Senior Director Regulatory Affairs, Surgery EMEA G5

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at .

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

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Johnson & Johnson MedTech are seeking a Senior Director Regulatory Affairs Surgery EMEA G5 (Mid-Size Markets) based in Switzerland.

The Senior Director Regulatory Affairs (RA) for G5 & Mid-size markets in EMEA Surgery serves as the regulatory leader overseeing all aspects of regulatory activities in these markets. This role contributes to the development and execution of regulatory strategies partners closely with senior business leaders and exercises independent judgment to drive business outcomes.

Key Responsibilities

• Lead teams responsible for execution of regulatory activities ensuring compliance with internal Johnson & Johnson policies and external regulatory requirements across MedTech Surgery.
• Develop and implement regulatory strategies aligned to evolving regulatory environments and business priorities.
• Build and lead high-performing teams focusing on talent development succession planning and capability building.
• Sponsor and oversee complex regulatory projects impacting regional operations and compliance.
• Represent J&J MedTech in external regulatory forums trade associations and interactions with regulatory authorities.
• Ensure adherence to global policies and regional regulatory requirements.
• Provide strategic regulatory guidance and advice to senior leadership.
• Support cross-functional initiatives and contribute to global/regional governance activities.

Required Qualifications

• Bachelors degree required
• 1012 years of relevant experience
• Strong regulatory affairs expertise within MedTech or related industry
• Proven leadership and people management capability
• Advanced communication and influencing skills
• Ability to make independent decisions impacting business outcomes

Preferred Qualifications

• Advanced degree (e.g. Masters)
• Background in Science Engineering or related field
• Experience in Medical Devices industry
• Global or multi-region experience

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