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Assistant QC Manager – Pharmaceuticals

Sagar Vitaceuticals Nigeria Limited | Ogun, Nigeria

Full-time Posted 1 day ago 1 view

About the Role

Sagar Vitaceuticals Nigeria Limited, a leading name in the Nigerian pharmaceutical industry known for trusted brands like Vitaclox and Vitacillin, is looking for a dedicated Assistant QC Manager to join our ultra-modern manufacturing facility in Ikeja, Lagos. In this pivotal role, you will play a crucial part in maintaining our high standards of product excellence, safety, and regulatory compliance.

Key Responsibilities
  • Supervise day-to-day quality control activities covering raw materials, packaging materials, in-process goods, finished products, and stability samples.
  • Review and approve analytical test results, Certificates of Analysis (COAs), worksheets, and essential laboratory documentation.
  • Ensure all testing procedures strictly adhere to approved specifications, SOPs, pharmacopoeial standards, and Good Manufacturing Practices (GMP).
  • Lead investigations for Out-of-Specification (OOS), Out-of-Trend (OOT), deviations, and laboratory incidents while implementing robust Corrective and Preventive Actions (CAPA).
  • Oversee the proper operation, calibration, qualification, and maintenance of advanced laboratory instruments including HPLC, GC, UV-Vis, and FTIR.
  • Maintain stringent laboratory compliance with GLP, data integrity, and local or international regulatory standards.
  • Coordinate seamlessly with QA, Production, R&D, and Regulatory Affairs to resolve quality-related challenges.
  • Train, mentor, and supervise QC analysts while enforcing strict laboratory safety protocols.
  • Participate actively in internal audits, customer audits, and regulatory agency inspections.
Qualifications
  • Bachelor of Pharmacy (B.Pharm), Master of Pharmacy (M.Pharm), B.Sc. or M.Sc. in Chemistry, or a related analytical science discipline.
  • 4 to 10 years of hands-on pharmaceutical quality control experience, with proven supervisory or team-lead capability.
  • Strong working knowledge of GMP, GLP, pharmacopoeias, advanced analytical techniques, and data integrity principles.
  • Familiarity with regulatory expectations from WHO-GMP, USFDA, MHRA, or NAFDAC is a distinct advantage.
Benefits
  • Competitive salary package commensurate with experience and industry standards.
  • Comprehensive health insurance and medical benefits for employee and dependents.
  • Opportunities for professional development and career advancement within a leading pharmaceutical manufacturer.
  • Dynamic, collaborative work environment in a state-of-the-art facility located in Ikeja, Lagos.

Skills

Quality Control GMP GLP HPLC OOS Investigations Data Integrity Pharmaceutical Analysis Supervision CAPA
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