Regulatory Affairs Scientist (Development and Technical Support) for the Regulatory Affairs Department Key Job
Purpose: The company requires the services of a highly competent and experienced Regulatory Affairs Scientist for the Regulatory Affairs Department Key Job Outputs: Compilation and update of documents to be submitted to regulatory authorities, this includes the compilation of Common Technical Docume
Purpose: The company requires the services of a highly competent and experienced Regulatory Affairs Scientist for the Regulatory Affairs Department Key Job Outputs: Compilation and update of documents to be submitted to regulatory authorities, this includes the compilation of Common Technical Docume
Regulatory Affairs Scientist (Development and Technical Support) for the Regulatory Affairs Department Key Job
is a must. General Description / Job Purpose: Supports the ED team with managing reporting relating to regarding ED reporting, to receive the ED reports and supporting documentation and to ensure that contractors commitments in detail and vets achievements against supporting documentation. Assists in liaising with company's achievements and supporting documentation (procurement data) as well as supporting documents to substantiate substantiate job creation data. Ensures that all supporting documentation has been collated and saved on
Position Summary: The incumbent is responsible for supporting Pharmacovigilance-related activities in South scope of the role and the countries the role will support, includes, Sub Saharan Africa (Angola, Botswana Therapeutic Areas, and Disease Pathway knowledge supporting the needs of the local Medical and Marketing regulations. Pharmacovigilance-Safety training support: Support LSO/CSTL in the preparation, conduct and timely material, where needed. PV contract management: Support LSO/CSTL with the local Pharmacovigilance Agreements
Position Summary: The incumbent is responsible for supporting Pharmacovigilance-related activities in South scope of the role and the countries the role will support, includes, Sub Saharan Africa (Angola, Botswana Therapeutic Areas, and Disease Pathway knowledge supporting the needs of the local Medical and Marketing regulations. Pharmacovigilance-Safety training support: Support LSO/CSTL in the preparation, conduct and timely material, where needed. PV contract management: Support LSO/CSTL with the local Pharmacovigilance Agreements
Process & systems audit and Issue report. Support SQT to identify and evaluate potential risks and supplier's product quality and process capability. Support Parts and Process approval submission according and release it accurately to Production at SOP. Support formulating incoming product inspection documents training and assessment for inspection personnel. Support SQT in responding quickly to supplier quality problems
Team). • Representative for health and safety • Support SQT and external / internal suppliers to ensure / Customer requirements / VDA6.3 / IATF16949 • Support supplier quality issues and ensure the effective Process & systems audit and Issue report. • Support SQT to identify and evaluate potential risks and supplier's product quality and process capability. • Support Parts and Process approval submission according release it accurately to Production at SOP. • Support formulating incoming product inspection documents