Quality Control Analyst – 1st Shift
Job in
Franklin, Connecticut, USA
Listed on 2026-01-12
Listing for:
Stryker Group
Full Time
position Listed on 2026-01-12
Job specializations:
-
Healthcare
Data Scientist, Medical Technologist & Lab Technician, Medical Science
Job Description & How to Apply Below
Location: Franklin
1st Shift: Mon - Fri 8:00 AM to 5:00 PM, OT as needed
What you will do:
The QC Analyst I will perform routine and complex analytical testing to support lot release, stability, and method development, while accurately documenting results and ensuring all work meets cGMP/cGLP standards.
- Perform routine procedures and complex analytical methods for lot release and stability testing of raw materials, reagents, and products, and prepare technical reports and documentation
- Test and record measurements of various product attributes, including pH, concentration, identity, purity, impurities, and bio-potency.
- Perform studies to qualify analytical standards, assay controls, and critical reagents.
- Complete documentation to show that tests have been performed according to approved methods and that all results are recorded accurately.
- Maintain laboratory operations in conformance with cGMP/cGLP standards.
- Monitor and record equipment parameters (temperature charts, gas levels, and liquid nitrogen levels).
- Monitor and maintain adequate quantities of laboratory supplies.
- Assist the Quality Control team with technical evaluations of non-conforming test results and events to determine root cause; recommend corrective actions.
- Participate in studies to develop and validate new analytical methods.
What you need:
Required Qualifications- Bachelor’s degree in biology, biochemistry, microbiology or chemistry
- Experience with various analytical equipment and methods·
- Experience with the application of statistics for data analysis
- Experience with computer software (WORD, Excel, etc.)
- Master’s degree in biology, biochemistry, microbiology, or chemistry
- 1 - 2 years of recent and applicable industry experience, preferably in a pharmaceutical quality control laboratory
- Advanced technical knowledge of analytical methods and function and maintenance of related instruments (including, but not limited to HPLC, UHPLC, UV/Vis spectrophotometers, SDS-PAGE, capillary electrophoresis, brightfield and fluorescence microscopy, cell counters, protein analysis)
- Experience with aseptic technique and mammalian cell cultures
- Experience with inspections, audits, and regulatory agencies/governing bodies.
- Knowledge of GLP/GMP, 21 CFR 211, 21 CFR 820, and ISO
13485 standards and regulations - Experience maintaining qualified laboratory equipment and creating/reviewing technical documents for an FDA-regulated laboratory
*** Highly qualified candidates with alternate, but applicable experience will be considered, including related academic and commercial laboratory research.***
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