Manager - QC Chemist
1 Nos.
130518
Full Time
9.0 Year(s) To 11.0 Year(s)
8.00 LPA TO 10.00 LPA
Production / Quality / Maintenance
Pharma/Biotech/Clinical Research
B.Sc - Chemistry; M.Sc / MS Science - Chemistry; M.Sc / MS Science - Organic Chemistry
Job Description:
Key Responsibilities:
- Manage and oversee all Quality Control activities for formulation products.
- Ensure compliance with cGMP, GLP, and regulatory guidelines.
- Review and approve analytical reports, COA, STP, and specifications.
- Handle instrument operations like HPLC, GC, UV, Dissolution apparatus, etc.
- Ensure calibration, validation, and maintenance of QC instruments.
- Coordinate with QA, Production, and R&D for smooth operations.
- Handle OOS, OOT, deviations, and CAPA investigations.
- Ensure timely testing of raw materials, in-process, and finished products.
- Prepare and review SOPs, protocols, and reports.
- Lead audits (internal, external, regulatory) and ensure compliance readiness.
Desired Profile / Criteria / Skills :
Required Skills:
- Strong knowledge of analytical techniques (HPLC, GC, UV)
- Good understanding of regulatory guidelines (WHO, USFDA, MHRA)
- Leadership and team management skills
- Strong documentation and investigation skills
- Problem-solving and decision-making ability
Company Profile
Our client followa standards of WHO - CGMP
Our Mission
“To become a valued Pharmaceutical partner to the World Pharma fraternity by continuously researching, developing and manufacturing a wide range of pharmaceutical products that complies with the global regulatory standards.”
Apply Now
- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.