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Responsible to supervise and lead the Laboratory release function including Raw Materials, Intermediates, DPI and API’s (including the stability program) and In Process Control and provide core technical support in areas of chromatography,
Responsible for developing and overseeing a robust Quality Assurance strategy focused on the transfer of New Product Introduction (NPI) QC methods to manufacturing sites and Third-Party Laboratories. This role supports the Test Method Gate Review process,
Responsible for all tasks and resources including cross functional co-ordination required to complete relevant QC microbiology activities within regulated environment in the required timeframe. Management of QC Microbiology team to carry out tasks.