Job Description
Notifies all involved departments of all rejects or other non-conforming results related to raw material, packaging material, finished products, water testing and any other area monitored by QC testing.
Develops and updates Quality policies and systems, Promote quality achievement and performance improvement throughout the organization
Increase the QC teams awareness in the drug manufacturing process by establishing internal and external training programs that shall target critical areas to ensure integration of quality in every production function
Increase the QC teams awareness in the drug manufacturing process by establishing internal and external training programs that shall target critical areas to ensure integration of quality in every production function.
Ensuring tests and procedures are properly understood, carried out and evaluated and that product modifications are investigated if necessary, Identifying relevant quality-related training needs and delivering training
Facilitate and support quality management in all quality activities, work with the head of the Quality Unit and the Operations managers with the goal of producing a quality product at the lowest possible cost.
Performs periodical employee appraisal for subordinates. Investigate all manufacturing process problems and product failures to meet with its specifications and manufacturing process requirements at the manufacturing site
Assessing the product specifications of the company and its suppliers, and comparing with pharmacopoeia and in-house specifications.
Reviews and approves SOPs, specification sheets and MOAs
Reviews and evaluates all data generated by QC laboratories and accordingly accepts/rejects raw material, packaging material and finished products through review and approval of analysis reports and COAs
Approves Installation/Operation and Performance Qualification protocols and reports, reviews and approves Process Validation protocols and reports
Ensures integrity and traceability of all data generated
Makes sure that required safety instructions are fully implemented, ensures that waste treatment is carried out according to up-to-date regulations, ensures that all standards, reagents, solvents and other chemicals are properly prepared, maintained and used
Any other task assigned by the supervisor.
Job Specification
Candidate should be; Pharmacist / Pharm-D / M Sc (Chemistry), with 4-5 years experience in similar capacity with multinational company, age: 35 to 45 years, fully computer literate, salary: negotiable.