About The Position
The Quality Control Senior Associate Scientist performs cGMP analytical laboratory analysis for MilliporeSigma’s Quality Control department, supporting activities at the Madison and Verona sites. Work may include analysis and review of incoming raw materials, in-process materials, and final products, as well as method validation or qualification, cleaning, and environmental monitoring. Analytical techniques may include HPLC, GC, KF, DSC, TGA, IR, MS, NMR, and XRPD. The role may also involve initiating and reviewing deviations, OOS/OOT events, change controls, and CAPAs. The position supports process-improvement initiatives, teamwork, a clean and safe work area, and an audit-ready laboratory. The successful candidate is willing to contribute to the company’s overall success beyond specific job duties. The schedule is Friday through Sunday, 6:30 a.m. to 7:00 p.m. The role does not offer work-authorization sponsorship; external applicants must be eligible to work in the United States.
Requirements
- Bachelor’s degree in Chemistry, Biology, or another Life Science discipline.
- At least 3 years of experience in a GLP or cGMP environment.
- Must be eligible to work in the United States; work-authorization sponsorship is not offered.
- Willingness to contribute beyond specific job duties.
Nice To Haves
- At least 4 years of experience in a GMP analytical manufacturing or testing laboratory.
- Understanding of 21 CFR Parts 11, 210, and 211, and ICH Q7.
- Experience with chemical analyses including HPLC, GC, KF, DSC, TGA, IR, MS, NMR, and/or XRPD.
- Excellent written and verbal communication skills.
- Good documentation practices and attention to detail.
- Knowledge and understanding of analytical chemistry techniques.
Responsibilities
- Perform and review cGMP laboratory analysis, including incoming raw material, in-process, and final product testing.
- Perform method validation or qualification, cleaning, and environmental monitoring activities.
- Use analytical techniques and instruments such as HPLC, GC, KF, DSC, TGA, IR, MS, NMR, and XRPD, among other tests and instruments.
- Initiate and review deviations, OOS/OOT events, change controls, and CAPAs as needed.
- Participate in process-improvement initiatives and work collaboratively in a team environment.
- Maintain a clean and safe work area and help keep the laboratory audit-ready.
- Contribute to the overall success of the company by assisting beyond specific job duties.
Benefits
- Health insurance
- Paid time off (PTO)
- Retirement contributions
- Other perquisites
- Position may be eligible for sales or performance-based bonuses.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
