Drug Regulatory Affairs Manager Jobs in Midrand, Gauteng
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Regulatory Affairs Pharmacist Midrand
Mvg Recruitment Specialists
Midrand
Senior Regulatory Affairs Pharmacist Industry: Pharmaceutical Location: Midrand Equity Requirement: EE EE Key Responsibilities: Manage work streams for- and report on the assigned portfolio of products Conduct with Regulatory Authorities, internal and external stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that regulatory compliance is maintained or enhanced. Key Requirements: Pharmacy Council 3 to 5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrable
share this job on whatsappRegulatory Affairs Pharmacist Midrand
Specialist Search RecruitmentSouth Africa
R800k to R1 mil, negotiable based on experience submissions . Activities relating to product lifecycle management. Maintain and develop working relationships effectively effectively and provide required regulatory support. Reviewing artwork relating to products ensuring abreast of developments and changes in the local regulatory environment which directly impacts on the product Council (SAPC) is essential Minimum of 2 years Regulatory Affairs experience in pharmaceutical industry . Experience Experience working with SAHPRA and other Regulatory Authorities in Africa. Excellent spoken and written
Regulatory Affairs Pharmacist - Otc
Midrand
R750k - 800k per year
Regulatory Affairs Pharmacist OTC POS24203
Based: Midrand Council
Key Job Outputs
- Manage work streams for- and report on the assigned portfolio tablish regulatory priorities and allocate resources and workloads
- Review regulatory agency submission
Pharmacist Regulatory Affairs Midrand, Jhb
Specialist Search RecruitmentSouth Africa
R100k ctc p/m plus guaranteed 13th cheque (neg). pharmaceutical sector has an opportunity for an RA Manager to lead their team. You need 5 years of RA experience to step up into an RA Manager role. This role is more about project management. Ensure that the RA team monthly work output targets. Primarily you will be managing the RA team, rather than compiling dossiers. Although
Senior Regulatory Affairs Pharmacist: Otc
Midrand
R950k - 1,000k per year
Senior Regulatory Affairs Pharmacist: OTC -POS24206
Area : Pharmacy Council
Key Job Outputs
- Manage work streams
Senior Regulatory Affairs Pharmacist (midrand) Market Related
Mvg Recruitment SpecialistsMidrand
Senior Regulatory Affairs Pharmacist Industry: Pharmaceutical Location: Midrand Equity Requirement: EE EE Key Responsibilities: Manage work streams for- and report on the assigned portfolio of products Conduct with Regulatory Authorities, internal and external stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that regulatory compliance is maintained or enhanced. Key Requirements: Pharmacy Council 3 to 5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrable
Senior Regulatory Affairs Pharmacist Complimentary Medicine (cam)
Midrand
R950k - 1,000k per year
Senior Regulatory Affairs Pharmacist Complimentary Medicine (CAM) POS24204
Key Job Outputs
- Manage work streams
Senior Regulatory Affairs Pharmacist: Pain, Derma & Digestive (pdd)
Midrand
R950k - 1,000k per year
Senior Regulatory Affairs Pharmacist: Pain, Derma & Digestive (PDD) - POS24205 Key Job Outputs
Regulatory And Quality Assurance Pharmacist
Masa Outsourcing LtdSouth Africa
PE000998-CP-1 Our client is looking for an experienced Regulatory and Quality Assurance Pharmacist to join their experience Vet industry experience Knowledge of regulatory submissions in Botswana, Nambia, Zambia, Zimbabwe Job Duties Regulatory Affairs Duties Regulatory Submissions: Prepare and submit regulatory documents to comply with regulatory guidelines and requirements. Compliance: Monitor and interpret regulatory requirements international regulations. Product Registration: Manage the process of registering new products or updating
Regulatory Pharmacist Johannesburg - North (sandton / Midrand / Diepsloot)
Masa Outsourcing LtdSouth Africa
PE000998-CP-1 Our client is looking for an experienced Regulatory and Quality Assurance Pharmacist to join their experience Vet industry experience Knowledge of regulatory submissions in Botswana, Nambia, Zambia, Zimbabwe Job Duties Regulatory Affairs Duties Regulatory Submissions: Prepare and submit regulatory documents to comply with regulatory guidelines and requirements. Compliance: Monitor and interpret regulatory requirements international regulations. Product Registration: Manage the process of registering new products or updating
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