Production Manager Quality Manager Jobs in South Africa
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Scientific / QA
- Mna Recruitment
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Ra Pharmacist Gauteng
Mna Recruitment
Gauteng
business support. Provide regular feedback to the RA Manager and cross functional team and marketing teams on the regulatory submission progress of specific products and ensure support needed to drive performance of delay emerge. Proactively identify issues and manage risk, taking appropriate action as required on identify and drive ongoing improvements. Quantity and Quality: Achievements of timely submission and approvals Labelling and Artwork Management Robust Health Authority interactions To track and manage all GRP activities
share this job on whatsappRegulatory Affairs Pharmacist Gauteng
Mna RecruitmentGauteng
and Principals, and to control and manage a portfolio of product outputs. To ensure legal and regulatory Responsibilities: Manage work streams for- and report on the assigned portfolio of products: Assisting with with internal product queries from relevant departments Assisting with external product queries from the standards Co-ordination and submission of new product applications in South Africa and other applicable plans for the preparation and submission of new products Conduct dossier due diligence to ensure all data
Head Of Regulatory Affairs Gauteng
Mna RecruitmentGauteng
commercialisation and life cycle management of the assigned product(s) in product teams. Applies knowledge of Responsible for the management of a skill group such as CMC, Regulatory affairs project management, etc. Responsible Responsible for skill development, performance management, and resource allocation. Key Responsibilities: regulatory agencies and trade associations on product and legislative development issues and monitors Provides strategic regulatory advice support for product developments regional therapy area Represents the
Head Of Regulatory Affairs, African Cluster
Mna RecruitmentGauteng
commercialisation and life cycle management of the assigned product(s) in product teams. Applies knowledge of Responsible for the management of a skill group such as CMC, Regulatory affairs project management, etc. Responsible Responsible for skill development, performance management, and resource allocation. Key Responsibilities: regulatory agencies and trade associations on product and legislative development issues and monitors Provides strategic regulatory advice support for product developments regional therapy area Represents the
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