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Site Quality Assurance Manager
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- Key processes that the QA Manager has ownership of includes executed batch record review, validation master plans (VMP) and deviation/event/CAPA.
- Provision of QA oversight and support for Operations in the following key area/activities: manufacturing across all phases of development and commercial manufacture, packaging and materials management on site.
- The VMP must be established and kept up to date by the local site owner of the operation (e.g. head of manufacturing/technical services) and the responsible Quality Operations, Quality Systems and Quality Control managers Co-ordinate QA functions for assigned areas of responsibility and provide for QA Operations liaisons with functional departments in Production, Quality and Commercial.
- Responsible for leading Manufacturing/Event Investigations and Corrective and Preventative Action (CAPA) Triage meetings, where necessary.
- Minimum of 8 years progressive experience in the quality control, quality assurance, manufacturing function, or release roles supporting commercial registered product operations for animal health or human health products.
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