Senior Regulatory Strategist – Global MedTech & SaMD | Remote

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.

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