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Job Function:

Regulatory Affairs Group

Job Sub Function:

Regulatory Affairs

Job Category:

People Leader

All Job Posting Locations:

Zug, Switzerland

Job Description:

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

• Bachelor’s degree required
• 10–12 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., Master’s)
• Background in Science, Engineering, or related field
• Experience in Medical Devices industry
• Global or multi-region experience

 

 

Required Skills:

 

 

Preferred Skills:

Business Writing, Compliance Risk, Cross-Functional Work, Developing Others, Fact-Based Decision Making, Inclusive Leadership, Industry Analysis, Innovation, Leadership, Legal Support, Operations Management, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Risk Management, Strategic Thinking