M&L Laboratory Services (Pty) Ltd (part of the Bureau Veritas Group of Companies) is recruiting a QC/QA Coordinator based in Ormonde (Johannesburg) to perform quality control and reporting to the Quality Manager. and to ensure full compliance to ISO 17025 as well as ensuring OECD GLP requirement
Reference: DBN003540-SS-3 A Leading Pharmaceutical Company has a vacancy for a Senior Regulatory Pharmacist. Job Purpose: Support the Regulatory team to provide superior Regulatory services to relevant departments within the company and with external Partners and Principals, and to control and manag
M&L Laboratory Services (Pty) Ltd (part of the Bureau Veritas Group of Companies) is recruiting a QC/QA Coordinator based in Ormonde (Johannesburg) to perform quality control and reporting to the Quality Manager. and to ensure full compliance to ISO 17025 as well as ensuring OECD GLP requirement
BSc in Food Science. 2 years' relevant experience in the food industry. Willing to travel. Valid driver's license. Location: Cape Town/Gauteng/George Description: A leading provider of innovative and high-quality equipment solutions for the meat processing industry requires a Product Application S
SHEQ Management: • SHEQ management and security of the entity: • Conduct internal Audits and inspections. • Conduct HIRA and put control measures in place. • Develop and implement SOP/ WI. • Conduct Incident Investigation • Attend to all IOD and COD claims • Arrange for all SHEQ traini
SHEQ Management: • SHEQ management and security of the entity: • Conduct internal Audits and inspections. • Conduct HIRA and put control measures in place. • Develop and implement SOP/ WI. • Conduct Incident Investigation • Attend to all IOD and COD claims • Arrange for all SHEQ traini
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 main job purpose is to ensure the compliance of pharmaceutical products with regulatory requirements in South Africa and other designated markets. This role involves managing regulatory submissions, writing and reviewing Chemistry, Manufacturing, and Controls (CMC) documentation, and maintaining
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
Our Client, based in Centurion, is looking for a Regulatory Affairs/Quality Assurance Pharmacist to join their team. Regulatory Affairs (RA): Submit new dossiers for health products to authorities in South Africa and other markets (Namibia, Botswana, Zambia, etc.). Liaise with contract manufacturers