Senior Quality Assurance Manager
We are exclusively partnered with an exciting CDMO that are investing heavily to expand their offering across drug development, with a real focus on biologics and wider biopharmaceuticals.
As part of this expansion, this position is a brand new senior Quality function that must be willing and able to take on all aspects of quality assurance responsibilities in relation to biologics drug development.
Taking ownership of developing and implementing a quality management system, the successful candidate will take technical responsibility for key regulations specific to GMP, biologics and CMC technical transfer documentation.
Outstanding stakeholder management skills are essential given the need to liaise cross functionally internally, as well as directly with clients.
For further details, please contact Mark Bux-Ryan.
Key experience:
Quality, assurance, QA, biologics, biopharmaceutical, CFR, 21, 210, 211, 600, 610, GMP, manufacturing, development, CMC, technical, transfer, management, system, CAPA, deviation, change, control
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