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
experienced Regulatory and Quality Assurance Pharmacist to join their company Job Requirements 2 to 3 years 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
an opportunity for an experienced RA Pharmacist (2 years of RA dossier compilation experience) to join 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 Pharmacy Council (SAPC) is essential Minimum of 2 years Regulatory Affairs experience in pharmaceutical industry
Regulatory Affairs Pharmacist OTC POS24203
Based: Midrand Pharmacy Council
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 -POS24206
Area : Pharmacy Council
Key Job Outputs
Do you consider yourself an expert with Group Reporting and Consolidations? Are you looking for career article experience in a reporting role Statutory Reporting Consolidations JSE reporting, Stakeholder liaison liaison and management Africa experience IFRS compliance and implementation of amended / new standards Preparing Preparing monthly and annual financial statements Manage full internal controls Maintain stakeholder interface
experience in a reporting role
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
experienced Regulatory and Quality Assurance Pharmacist to join their company Job Requirements 2 to 3 years 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