Senior Director, Regulatory Affairs – EMEA/Canada (EP/NV)

About the role

Johnson & Johnson MedTech is seeking a Senior Director of Regulatory Affairs to lead the EMEA and Canada region for its Electrophysiology (EP) and Neurovascular (NV) businesses. Based in Ireland, Switzerland, or Israel, you will shape regulatory strategy, guide product approvals, and ensure ongoing compliance across diverse markets.

Key responsibilities

• Lead regional Regulatory Affairs teams to accelerate product approvals and support business growth.
• Develop and execute regional regulatory strategies that reflect country‑specific dynamics and global business objectives.
• Represent the regional RA function in global leadership forums, providing market insights and driving strategic priorities.
• Monitor regulatory changes, assess impact, and direct appropriate regional actions to maintain product compliance.
• Build a diverse, capable regulatory workforce through recruitment, retention, and development initiatives.
• Represent Johnson & Johnson MedTech in external regulatory forums and industry discussions.

Required profile

• Extensive experience in regulatory affairs for medical devices, preferably within EP and NV product lines.
• Proven leadership of regional or global regulatory teams.
• Strong strategic thinking and ability to influence senior business leaders.
• Excellent judgment and decision‑making skills in complex, multi‑market environments.
• Commitment to fostering an inclusive and culturally aware workforce.

Required skills

What we offer

• Opportunity to lead regulatory strategy for innovative medical technologies.
• Collaborative, inclusive work environment aligned with Johnson & Johnson’s Credo.
• Global exposure across EMEA and Canada markets.