Clinisys is seeking a Senior Regulatory Affairs Specialist to lead regulatory activities across global markets throughout the product lifecycle. You will collaborate with Quality, Clinical Safety, Product Management, R&D and Legal to shape regulatory strategy and submissions.
You will prepare filings, assess changes, and guide cross-functional teams through audits, registrations and market access. A strong background in medical devices or healthcare software is essential.
#J-18808-Ljbffr
Senior Regulatory Strategist – Global MedTech & SaMD | Remote employer: Clinisys
Clinisys is an exceptional employer that fosters a collaborative and innovative work culture, where employees are empowered to make a real impact in the healthcare sector. With a strong focus on professional development, you will have ample opportunities for growth while working alongside talented teams dedicated to optimising laboratory workflows and enhancing data quality through AI. Located in Woking, you'll enjoy a vibrant community and the chance to travel across the UK and Ireland, making your role both dynamic and rewarding.
