Siegfried
Pharmaceutical
QualityControlAnalyst
Neural analysis suggests this role is
optimal for Entry candidates.
“Quality Control Analyst at Siegfried. Skills: Analytical chemistry, Chromatography, Quality Control. Perform analytical chemistry assays. Perform chromatography”
Industry & Context.
Define problems; Collect data; Establish facts; Draw valid conclusions; Interpret technical instructions; Deal with abstract variables
Saturday - Tuesday (nights 4x10 hour shifts), Work under pressure, Limited supervision, Physical demands, Exposure to fumes or airborne particles, Exposure to toxic or caustic chemicals, Exposure to wet and/or humid conditions, Exposure to moving mechanical parts, Exposure to high, precarious places, Exposure to outside weather, Risk of electrical shock, Moderate noise level, Generate hazardous waste, Familiar with RCRA training requirements, Understand waste labeling, Understand secondary containment, Understand chemical compatibility, Understand storage time limits, Understand container size and quantity limits, Understand container integrity, Understand improper disposal of hazardous materials
What They're Looking For.
Must Have
Bachelor’s degree in chemistry or related field, 0-3 years’ pharmaceutical experience or equivalent combination of education and experience, Perform analytical testing for incoming, in-process and final products, and stability samples, Perform chromatography (Liquid/GC), Perform wet chemistry assays, Regularly perform water sample collection, Back up for QC analytical instrument maintenance and calibration, Performance of QC general laboratory equipment maintenance, laboratory housekeeping, preparation of the laboratory for audits, Assist in the review of QC data, provide summaries to management, Assist QC Management, as needed, in the completion of OOS, deviations and CAPAs investigations, Backup for QC analytical sample receipt, login, processing, shipment, tracking, distribution of test results, and closure, Ability to apply advanced mathematical concepts, Ability to apply mathematical operations, Ability to define problems, collect data, establish facts, and draw valid conclusions, Ability to interpret an extensive variety of technical instructions, deal with several abstract and concrete variables, Proficient use of computer software, Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600)
Nice to Have
Experience in a cGMP or GLP pharmaceutical industry environment, ISO 9001 and 13485
What You'll Do.
Perform analytical chemistry assays
Perform chromatography
Perform wet chemistry assays
Perform water sample collection
Back up instrument maintenance
Perform laboratory equipment maintenance
Maintain laboratory housekeeping
Prepare laboratory for audits
Provide data summaries
Assist with OOS investigations
Assist with deviation investigations
Assist with CAPA investigations
Backup sample receipt
Distribute test results
How You'll Work.
Team & Collaboration
Work with management; Collaborate with product team
Communication Scope
Excellent verbal and written communication; Respond to questions from groups; Present information
Process & Methodology
Manage multiple projects independently
Full Job Description
"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions—offering long-term opportunities to grow and make an impact. **Your Role:** The Quality Control Analyst I is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished APIs, and stability samples. **Your Profile:** * _**Schedule: Saturday - Tuesday (nights 4x10 hour shifts)**_ Perform analytical testing for incoming, in-process and final products, and stability samples using equipment such as balances, pipettes, pH meter, UV/Visible spectrophotometer, Total Organic Carbon analyzer, etc. Perform chromatography (Liquid/GC) after extensive qualification and training Perform wet chemistry assays Regularly perform water sample collection Back up for QC analytical instrument maintenance and calibration Performance of QC general laboratory equipment maintenance, laboratory housekeeping and preparation of the laboratory for audits Assist in the review of QC data and provide summaries to management as needed Assist QC Management, as needed, in the completion of OOS, deviations and CAPAs investigations for QC Backup for QC analytical sample receipt for internal testing, outside laboratory testing, login, processing, shipment, tracking, distribution of test results, and closure. **Your Benefits:** Education, experience, certification and licensures Required · Bachelor’s degree in chemistry or related field · Minimum 0-3 years’ pharmaceutical experience or e
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