Hiring Assistant Manager For QC - Analytical Method Validations

Role & responsibilities

• Perform Analytical Method Validation (AMV).
• Handle HPLC, UPLC, GC, and Dissolution analysis.
• Review validation documents and reports.
• Investigate OOS/OOT and implement CAPA.
• Ensure GMP, GLP, and Data Integrity compliance.

Preferred candidate profile

• Considering Only QC Exp- Candidates
• M.Sc. / M.Pharm / B.Pharm.
• 10-13 years of experience in QC Formulations.
• Hands-on experience in Method Validation and HPLC/UPLC.
• Good knowledge of GMP and regulatory guidelines.
• Strong communication and team management skills.