Role OverviewThe QA Supervisor provides direction and leadership to the Grand River Aseptic Manufacturing (GRAM) Quality Systems with oversight Finishing Operations (Inspection, Labeling, Packaging). This position works closely with all levels of the Operations, Technical Services, Validation, QC (Microbiology and Analytical Chemistry), Business and Finance teams.
What You Will Do
Provide supervision to Quality Specialists and Quality Technicians of various levels, ensure Quality support and oversight of Finishing operations across all shifts, and perform Quality Assurance review and approval of cGMP documentation.
Why It Might Be a Fit
The ideal candidate will have a thorough understanding of cGMP, FDA guidelines and multinational regulatory standards, and will be able to motivate and coach Quality Specialists and Quality Technicians.
Requirements
- Bachelor’s degree in Life Sciences or a related field
- 4+ years related work experience
- At least 3 years prior experience in a QA Specialist role
- A thorough understanding of cGMP, FDA guidelines and multinational regulatory standards
- Proficient computer skills in Microsoft Word, Excel, and Outlook
Benefits
- Medical, prescription, dental, vision, life insurance, and disability benefits
- 401(k) program with 100% vesting
- Generous off-shift premiums
- 16 hours of paid volunteer time per calendar year
- Up to 13 days of PTO per calendar year
- 1 hour of time off for every 30 hours worked
- 10 paid holidays per calendar year
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