Description
Job Purpose: To supervise the manufacturing of solid dosage forms (tablets, capsules) ensuring full compliance with GMP requirements, achieving production targets, and maintaining product quality, safety, and efficiency throughout all production stages Duties & Responsibilities: Supervise dispensing, granulation, blending, compression, coating, and encapsulation processes. Ensure production activities are executed according to approved SOPs and BMRs. Monitor critical process parameters (CPPs) such as blending time, compression force, coating parameters. Verify line clearance before starting any batch activity. Ensure proper documentation of all production activities in batch records and logbooks. Review Batch Manufacturing Records (BMR) for completeness and accuracy. Maintain environmental conditions (temperature, humidity, differential pressure) within limits. Ensure compliance with GMP, hygiene, and safety standards in production areas. Investigate and report deviations, incidents, and non-conformities and participate in CAPA implementation. Coordinate with QA, QC, and Engineering for smooth production operations. Ensure proper cleaning and sanitation of equipment and production areas. Participate in validation activities (process validation, cleaning validation). Monitor equipment performance and report any malfunction or maintenance needs. Optimize production processes to improve yield, reduce waste, and increase efficiency. Ensure adherence to production schedules and achieve planned targets. Train and supervise operators on SOPs, GMP, and safety practices. Job Location: Bady City, Cairo Qualifications: Bachelor's degree in pharmacy or science. From 0:2 years of experience in pharmaceutical manufacturing