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
