Teva in the United Kingdom is seeking a Senior Quality Manager, Device R&D to lead quality compliance across local and global R&D teams for combination products from concept through industrialization. You will review design specifications, risk management, verification/validation plans, and change controls to ensure regulatory alignment.
The role requires a degree in science or engineering (MSc/PhD preferred), strong GMP experience, ISO 13485 and CFR knowledge, and proven auditing and leadership
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Senior Quality Leader, Device R&D — GMP/ISO 13485 in Runcorn employer: Tevapharm
Teva Pharmaceuticals is an exceptional employer that fosters a collaborative and innovative work culture, where employees are encouraged to grow and develop their skills in the dynamic field of pharmaceuticals. With a strong commitment to employee well-being, Teva offers comprehensive benefits and opportunities for professional advancement, making it an ideal place for those looking to make a meaningful impact in quality control within a state-of-the-art lab environment.
