Tiger Brands Limited, a Top 40 JSE Limited company whose footprint extends across the African continent and beyond, is one of the largest manufacturers and marketers of FMCG products in Southern Africa, and has been for several decades.
Tiger Brands has been built over many decades through the acquisition and clustering of businesses. Our strategy for succe...
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As the Responsible Pharmacist you are to perform the duties as contemplated in Regulation 23 (3) of the Pharmacy Act No 53 of 1974 and the relevant sections of the Medicines and Related Substances Act, No 101 of 1965. You will ensure that product quality is maintained at all times by making sure that standard operating practices relating to development, production, laboratory, storage, distribution and vendor approval are adhered to at all times.
Be responsible for quality assurance and form an integral part of the decision making process in all areas affecting the quality of the product.
Develop and maintain a robust quality management system through continuous monitoring and improving of the system within Tiger Brands as well as at contract packers in line with regulatory guidelines.
Co ordinate all recall activities as per regulatory requirements, MCC guidelines and company procedures.
Ensure all registered product dossiers are in compliance with the current requirements of the respective medicines regulatory authority.
Ensure all master documentation is in compliance with the related registered product dossier and ensure amendments are efficiently allocated, a quality submission is prepared and that the submission is tracked to reflect the status of the amendment and/or change. Once approve the dossier will be updated and superseded to reflect the approved amendments.
Manage the medicinal stability programme in line with regulatory guidelines
Carry out annual product reviews and conduct self inspections and quality audits of vendors and contractors
Authorise all packaging, advertising and promotional material and promotional activities relating to scheduled products in compliance with relevant legislation.
Provide input into pharmaceutical perspective of medicinal project viability studies, technical agreements, new product development, formulation and amendments.
Manage the product development and substantiation testing carried out by external research parties
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