" } ], "locationText" : "Lawrence, Indiana, United States", "minimumEducation" : "High school diploma or GED", "experienceMinYears" : 0, "experienceMaxYears" : 2, "experienceLevel" : "Entry", "professionalSkills" : [ "Behavioral therapy", "Data collection" ], "hardSkillsList" : [ "Applied Behavior Analysis" ], "hardSkills" : [ { "name" : "Applied Behavior Analysis", "level" : "intermediate" } ], "majorSkills" : "Behavior Technician, ABA Therapy", "majorSkillsList" : [ "Behavior Technician", "ABA Therapy" ], "coreResponsibilities" : "Implement behavior intervention plans, Collect data on client progress, Provide direct therapy, Assist with client daily living skills, Maintain client records, Collaborate with the treatment team", "teamCollaboration" : "Treatment team", "domainKnowledge" : "Autism Spectrum Disorder; Applied Behavior Analysis", "domainList" : [ "autism-spectrum-disorder", "applied-behavior-analysis" ], "domainSpecificKnowledge" : [ "Autism Spectrum Disorder", "Applied Behavior Analysis" ], "documentationSkills" : "Client records", "qualificationsBasic" : "High school diploma or GED, 0+ years experience", "qualificationsPreferred" : "Experience with ABA principles, Experience working with children, Experience with autism spectrum disorder", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "We are looking for enthusiastic individuals to join our team as Behavior Technicians. As a Behavior Technician, you will have the opportunity to make a real difference in the lives of children with autism. In this role, you will work one-on-one with children, implementing individualized behavior intervention plans under the guidance of a Board Certified Behavior Analyst (BCBA). You will use evidence-based techniques to teach communication, social, and daily living skills while reducing interfering behaviors. We are looking for candidates who are passionate about helping children with autism reach their full potential. You will need to be patient, compassionate, and able to work well in a team environment. We will provide comprehensive training so that you are equipped and empowered to help each child, even if you don’t currently have experience. Children can be unpredictable and potentially confrontational, so this role is not for the weak of spirit, mind, or body. Part of the joy of working with kids is exercise! Our clients move, so you need to be comfortable standing, walking, sitting, grasping, reaching, bending, kneeling, crouching, squatting, lifting, and at times carrying children or objects that weigh up to 50 pounds At the end of each day, you will go home knowing that you have made a meaningful impact on the life of a child and their family. Join us and become a part of a dedicated team that is changing lives for the better. Apply now to start your journey as a Behavior Technician with us! Pay Range: $20 - $23 Requirements: Passionate about helping children with autism. Patient, compassionate, and able to work well in a team. 18+ years of age High school diploma or GED Ability to obtain a CPR, First Aid Certification and Tuberculosis test (if you haven’t had one in the last year) Ability to pass a pre employment background check Ability to move in various positions (sit, squat, bend, etc.) Ability to lift and carry up to 50 pounds. Perks of Working at Centria: Structured career path in the field of Behavioral Analysis Discounts to hundreds of retail partners via our Benefit Hub Access to Centria’s Employee Assistance Plan with benefits around mental health and counseling Early wage access to employees through Rain - Work today, get paid tomorrow! Unlimited opportunities to make an impact in the life of a special needs child We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, Veteran status, or disability status. This job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities, or working conditions associated with the position. This pay scale range is the full range of potential wages Centria Autism reasonably expects to pay for employees with this job title and this pay scale range varies dependent on job qualifications, performance, experience, and/or seniority. This range should not be interrupted to mean that Centria Autism currently employs any employees with this job title at the bottom or top of the pay scale range. Centria reserves the right to amend this job description at any time, with or without written notice.", "summaryDescription" : "Center-Based Behavior Technician at Centria Autism. Skills: Behavior Technician, ABA Therapy. Implement behavior intervention plans. Collect data on client progress", "postedDate" : "2026-06-14T20:07:31.961", "createdAt" : "2026-06-14T20:07:31.961", "lastUpdated" : "2026-06-16T05:23:27.113", "ingestTimestamp" : "2026-06-14T20:07:31.961", "mongoId" : "6a2c903b74d8ee00a097faff", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 41600, "salaryAnnualMax" : 47840, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Applied Behavior Analysis", "Behavior Technician", "ABA Therapy", "Behavioral therapy", "Data collection", "Autism Spectrum Disorder", "RBT certification" ], "skillCount" : 7, "jobCategory" : "healthcare", "jobSubcategory" : "support", "seniorityLevel" : "Entry", "dataQualityScore" : 0.8888889, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2c903c74d8ee00a097fb19", "title" : "Center-Based Behavior Technician", "company" : "Centria Autism", "industry" : "Healthcare", "salary" : { "min" : 41600.0, "max" : 47840.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Indianapolis, Indiana, United States", "locations" : [ "Indianapolis", "Indiana", "United States" ], "certifications" : [ "Registered Behavior Technician (RBT)" ], "timestamp" : "2026-06-16T04:34:37.747", "fingerprint" : "ea327d59ff8eb64919422de3a667b23338212406bd2fa9c2697056f94c401b08", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/centriaautism/jobs/8589697002", "externalId" : "8589697002", "industryFunction" : { }, "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", "minimumEducation" : "High School", "professionalSkills" : [ "Behavioral therapy", "Data collection", "Clinical documentation" ], "hardSkillsList" : [ "Applied Behavior Analysis", "Data analysis", "Behavioral intervention" ], "hardSkills" : [ { "name" : "Applied Behavior Analysis", "level" : "intermediate" }, { "name" : "Data analysis", "level" : "intermediate" }, { "name" : "Behavioral intervention", "level" : "intermediate" } ], "majorSkills" : "Behavioral Technician, Autism Spectrum Disorder, Clinical Care", "majorSkillsList" : [ "Behavioral Technician", "Autism Spectrum Disorder", "Clinical Care" ], "coreResponsibilities" : "Implement treatment plans, Collect data, Provide direct patient care, Maintain patient records, Collaborate with clinical team, Communicate with families, Adhere to safety protocols, Attend training sessions", "teamCollaboration" : "Clinical team; Families", "domainKnowledge" : "Autism Spectrum Disorder; Behavioral science; HIPAA regulations", "domainList" : [ "autism-spectrum-disorder", "behavioral-science", "hipaa-regulations" ], "domainSpecificKnowledge" : [ "Autism Spectrum Disorder", "Behavioral science", "HIPAA regulations" ], "toolProficiency" : [ "EHR systems", "Data tracking tools" ], "communicationSkills" : "Patient communication; Family communication", "documentationSkills" : "Clinical documentation; Data collection", "continuousLearning" : "Training sessions", "problemSolvingSkills" : "Behavioral intervention", "specialRequirements" : "Ability to lift 50 pounds", "outcomesObjectives" : "Improve patient outcomes; Ensure patient safety", "qualificationsBasic" : "High School diploma or GED, Valid driver's license, Reliable transportation, Ability to lift 50 pounds", "qualificationsPreferred" : "Bachelor's degree, Experience working with children, Experience in a clinical setting", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Our Story Life Skills Autism Academy, a division of Centria Autism, is a high-commitment, center-based ABA Therapy program. Rooted in the evidence that early, high-intensive ABA Therapy leads to the greatest potential reached by children on the autism spectrum, we specialize in providing services to young children. As leading experts in the field of Applied Behavior Analysis (ABA), the academy's highly-trained clinicians develop individualized, one-on-one programs that help children break down routine tasks into manageable steps. This type of therapy helps children with autism improve communication ability, daily living skills, and the social behaviors necessary to thrive in school, at home, and in their community. Schedule: Full time, Monday-Friday 8:30 am-4:30 pm, in center Compensation & Benefits: Pay Range: $20-$23, increases based on education and experience Paid time off Benefits plan - medical, dental, vision, etc. Uncapped Structured Pay Plan Tuition Discount Program Early wage access to employees through Rain - Work today, get paid tomorrow! Practicum Program - earn your supervision hours! Registered Behavior Technician job responsibilities include: Provide direct client care in 1:1 and group settings utilizing a combination of intensive teaching and natural environment training Follow the prescribed behavioral skill acquisition and behavior reduction protocols as outlined in the client's individualized treatment plan built by BCBA/BC Collect, record, and summarize data on observable client behavior Assist with parent and caregiver training in line with the client’s individualized treatment and behavior reduction protocols Ensure documentation is completed on time and following established procedures Effectively communicate with parents and caregivers regarding client progress as instructed by BCBA/BC Utilize safe and appropriate procedures when working with clients and appropriately report all critical incidents and safety concerns Maintain a clean, safe, and organized work and therapy environment Assist BCBA/BC in the preparation of client materials, behavior reduction assessments, and skills acquisition Required Qualifications, Skills, and Knowledge: Must hold and maintain current certification as a Registered Behavior Technician (RBT) as issued by the Behavior Analyst Certification Board (BACB) Must be willing to participate in the company’s background check process A minimum of a High School Diploma or GED is required Must have reliable transportation Must be at least 18 years of age Willing to obtain CPR and First Aid certification Willing to obtain a tuberculosis (TB) test annually Must be able to physically perform this job, including getting down on the floor and standing up many times, lifting up to 50lbs, and the ability to run/move quickly if required to do so for the interaction with and safety and protection of the children with whom you work Strong attention to detail with the ability to do repetitive things in a precise manner Ability to follow and carry out detailed instructions Strong understanding of technology to be able to record data on a mobile device and navigate digital applications Good written and verbal communication skills Strong cultural competency with the ability to remain flexible and open-minded We are an equal-opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, Veteran status, or disability status. This job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities, or working conditions associated with the position. Centria reserves the right to amend this job description at any time, with or without written notice.", "summaryDescription" : "Center-Based Behavior Technician at Centria Autism. Skills: Behavioral Technician, Autism Spectrum Disorder, Clinical Care. Implement treatment plans. 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As a Behavior Technician, you will have the opportunity to make a real difference in the lives of children with autism. In this role, you will work one-on-one with children, implementing individualized behavior intervention plans under the guidance of a Board Certified Behavior Analyst (BCBA). You will use evidence-based techniques to teach communication, social, and daily living skills while reducing interfering behaviors. We are looking for candidates who are passionate about helping children with autism reach their full potential. You will need to be patient, compassionate, and able to work well in a team environment. We will provide comprehensive training so that you are equipped and empowered to help each child, even if you don’t currently have experience. Children can be unpredictable and potentially confrontational, so this role is not for the weak of spirit, mind, or body. Part of the joy of working with kids is exercise! Our clients move, so you need to be comfortable standing, walking, sitting, grasping, reaching, bending, kneeling, crouching, squatting, lifting, and at times carrying children or objects that weigh up to 50 pounds. At the end of each day, you will go home knowing that you have made a meaningful impact on the life of a child and their family. Join us and become a part of a dedicated team that is changing lives for the better. Apply now to start your journey as a Behavior Technician with us! Pay Range: $17 - $20 Requirements: Passionate about helping children with autism Patient, compassionate, and able to work well in a team 18+ years of age High school diploma or GED Ability to obtain a CPR, First Aid Certification and Tuberculosis test (if you haven’t had one in the last year) Ability to pass a pre employment background check Ability to move in various positions (sit, squat, bend, etc.) Ability to lift and carry up to 50 pounds Additional qualifications (not required): Experience working as a: Behavioral Technician, Working in some capacity with children with autism or other learning disabilities, Teacher’s Aid, Tutor, CNA, Caregiver or Home Health Aide Perks of Working at Centria: Structured career path in the field of Behavioral Analysis Discounts to hundreds of retail partners via our Benefit Hub Access to Centria’s Employee Assistance Plan with benefits around mental health and counseling Early wage access to employees through Rain - Work today, get paid tomorrow! Unlimited opportunities to make an impact in the life of a special needs child We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, Veteran status, or disability status. This job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities, or working conditions associated with the position. This pay scale range is the full range of potential wages Centria Autism reasonably expects to pay for employees with this job title and this pay scale range varies dependent on job qualifications, performance, experience, and/or seniority. This range should not be interrupted to mean that Centria Autism currently employs any employees with this job title at the bottom or top of the pay scale range. Centria reserves the right to amend this job description at any time, with or without written notice.", "summaryDescription" : "Center-Based Behavior Technician at Centria Autism. Skills: Behavior Technician, ABA Therapy. Implement behavior intervention plans. 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TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

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Plans and implements nursing care; documents nursing assessments; identifies and reports situations requiring further intervention; formulates and communicates goal-directed plan of care; assures patient rights. Responsible for performing job duties in accordance with the mission, vision and values of Tampa General Hospital and principles of quality improvement. Graduate of an accredited School of Nursing. Licensure to practice as a Registered Nurse in the State of Florida. Tampa", "summaryDescription" : "Clinical Nurse-Surgical/Trauma ICU Step Down Unit at Tampa General Hospital. Skills: Surgical nursing, Trauma nursing, ICU care. Deliver nursing care to patients. 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This is a dynamic role within Adult Social Care, requiring a confident practitioner with a strong understanding of statutory duties, safeguarding processes, and care planning. The successful candidate will play a key role in delivering high-quality, person-centred services, supporting adults with varying levels of need while promoting independence, safety, and wellbeing within the community. What will your responsibilities be? Undertaking Care Act 2014 needs assessments and reviews in line with statutory requirements. Completing and managing Safeguarding Enquiries (Section 42), ensuring timely and proportionate responses to risk. Developing and implementing person-centred care and support plans. Supporting individuals through community-based interventions, promoting independence and preventing escalation of need. Carrying out Community DoLS work in line with legislation and best practice. Managing a varied caseload, including complex and high-risk cases. Working collaboratively with multi-disciplinary teams, including health professionals and partner agencies. Maintaining accurate, timely, and high-quality case records in line with organisational standards. Applying strong professional judgement within legal and policy frameworks. Qualifications & Experience: To be successful in this role you must have, • Professional Qualification: MA, BA, BSc in Social Work, Diploma in Social Work, or CQSW. • Registration: Must be registered with Social Work England. • Experience: Strong experience within Adult Social Care. Demonstrable experience completing Safeguarding Enquiries. Experience undertaking Care Act assessments, care planning, and reviews. Practical experience working with Community DoLS. Ability to manage a complex caseload effectively. • Knowledge: Sound knowledge of all aspects of Adult Social Work practice. Strong understanding of relevant legislation, including the Care Act 2014 and safeguarding responsibilities. • Skills: Excellent assessment and analytical skills. Strong written and verbal communication abilities. Ability to work independently and within a team environment. Good organisational and time management skills. Why Liquid Personnel? Free DBS and compliance service Twice weekly payroll and ‘Faster Pay’ service, getting you paid more quickly Access to exclusive roles that aren’t available from other agencies Free access to Liquid’s exclusive social work training and CPD portal Your own dedicated consultant with extensive social work knowledge Access to a wide selection of social work positions across the UK “Refer a Friend” bonus – get £500 for each social worker you refer who we successfully place* “Find your own job” bonus – get £250 for bringing your own position to us * Liquid Personnel is an equal opportunities employer. Liquid Personnel Ltd is acting as an Employment Business in relation to this vacancy. * Terms and conditions apply to our bonus schemes. Reasonable Adjustments: If you consider yourself to have a disability or require any reasonable adjustment during the recruitment process or within the workplace, please highlight this at the earliest opportunity by contacting our team. With this information, we will provide appropriate support to you throughout the process and into your work placement. We are unable to support or accept applications from candidates who are residents within the Red or Amber list of the Code of practice for the international recruitment of health and social care personnel in England, based on the World Health Organisation (WHO) Workforce Support and Safeguard List. BH - 199722 GH - 35179", "summaryDescription" : "Social Worker - Adult, Care and Support Team at Liquid Personnel. Skills: Adult Social Care, Safeguarding, Care Act 2014. 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As a Behavior Technician, you will have the opportunity to make a real difference in the lives of children with autism. In this role, you will work one-on-one with children, implementing individualized behavior intervention plans under the guidance of a Board Certified Behavior Analyst (BCBA). You will use evidence-based techniques to teach communication, social, and daily living skills while reducing interfering behaviors. We are looking for candidates who are passionate about helping children with autism reach their full potential. You will need to be patient, compassionate, and able to work well in a team environment. We will provide comprehensive training so that you are equipped and empowered to help each child, even if you don’t currently have experience. Children can be unpredictable and potentially confrontational, so this role is not for the weak of spirit, mind, or body. Part of the joy of working with kids is exercise! Our clients move, so you need to be comfortable standing, walking, sitting, grasping, reaching, bending, kneeling, crouching, squatting, lifting, and at times carrying children or objects that weigh up to 50 pounds. At the end of each day, you will go home knowing that you have made a meaningful impact on the life of a child and their family. Join us and become a part of a dedicated team that is changing lives for the better. Apply now to start your journey as a Behavior Technician with us! Pay Range: $17 - $20 Requirements: Passionate about helping children with autism Patient, compassionate, and able to work well in a team 18+ years of age High school diploma or GED Ability to obtain a CPR, First Aid Certification and Tuberculosis test (if you haven’t had one in the last year) Ability to pass a pre employment background check Ability to move in various positions (sit, squat, bend, etc.) Ability to lift and carry up to 50 pounds Perks of Working at Centria: Structured career path in the field of Behavioral Analysis Discounts to hundreds of retail partners via our Benefit Hub Access to Centria’s Employee Assistance Plan with benefits around mental health and counseling Early wage access to employees through Rain - Work today, get paid tomorrow! Candidates must obtain an Registered Behavior Technician Certification after completing onboarding Unlimited opportunities to make an impact in the life of a special needs child We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, Veteran status, or disability status. This job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities, or working conditions associated with the position. This pay scale range is the full range of potential wages Centria Autism reasonably expects to pay for employees with this job title and this pay scale range varies dependent on job qualifications, performance, experience, and/or seniority. This range should not be interrupted to mean that Centria Autism currently employs any employees with this job title at the bottom or top of the pay scale range. Centria reserves the right to amend this job description at any time, with or without written notice.", "summaryDescription" : "Center-Based Behavior Technician at Centria Autism. Skills: Behavioral Technician, Clinical support. Implement behavior intervention plans. Collect and record client data", "postedDate" : "2026-06-14T20:11:31.939", "createdAt" : "2026-06-14T20:11:31.939", "lastUpdated" : "2026-06-16T05:08:08.523", "ingestTimestamp" : "2026-06-14T20:11:31.939", "mongoId" : "6a2c903d74d8ee00a097fb5a", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 35360, "salaryAnnualMax" : 41600, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Behavioral intervention", "Data analysis", "Behavioral Technician", "Clinical support", "Behavioral therapy", "Data collection", "Client interaction", "Autism Spectrum Disorder", "Applied Behavior Analysis", "Registered Behavior Technician (RBT)", "Microsoft Office Suite" ], "skillCount" : 11, "jobCategory" : "healthcare", "jobSubcategory" : "support", "seniorityLevel" : "Entry", "dataQualityScore" : 0.7777778, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 } ], "status" : 200, "message" : "support protein based assays including protein extraction pull down assays and gel electrophoresis jobs", "metadata" : { "title" : "support protein based assays including protein extraction pull down assays and gel electrophoresis" }, "pagination" : { "page" : 0, "limit" : 50, "totalCount" : 33254, "totalPages" : 666, "hasNext" : true, "hasPrevious" : false } }

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