QC Laboratory Supervisor (2nd shift)
On-siteGrand Rapids, Michigan, United States
Job Summary
Manage day-to-day prioritization of routine, in-process, stability, and finished product work while overseeing all laboratory chemical and equipment use. Supervise lab personnel, including staff performance and creation of staff schedules to ensure over-time/weekend coverage for manufacturing support. Lead training of new employees, maintain documentation, and independently author or edit internal test methods and standard operating procedures. Support the OOS system, Laboratory Investigations, and assist in related CAPAs and non-conformances. Comply with laboratory safety guidelines and inform management of any concerns. Deliver staff performance evaluations, develop individual goals, and address progress via routine 1x1 meetings. Establish and maintain good technique regarding aseptic environments. Work with management to maintain the working schedule of all work flowing through the QC Analytical Lab.
Required Qualifications
- Bachelor's degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology)
- 5 years pharmaceutical or testing experience
- Proficient computer skills in Microsoft Word, Excel, and Outlook
- Weekend support necessary depending on the production schedule
Desired Qualifications
- Knowledge of physical, chemical, and instrumental analysis of raw material, active pharmaceutical ingredients, excipients and finished pharmaceutical products
- Experience with various types of laboratory instruments including: HPLC, UHPLC, UPLC, GC, UV-Vis, FTIR, etc.
- Candidate should understand and have experience with pharmaceutical manufacturing and analytical laboratories in regulated environments under FDA, ICH, and EMA guidelines
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