Johnson & Johnson Innovative Medicine is seeking a Manager, EU Medical Devices & IVDR Regulation to serve as the SME for EU Medical Device and In Vitro Diagnostic Regulations.
Based in Beerse, Belgium; Allschwil, Switzerland; or Maidenhead, UK, you will influence regulatory compliance strategies within the Clinical Quality Management System and partner across Regulatory Affairs, Quality, Clinical Development and more.
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EU MDR/IVDR Regulation Manager - Med Devices & IVD in High Wycombe employer: Johnson & Johnson Innovative Medicine
At Johnson & Johnson Innovative Medicine, we pride ourselves on fostering a collaborative and inclusive work culture that empowers our employees to thrive. As a Regulatory Medical Writer II, you will benefit from our commitment to professional development, with ample opportunities for growth and learning in a dynamic environment. Located in the UK, our hybrid work model offers flexibility while allowing you to contribute to impactful projects that advance healthcare globally.
Contact Details:
Johnson & Johnson Innovative Medicine Recruitment Team
