Summary of Responsibilities
Ensuring all production activities strictly follow GMP guidelines and regulatory requirements to guarantee product safety and quality.
Supervising daily manufacturing operations (e.g., dispensing, granulation, compression, coating, filling, packaging) to meet production targets.
Ensuring accurate completion of batch manufacturing records (BMR), batch packaging records (BPR), logbooks, and other documentation in line with regulatory standards.
Working closely with QA/QC teams to ensure in-process checks, line clearance, and product quality standards are maintained.
Ensuring proper line clearance before and after production to prevent cross-contamination and mix-ups.
Overseeing proper use, cleaning, and maintenance of production equipment, and ensuring calibration status is up to date.
Enforcing strict hygiene, gowning procedures, and safety protocols to maintain a controlled production environment.
Identifying, reporting, and documenting deviations, non-conformances, and participating in investigations and CAPA (Corrective and Preventive Actions).
Training operators on SOPs (Standard Operating Procedures), GMP, and safety practices; supervising and evaluating team performance.
Ensuring correct dispensing, storage, and usage of raw materials and packaging materials in line with approved procedures.
Supporting internal and external audits by ensuring documentation and processes are audit-ready at all times.
Academic Qualification and Skills
HND / B.S.c Degree in Industrial Chemistry,Biochemistry or related field.
Minimum of 4 years working experience in pharmaceutical manufacturing or production environment.
GMP (Good Manufacturing Practice) certification
Ability to supervise and motivate staff
Ability to prepare reports and documentation
Ability to meet production targets and deadlines
Critical for ensuring product quality, accuracy in documentation, and compliance
Basic knowledge of systems like ERP, MS Excel, and production tracking tools