Experienced leader needed to spearhead EU MDR compliance and regulatory strategy.

Responsibilities:

• Lead EU MDR compliance efforts, including transition plan and on-time product approvals.
• Manage high-performing regulatory team and oversee EU submissions.
• Possess deep understanding of EU MDR regulations and best practices.

Qualifications:

• Minimum 10 years of medical device regulatory affairs (EU focus).
• Proven leadership in MDD to MDR transition.
• Strong EU MDR expertise and excellent communication skills (English).