Drug Regulatory Affairs Manager Jobs in Gauteng
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Regulatory Affairs Manager Johannesburg
Mvg Recruitment Specialists
Johannesburg
Regulatory Affairs Manager Industry: Pharmaceutical Location: JHB Equity Requirement: EE Lead the Regulatory ensure legal compliance with the relevant medicine Regulatory Authorities (Country Specific where applicable) ensuring timeous processing of regulatory applications. Key Responsibilities: Manage work streams for- and report other MRA's and third-party stakeholders Review regulatory agency submission of materials to ensure timelines accuracy, comprehensiveness, or compliance with regulatory standards Co-ordination and submission of new
share this job on whatsappRegulatory Affairs Pharmacist Gauteng
Mna RecruitmentGauteng
Senior Regulatory Pharmacist. Job Purpose: Support the Regulatory team to provide superior Regulatory services to control and manage a portfolio of product outputs. To ensure legal and regulatory compliance with with the relevant medicine Regulatory Authorities (Country Specific where applicable), Medicines and Related ensuring timeous processing of regulatory applications. Key Responsibilities: Manage work streams for- and report stakeholders Establish regulatory priorities and allocate resources and workloads Review regulatory agency submission
Regulatory Affairs Pharmacist Midrand
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
Regulatory Affairs Scientist Johannesburg
Mvg Recruitment SpecialistsJohannesburg
Regulatory Affairs Scientist Industry: Pharmaceutical Location: JHB Equity Requirement: EE Large Pharmaceutical employ a Regulatory Affairs Scientist. The following applies: Key Responsibilities: Managing and coordinating applications. Managing and coordinating response to the regulatory authority. Maintain regulatory knowledge is required. Effectively managing, auditing and implementation of Regulatory systems Key Requirements: field Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines
Regulatory Affairs Pharmacist Centurion
Futurelink Global RecruitmentCenturion
looking for a Regulatory Affairs/Quality Assurance Pharmacist to join their team. Regulatory Affairs (RA): Submit Assurance (QA): Assist QA Manager with artwork review and quality management system for Act 101 products release of Act 101 products in the absence of QA Manager and RP/Deputy RP. Review and update SOPs and Technical
Head Of Regulatory Affairs
Johannesburg
Monthly
A minimum of 8 years of pharmaceutical regulatory experience is a prerequisite with excellent knowledge
ensure legal compliance with the relevant Health Regulatory Authorities (Country Specific where applicable
relevant regulations in Africa.
Experience with regulatory authorities in sub-Saharan Africa and French
advantageous
Significant experience of regulatory drug development, manufacture, commercialisation
equivalent.
Knowledge of regulatory procedures and legislation for drug development, product registration
Regulatory 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 Waltloo, Pretoria
Alec Cameron & Associates Recruitment SolutionsSouth Africa
the compliance of pharmaceutical products with regulatory requirements in South Africa and other designated designated markets. This role involves managing regulatory submissions, writing and reviewing Chemistry, Manufacturing up-to-date knowledge of regulatory guidelines. Key Responsibilities: 1. Regulatory Submissions: Prepare Prepare, compile, and submit regulatory dossiers for new product registrations, renewals, and variations to Products Regulatory Authority (SAHPRA) and other relevant authorities. Manage timelines for regulatory submissions
Regulatory Affairs Pharmacist Cape Town
Specialist Search RecruitmentSouth Africa
R1 million+, negotiable 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
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
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