The purpose of this position is to ensure cGMP compliance, and assess, authorize, and oversee all Quality Assurance initiatives of SA and overseas 3rd party and Contract manufacturers. General QA functions, specifically leaning toward QA oversight of 3rd party & Contract manufacturers (SA and international): Reviewing and approval of all master production and quality documentation . Compile and review SOPs. Participate in audits on contract manufacturers . Change controls and deviations . CAPAs initiated at contract manufacturers relating to manufacturing, customer complaints, stability, OOS, and recalls. Monitors validation and technical transfer batches at contract manufacturers. QA release . Product/process queries . Participate in projects, product launches, and product transfers . Manage the stability schedule and process for products manufactured at contract manufacturers. Conducts quality reviews of operations at contract manufacturing sites . B.Pharmacy; cGMP skills Computer literacy: MS Office 3 years in pharmaceutical manufacturing environment 2 -3 years quality assurance experience - preferably with 3rd party manufacturers too This role has a broad salary range. Salary is affected by specific industry skills relevant to this position, specific relevant qualifications and courses, the number of years in the pharmaceutical sector, the number of years in a QA environment, the number of years working with 3rd party suppliers and external contract suppliers, specific software skills, and other relevant factors. A salary range of R60k to R70k p/m plus a guaranteed 13th cheque is envisaged for this role - negotiable. (About R800k to R900k as a total package). Apply Now

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