Production Chemical Process Technician Jobs in Gauteng
Ra Pharmacist Gauteng
Mna Recruitment
Gauteng
the regulatory submission progress of specific products and ensure support needed to drive performance Practice (GRP) Ensure that all the regulatory processes are performed timeously and in line with GRP. Maintain GRP standards in the following process areas: Marketing Authorization Applications License License maintenance: Ensure all post-approval product maintenance activities including CMC variations through the Company. Global Labelling Business Process using the GAZELLE system. Co-ordinate the operations
share this job on whatsappRegulatory Affairs Pharmacist Gauteng
Mna RecruitmentGauteng
Principals, and to control and manage a portfolio of product outputs. To ensure legal and regulatory compliance South African Pharmacy Council, ensuring timeous processing of regulatory applications. Key Responsibilities: on the assigned portfolio of products: Assisting with internal product queries from relevant departments departments Assisting with external product queries from the SAHPRA, other MRA's and third-party stakeholders standards Co-ordination and submission of new product applications in South Africa and other applicable
Head Of Regulatory Affairs Gauteng
Mna RecruitmentGauteng
and life cycle management of the assigned product(s) in product teams. Applies knowledge of current local 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 and requirements that impact on new and existing product registrations Ensures effective collaboration across and effective submissions, approvals and other product maintenance activities Participates in skill-development
Head Of Regulatory Affairs, African Cluster
Mna RecruitmentGauteng
and life cycle management of the assigned product(s) in product teams. Applies knowledge of current local 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 and requirements that impact on new and existing product registrations Ensures effective collaboration across and effective submissions, approvals and other product maintenance activities Participates in skill-development
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