Evaluating internal controls and maintenance of cGMP documentation for
compliance with quality and regulatory standards.
Assisting in Training on cGMP across the business.
Participating in Internal and external auditing and following up on action points.
Assisting in the Implementation and review of the documentation system.
Implementation of investigations, Complaints, and Recall system.
Reviewing of Standard Operating Procedures, Monographs, Protocols, and Specifications.
Supervision and Management of Quality Assurance staff.
Oversight of Equipment Qualification, Utilities, Cleaning, Analytical Method, and Process Validation activities.
Qualifications and Experience
The ideal candidate should be analytical and proficient in all aspects of the Quality
Management Systems procedures, with the following qualifications and experience
A Bachelor of Pharmacy degree
A minimum of two year’s experience in a pharmaceutical manufacturing environment.
Valid practising certificate from Pharmacists Council of Zimbabwe ( PCZ).
Substantial knowledge of Quality Management Systems as applicable in the pharmaceutical industry (cGMP) and the associated regulatory bodies guiding the pharmaceutical industry.