Teva Pharmaceuticals is looking for an Associate Director, Global Quality Compliance Lead in Crynant, UK. The role involves supporting global pharmaceutical manufacturing operations and ensuring compliance with cGMP and regulatory standards.
The successful candidate will lead quality initiatives, inspection readiness activities, and investigations, focusing on sterility assurance and patient safety. A Bachelor's degree and 8-12 years of relevant experience in pharmaceutical quality/compliance are essential.
Candidates must be prepared for up to 30% travel.
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