Senior Director Regulatory Affairs, Surgery EMEA G5 (m/f/d)

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.
  

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

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