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Quality Control Manager
Job Description & How to Apply Below
We are looking for someone who has grown through core laboratory and QC operations and is comfortable taking end-to-end ownership of the department — from day-to-day laboratory functioning and release timelines to investigations, compliance, team development and regulatory readiness.
Key Responsibilities
Lead the overall Quality Control function covering raw materials, packaging materials, in-process samples, finished products and stability testing
Ensure timely sampling, testing, review and release of materials and products
Manage and review OOS, OOT, laboratory incidents and investigations , ensuring scientifically sound root-cause analysis and CAPA
Oversee stability studies , stability chambers, protocols, data evaluation and related documentation
Ensure appropriate operation, calibration, qualification and maintenance of laboratory instruments including HPLC, GC, UV, FTIR and other QC equipment
Drive laboratory compliance with GMP, GLP, data integrity and good documentation practices
Oversee analytical method validation, verification and method transfer activities
Ensure laboratory documentation, specifications, SOPs, STPs, worksheets and records remain current and compliant
Lead, train and develop QC analysts, officers and managers while improving laboratory productivity and turnaround times
Work closely with QA, Production, Warehouse, Regulatory Affairs and Engineering teams
Support customer audits, regulatory inspections and responses to audit observations
Maintain strong control over laboratory systems, records, reference standards, reagents, columns and consumables
Identify recurring quality issues and drive practical improvements within the laboratory
Candidate Profile
M.Sc. /
B.Pharm / M.Pharm or equivalent relevant qualification
Approximately 12–18 years of progressive experience in pharmaceutical Quality Control
Strong hands-on experience in QC laboratory operations , rather than purely administrative quality roles
Experience managing a QC team and taking independent responsibility for laboratory performance
Strong knowledge of OOS/OOT investigations, stability, analytical instrumentation, method validation/transfer and data integrity
Experience in a GMP-regulated pharmaceutical manufacturing environment is essential
Exposure to USFDA or other regulated-market requirements will be strongly preferred
Experience with topical / external preparations such as creams, ointments, gels, lotions or similar dosage forms will be an advantage
Should be a practical, floor-oriented leader capable of balancing compliance with operational timelines
We are particularly interested in candidates who have spent a substantial part of their career inside the QC laboratory and manufacturing environment and are looking to take comprehensive ownership of the function.
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