intensive projects and research. Demonstrated ability to form and work effectively with national and international within 14 days of submitting your application that your application was unsuccessful. However, please
projects and research.
submitting any Personal Information to MPRTC in any form you acknowledge that such conduct constitutes a contacted within 14 days, please consider your application unsuccessful. You have the right to "Opt-Out"
RESPONSIBILITIES • Receives, sorts and refers (where applicable) specimens for testing. • Verifies, capture and received and tests requested on the requisition form. • Carries out different laboratory procedures for etc. • Labels and stores samples/media (where applicable) to ensure traceability in accordance with procedures
RESPONSIBILITIES • Receives, sorts and refers (where applicable) specimens for testing. • Verifies, capture and received and tests requested on the requisition form. • Carries out different laboratory procedures for etc. • Labels and stores samples/media (where applicable) to ensure traceability in accordance with procedures
submitting any Personal Information to MPRTC in any form you acknowledge that such conduct constitutes a contacted within 14 days, please consider your application unsuccessful. You have the right to “Opt-Out”
calculations, reports may be computerised or in hardcopy form. Development of sample preparation methods and implementation advice. Ensure predictability of results by the application of standard procedures. Work must be done without SOP's and other standards are followed, and where applicable apply knowledge and training to work undertaken
calculations, reports may be computerised or in hardcopy form. Development of sample preparation methods and implementation advice. Ensure predictability of results by the application of standard procedures. Work must be done without SOP's and other standards are followed, and where applicable apply knowledge and training to work undertaken
Regulatory Authorities (Country Specific where applicable), Medicines and Related Substances Control Act Council, ensuring timeous processing of regulatory applications. Key Responsibilities: Manage work streams for- submission of new product applications in South Africa and other applicable territories, including but gaps are addressed Prepare the registration applications for submission to the regulatory authorities CTD software builder and compilation of eCTD applications. IT skills Ability to prioritise and work to
follow-up of corrections pertaining to 2.1.2 where applicable. o Registration of samples. o Documenting all reparation and maintenance where relevant and applicable as per protocols, procedures and methods of equipment monitoring of laboratories and equipment in the applicable section. SCHEDULING OF AND SAMPLE PROCESSING assistants (permanent and/or part-time) where and when applicable to the sample type and through-put. o Perform o Continued competence in understanding and application of ISTA and ISO/IEC 17025 in test aspects. o