Product Specialist Nutrition Jobs in South Africa
- Limpopo (2)
- North West (2)
- Free State (2)
Scientific / QA
- Mna Recruitment
- Last 7 days (3)
- Last 3 days (2)
Head Of Regulatory Affairs Gauteng NEW
Mna Recruitment
Gauteng
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
share this job on whatsappHead Of Regulatory Affairs, African Cluster NEW
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
Regulatory Affairs Pharmacist Gauteng
Mna RecruitmentGauteng
Principals, and to control and manage a portfolio of product outputs. To ensure legal and regulatory compliance 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 plans for the preparation and submission of new products Conduct dossier due diligence to ensure all data
Ra Pharmacist Gauteng
Mna RecruitmentGauteng
the regulatory submission progress of specific products and ensure support needed to drive performance License maintenance: Ensure all post-approval product maintenance activities including CMC variations submissions, product registration or maintenance throughout the lifecycle of the product is managed effectively line with registration plan. Time to register new products vs. target and vs. industry norm. Extent of compliance non-approval or non-submission of critical variations Product labelling activities successfully completed within
Share on Facebook
Share on Twitter
Share on Linkedin