An established manufacturing company is upgrading their facility to be GMP compliant for SAHPRA audits. They would like to implement ISO standards too. Manufacturers of pharma, cosmetics, and medical device products. Initially, the primary functions will be to ensure GMP compliance across the small/
An established manufacturing company is upgrading their facility to be GMP compliant for SAHPRA audits. They would like to implement ISO standards too. Manufacturers of pharma, cosmetics, and medical device products. Initially, the primary functions will be to ensure GMP compliance across the small/
The company is an established leader in the pharmaceutical sector, with over 90 products, many of them 'famous-brand' and 'Blockbuster' products in the CAMS, cosmetics, and medical devices sector. They export to over 60 countries. In particular, this position will require input into RA requirements
The company is an established leader in the pharmaceutical sector, with over 90 products, many of them 'famous-brand' and 'Blockbuster' products in the CAMS, cosmetics, and medical devices sector. They export to over 60 countries. In particular, this position will require input into RA requirements
An established manufacturing company is upgrading their facility to be GMP compliant for SAHPRA audits. They would like to implement ISO standards too. Manufacturers of pharma, cosmetics, and medical device products. Initially, the primary functions will be to ensure GMP compliance across the small/
A leading pharmaceutical company has an opportunity for an experienced RA Pharmacist (2 years of RA dossier compilation experience) to join their team. Compile and submit new product applications and ensure that the registration requirements are fulfilled so that the registration process and approva
A leading pharmaceutical company has an opportunity for an experienced RA Pharmacist (2 years of RA dossier compilation experience) to join their team. Compile and submit new product applications and ensure that the registration requirements are fulfilled so that the registration process and approva
An established pharmaceutical manufacturing company has an opportunity for two Validation Analysts to join their team. Ideally, one more experienced analyst (3 to 4 years' experience), and one more junior analyst (1 to 2 years of experience). This position will report to the QC (Quality Control) Man
An established pharmaceutical manufacturing company has an opportunity for two Validation Analysts to join their team. Ideally, one more experienced analyst (3 to 4 years' experience), and one more junior analyst (1 to 2 years of experience). This position will report to the QC (Quality Control) Man
An established pharmaceutical manufacturing company has an opportunity for two Validation Analysts to join their team. Ideally, one more experienced analyst (3 to 4 years' experience), and one more junior analyst (1 to 2 years of experience). This position will report to the QC (Quality Control) Man