Cipla: Regulatory Affairs Compliance Pharmacist - South Africa
Requirements Bachelor of Science Degree and registration with the SAPC A minimum of 2 years’ experience in a healthcare regulatory affairs environment Regulatory Affairs Compliance experience Pharmacovigilance training and experience Preferred Qualifications/experience – CMC training/experience – Risk Manager – Training skills Duties & Responsibilities This individual is responsible to perform all activities pertaining to Chemistry Manufacturing and Controls (CMC) and regulatory affairs compliance aspects pertaining to Cipla SA. You will be expected to liaise with internal departments and business units, associated companies (manufacturers, packers, laboratories and printers) and the strategic regulatory affairs team (Group Head: Regulatory Affairs, Responsible Pharmacists, Risk Committee, Quality Assurance and Regulatory Affairs Managers) on all aspects of CMC and Regulatory affairs compliance. You will also be expected to serve in a key capacity for all Pharmacovigilance activities. Responsibilities include ensuring continued adherence to regulations, auditing and monitoring of documentation, management of the life cycle of all product dossiers, pharmacovigilance, managing product complaints and supporting of and participating in the Corporate Compliance Program. Job Type Classification Permanent Equity Status EE Preferred Location – Country South Africa Location – Province Western Cape Location – Town / City Bellville Department Regulatory Overview CMC and Regulatory Affairs Compliance Pharmacist Click here to apply online
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