We are seeking a dedicated QC Chemist to perform routine analysis, operate analytical instruments, and ensure quality compliance in the manufacturing of API and Bulk Drugs.
Key Responsibilities:
- Analyze raw materials, intermediates, and finished products.
- Operate and maintain instruments like HPLC, GC, UV, IR, and Karl Fischer.
- Prepare and maintain test reports, logbooks, and Certificates of Analysis.
- Ensure adherence to GMP, GLP, SOPs, and regulatory requirements.
- Participate in OOS/OOT investigations and stability studies.
- Support production and QA teams for in-process checks and approvals.
- Maintain calibration of laboratory instruments and lab safety practices.
Requirements:
- Qualification: B.Sc / M.Sc (Chemistry/Pharma), B.Pharm / M.Pharm, Chemical Engineering.
- Fresher or 2-3 years of experience in QC (pharma industry).
- Strong knowledge of analytical techniques and regulatory guidelines.
- Good documentation and problem-solving skills.