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
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
Purpose: The company requires the services of a highly competent and experienced Regulatory Affairs Scientist for the Regulatory Affairs Department Key Job Outputs: Compilation and update of documents to be submitted to regulatory authorities, this includes the compilation of Common Technical Docume
Purpose: The company requires the services of a highly competent and experienced Regulatory Affairs Scientist (Development and Technical Support) for the Regulatory Affairs Department Key Job Outputs: Compilation and/ or update of manufacturing and cleaning instructions according to internal procedu
Purpose: The company requires the services of a highly competent and experienced Regulatory Affairs Scientist for the Regulatory Affairs Department Key Job Outputs: Compilation and update of documents to be submitted to regulatory authorities, this includes the compilation of Common Technical Docume
Purpose: The company requires the services of a highly competent and experienced Regulatory Affairs Scientist (Development and Technical Support) for the Regulatory Affairs Department Key Job Outputs: Compilation and/ or update of manufacturing and cleaning instructions according to internal procedu