Job Description
Essential Functions:
- Supervise QC laboratory operations and testing activities
- Review and interpret in-process and finished product analytical results
- Ensure compliance with GMP, GLP, and regulatory requirements
- Identify quality trends, risks, and recurring laboratory issues
- Approve or reject materials and products based on analytical outcomes
- Audit and monitor manufacturing and QC processes for compliance
- Review and approve analytical data, COAs, and laboratory documentation
- Lead investigations of deviations, OOS/OOT, and non-conformances
- Drive CAPA effectiveness and continuous improvement initiatives
- Prepare teams for internal, external, and regulatory audits
- Mentor, develop, and manage QC laboratory leadership teams
Additional Responsibilities:
- Responsible for the operation & calibration of balances in Sampling room & to maintain its record.
- Master Degree (MS/MA) M. Sc. - Required
- M. Pharm M. Pharm - Preferred
- 15 years or more in 15+ Years