KeyMed (Medical & Industrial Equipment) Ltd. (OKM) is seeking a Process Validation Engineer to lead process validation activities in a manufacturing environment.
You will develop the Site Master Validation Plan, create risk-based protocols, and execute validation tasks while supporting other engineers and mentoring colleagues. The role requires understanding of FDA 21 CFR Part 820, ISO 13485:2016, and DOE-based validation methods.
#J-18808-Ljbffr
Process Validation Engineer - Hybrid Role in Medical Devices employer: OLYMPUS EUROPA SE & CO. KG
KeyMed (Medical & Industrial Equipment) Ltd. is an exceptional employer, offering a dynamic work environment in the heart of West Sussex, Hampshire, Berkshire, Cheltenham, and Gloucestershire. With a strong focus on patient care and employee well-being, we provide comprehensive benefits including private medical cover, a generous pension scheme, and wellness programmes, all while fostering a culture of integrity, innovation, and empathy. Our commitment to diversity and inclusion ensures that every team member feels valued and empowered to grow within their role.
Contact Details:
OLYMPUS EUROPA SE & CO. KG Recruitment Team
