Monitor Supervise adherence to Standard Operating Procedures (SOPs), Work Instructions (WIs), and other operational guidelines within the Production product activities to ensure that process parameters are maintained within defined standards.
Analyze and follow up on in-process quality control results to ensure product integrity.
Ensure the consistent implementation of Good Manufacturing Practices (GMP/CPKB) across all stages of the production process.
Coordinate investigations into production deviations, out-of-specification results, customer complaints, and other quality-related issues.
Develop and oversee the execution of Corrective and Preventive Actions (CAPA) to address identified issues.
Review Batch Manufacturing Records (BMRs) prior to submission for batch release.
Lead, train, and supervise the Analyst team within the manufacturing area to ensure high performance and continuous development.
Support technical verification and validation activities prior to formulation transfer to production or third-party manufacturing.
Requirements :
Bachelor’s degree in Pharmacy, Chemistry, Chemical Engineering, or related field
Minimum 3-5 years experience in QA/QC Manufacturing or related functions
Experience in FMCG / Personal Care / Cosmetics industry preferred
Strong knowledge of GMP / CPKB and manufacturing quality systems
Understanding of production processes, critical parameters, and in-process controls
Ability to review and assess BMRs, deviations, OOS, and investigations
Knowledge of CAPA, risk assessment, and root cause analysis tools
Ensure consistent implementation of SOPs and WIs on the production floor
Ability to handle customer complaints and internal quality issues
Familiar with validation & verification activities related to manufacturing
Ability to lead, coach, and supervise Analysts / QA leader
Strong coordination with Production, QC, and Engineering
Good communication and problem-solving skills
#LI-BR1
Dare to be bold, Discover what’s possible, and Do the incredible.