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Senior Director Regulatory Affairs, Surgery EMEA G5

Job in 6300, Zug, Kanton Zug, Switzerland
Listing for: 8525-Cilag GmbH International Legal Entity
Full Time position
Listed on 2026-07-06
Job specializations:
  • Management
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 91903 - 119473 CHF Yearly CHF 91903.00 119473.00 YEAR
Job Description & How to Apply Below

Johnson & Johnson Med Tech is 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.

Key Responsibilities
  • Lead teams responsible for execution of regulatory activities, ensuring compliance with internal Johnson & Johnson policies and external regulatory requirements across Med Tech 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.
  • Own and oversee complex regulatory projects impacting regional operations and compliance.
  • Represent J&J Med Tech 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 Med Tech 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.
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Position Requirements
10+ Years work experience
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