facilitation of change controls Assist on artwork and related projects Implement and manage a Pharmacoviligance that only quality products are released in to the market Ensure that the batch documents reviewed during per annum. Manage and record technical, quality related queries and customer returns with the relevant investigations and ensure that the QA/technical related matters are solved in a timely manner Implement the timely release of quality products in to the market Manage the relevant permits and complete the annual
facilitation of change controls Assist on artwork and related projects Implement and manage a Pharmacoviligance that only quality products are released in to the market Ensure that the batch documents reviewed during per annum. Manage and record technical, quality related queries and customer returns with the relevant investigations and ensure that the QA/technical related matters are solved in a timely manner Implement the timely release of quality products in to the market Manage the relevant permits and complete the annual
that only quality products are released into the market. Ensure that at least one executed batch record the timely release of quality products into the market. Ensure that retention and release samples are are kept of all product batches released to market. Quality Management Processes: Manage all final product investigations and ensure that all QA/technical related matters are solved in a timely manner. Ensure that etc. to all appropriate individuals (QA, RA, Marketing, Supply Chain, EXCO etc.). Support the Responsible
that only quality products are released into the market. Ensure that at least one executed batch record the timely release of quality products into the market. Ensure that retention and release samples are are kept of all product batches released to market. Quality Management Processes: Manage all final product investigations and ensure that all QA/technical related matters are solved in a timely manner. Ensure that etc. to all appropriate individuals (QA, RA, Marketing, Supply Chain, EXCO etc.). Support the Responsible
management of South Africa and some Southern African markets like Botswana and Namibia for an allocated part companies generic portfolio of products. Future markets and portfolios of products could be included as portfolio for South Africa and the Southern African markets. Requires close collaboration with the regulatory Offices, Labelling teams, Artwork centres, Cluster/Market, and any other key stakeholders to ensure the filing Regulatory Science/CMC, Submissions Management, Cluster/Markets, and other key stakeholders. Ensure and oversee
the RA Manager and cross functional team and marketing teams on the regulatory submission progress of with international priorities and local brand marketing strategy. On-going proactive identification and GRP standards in the following process areas: Marketing Authorization Applications License maintenance relevant to job profile. Marketing Authorization Applications: Submit Marketing Authorization Applications for accuracy. Review of registration status & market specific information for accuracy and completeness