Qualification
l M.Sc Chemistry / Analytical Chemistry
l 5–10 years experience in API pharmaceutical industry
l Experience handling HPLC, GC, UV, IR, and wet lab operations, Stability Study.
Key Responsibilities
l Manage overall QC laboratory operations.
l Ensure testing of:
l Raw materials
l Packing materials
l In-process samples
l Finished products
l Stability samples.
l Review and approve analytical reports and COAs.
l Ensure calibration and maintenance of laboratory instruments.
l Supervise HPLC, GC, UV, IR, and wet chemistry analysis.
l Investigate OOS, OOT, CAPA, Change Control and laboratory deviations.
l Prepare and review SOPs, specifications, and STPs.
l Ensure compliance with data integrity and GMP requirements.
l Monitor reference standards and reagent management.
l Coordinate method validation and method transfer activities.
l Train QC staff and analysts.
l Support regulatory and customer audits.
l Ready to work in rotational shifts as per plant and production requirements.
Skills Required
l Strong analytical and troubleshooting skills
l Knowledge of pharmacopoeia and GMP
l Team handling capability
l Knowledge of laboratory investigations and data integrity
Pay: Up to ₹800,000.00 per year
Benefits:
- Cell phone reimbursement
- Flexible schedule
- Health insurance
- Paid sick time
- Paid time off
Ability to commute/relocate:
- Boisar, Thane, Maharashtra: Reliably commute or planning to relocate before starting work (Required)
Education:
Experience:
- in GMP QC: 10 years (Required)
Shift availability:
- Day Shift (Required)
- Night Shift (Required)
- Overnight Shift (Required)
Work Location: In person
