Regulatory Affairs Manager Industry: Pharmaceutical Location: JHB Equity Requirement: EE Lead the Regulatory regulatory applications. Key Responsibilities: Manage work streams for- and report on the assigned group new products Formulate or implement regulatory affairs systems, policies and procedures to ensure that Council Minimum of 5 years' experience in Regulatory Affairs, preferably in human medicines. Demonstrated experience application will be an advantage. Sound project management capabilities Proven ability to consistently deliver
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Regulatory Affairs Manager (POS24277)
Regulatory Affairs Manager (POS24191)
Area: Aeroton
R1 external partners and Principals, and to control and manage portfolio and team outputs. To ensure legal compliance Council
Key Job Outputs
external partners and Principals, and to control and manage portfolio outputs. To ensure legal compliance with Council
over 5000 clients Reporting to Head: Regulatory Affairs Job purpose: Support the Regulatory team to provide external partners and Principals, and to control and manage portfolio and team outputs. To ensure legal and Council Minimum of 5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrable experience commercialization and maintenance lifecycle Sound project management capabilities Proven ability to consistently deliver quality, time and cost standard Key Job Outputs Manage work streams for- and report on the assigned group
experienced and open-minded Student Regulatory Affairs Manager to join our esteemed campus in Cape Town. This with a strong background in higher education and management to ensure compliance with all regulatory requirements Serve on the Academic Exco team. Manage the regulatory and student affairs team and budget. Lead a small issues. Maintain the Internal Quality Assurance Management system and quality assurance processes. Serve like the Student Information System and Learner Management System. Oversee the production of academic transcripts
competent and experienced Regulatory Affairs Scientist for the Regulatory Affairs Department Key Job Outputs: Pharmaceutical Ingredients (APIs) Responding to customer (both internal and external) and regulatory authority ability to interact well with internal and external customers Minimum of 3years experience in pharmaceutical
external Partners and Principals, and to control and manage a portfolio of product outputs. To ensure legal regulatory applications. Key Responsibilities: Manage work streams for- and report on the assigned portfolio stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that Pharmacy Council -5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrable experience commercialization and maintenance lifecycle Sound project management capabilities Proven ability to consistently deliver
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 stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that Council 3 to 5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrable experience commercialization and maintenance lifecycle Sound project management capabilities Proven ability to consistently deliver
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 compilation and submission of new product applications. Managing and coordinating response to the regulatory authority registration process is required. Effectively managing, auditing and implementation of Regulatory systems Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines Demonstrable