Job Openings - Mersifarma

Supervisor QC WIP & FG

Supervise analytical testing activities for Work In Process (WIP), bulk products, and Finished Goods (FG).
Lead and develop QC Analysts to ensure testing activities are conducted in accordance with approved procedures and GMP/CPOB requirements.
Review analytical records, laboratory documentation, and test reports to ensure accuracy and compliance.
Monitor laboratory operations, including logbooks, controlled substances, working standards, and analytical equipment utilization.
Investigate deviations, OOS/OOT results, and support CAPA implementation.
Collaborate with Production, QA, and other stakeholders regarding product quality and testing status.
Review and improve analytical methods, SOPs, and laboratory practices.
Prepare periodic reports and support internal/external audits and regulatory inspections.
Ensure compliance with safety, environmental, and quality management requirements.

Bachelor's Degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or related fields.
Pharmacist (Apothecary) certification is an advantage.
Minimum 5 years of experience in Pharmaceutical Quality Control, with prior supervisory experience preferred.
Strong understanding of GMP/CPOB, Deviation Management, CAPA, Validation, Qualification, Calibration, Risk Management, and Internal Audit Systems.
Hands-on experience with analytical instruments such as: HPLC, GC, UV-Vis Spectrophotometer, FTIR, Karl Fischer, ICP-OES, Dissolution Tester, and other laboratory analytical equipment.
Strong leadership, communication, teamwork, and problem-solving skills.
Proficient in Microsoft Office applications.