- Perform and review analysis of Raw Materials, Finished Products, In-Process Samples, and Stability Samples.
- Operate and troubleshoot analytical instruments such as HPLC, GC, UV, IR, Dissolution, and other laboratory equipment.
- Review analytical data, test reports, and laboratory documentation.
- Ensure compliance with cGMP, GLP, SOPs, STPs, and regulatory requirements.
- Investigate OOS, OOT, deviations, and laboratory incidents.
- Prepare and review analytical reports, specifications, and protocols.
- Coordinate with QA, Production, and other departments for quality-related activities.
- Support method validation, method transfer, calibration, and stability studies.
- Participate in internal audits, customer audits, and regulatory inspections.
Qualification
- B.Pharm / M.Pharm / M.Sc (Chemistry) or equivalent.
Experience
- Minimum 5 years of experience in Quality Control within a pharmaceutical manufacturing company.
Skills
- Hands-on experience with HPLC, GC, UV, IR, and Dissolution.
- Knowledge of cGMP, GLP, Data Integrity (ALCOA+), and regulatory requirements.
- Documentation review and investigation handling.
- Strong analytical, communication, and team management skills.
Pay: ₹200,000.00 - ₹400,000.00 per year
Work Location: In person
