Key Responsibilities
· Manage day-to-day operations of the QC Chemical Laboratory.
· Review and approve analytical data, COA, SOPs, STPs, specifications and laboratory documents.
· Ensure compliance with cGMP, GLP, GDP and Data Integrity requirements.
· Handle QMS activities including OOS, OOT, Deviations, CAPA, Change Control and Risk Assessment.
· Oversee qualification, calibration and maintenance of QC instruments (HPLC, GC, UV, FTIR, TOC, pH Meter, Conductivity Meter, etc.).
· Coordinate testing of Raw Materials, Packing Materials, In-process, Finished Products, Stability and Water samples.
· Support internal, customer and regulatory audits.
· Lead, train and develop the QC team while ensuring timely batch release support.
Candidate Requirements
Preferable Experience in Sterile Experience (injectable Plant)
· Qualification: M.Sc. Chemistry / Analytical Chemistry or equivalent.
· Experience: 10–15 years in Pharmaceutical Quality Control (Injectable experience preferred).
· Strong knowledge of cGMP, GLP, Data Integrity and regulatory requirements.
· Hands-on experience with HPLC, GC, UV, FTIR and other analytical instruments.
Good leadership, documentation review and team management skills.
Pay: ₹1,800,000.00 - ₹2,500,000.00 per year
Benefits:
- Health insurance
- Provident Fund
Work Location: In person
