compliance with the OHS Act 85 of 1993 and COID Act. Accountable to providing sustainable OHS support to the sites Environmental Act, and limited exposures. To be accountable for the maintenance of the environmental program staff and relevant staff training is conducted. Accountable to ensure that these safety risks are adequately producing reports. 2 -3 years OHS functional work experience. Excellent knowledge of legislation & procedure OHS/NOSA Audit system. Business financial acumen. Experience with writing policies and procedures for health
compliance with the OHS Act 85 of 1993 and COID Act. Accountable to providing sustainable OHS support to the sites Environmental Act, and limited exposures. To be accountable for the maintenance of the environmental program staff and relevant staff training is conducted. Accountable to ensure that these safety risks are adequately producing reports. 2 -3 years OHS functional work experience. Excellent knowledge of legislation & procedure OHS/NOSA Audit system. Business financial acumen. Experience with writing policies and procedures for health
Degree: Science/ Medical / Biological/ Technical Experience required Advanced Computer Skills (MS Office {Non-Negotiable} 2-5 Years working experience in the Medical Industry {Preferable} Experience with data collection collection and trending Experience with Quality Management Systems ISO 13485 or ISO 9001 or any other ISO standard (Preferred) Experience with Regulatory Affairs and understanding of regulations (Preferred) Experience with
Degree: Science/ Medical / Biological/ Technical Experience required Advanced Computer Skills (MS Office {Non-Negotiable} 2-5 Years working experience in the Medical Industry {Preferable} Experience with data collection collection and trending Experience with Quality Management Systems ISO 13485 or ISO 9001 or any other ISO standard (Preferred) Experience with Regulatory Affairs and understanding of regulations (Preferred) Experience with
years' experience in Regulatory Affairs, preferably in human medicines Demonstrable experience across consistently deliver to quality, time and cost standards Experience in use of CTD software builder and compilation
years' experience in Regulatory Affairs, preferably in human medicines Demonstrable experience across consistently deliver to quality, time and cost standards Experience in use of CTD software builder and compilation
join their company Job Requirements 2 to 3 years experience in compilation and submission of Act 101 dossiers dossiers submissions CTD submission experience Vet industry experience Knowledge of regulatory submissions
join their company Job Requirements 2 to 3 years experience in compilation and submission of Act 101 dossiers dossiers submissions CTD submission experience Vet industry experience Knowledge of regulatory submissions
Field Matric is a minimum requirement 1 Years Experience in quality assurance or regulatory affairs in
Field Matric is a minimum requirement 1 Years Experience in quality assurance or regulatory affairs in