2nd Shift QA Auditor – cGMP Pharma Manufacturing
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Quality Assurance - QA/QC
Production QC/QA, Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers -
Manufacturing / Production
Production QC/QA, Regulatory Compliance Specialist
Job Description & How to Apply Below
Tower Laboratories, Ltd. in Clinton, Connecticut is seeking a Quality Auditor for the 2nd shift to ensure our effervescent products meet all specifications and regulatory requirements.
The role emphasizes quality system enforcement, collaboration with production, and thorough documentation across the production life cycle. The position supports a family-owned company with a comprehensive benefits package including a 401(k) match, medical/dental/vision coverage, and paid holidays.
We have an opening for a 2nd Shift QA Auditor – cGMP Pharma Manufacturing in Clinton, CT, United States within Finance, Engineering.
We appreciate your interest in this position.
Join Tower Laboratories, Ltd. and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the 2nd Shift QA Auditor – cGMP Pharma Manufacturing role at Tower Laboratories, Ltd., based in Clinton, CT, United States.
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