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- Tasks: Lead global healthcare regulatory strategy and engage with senior stakeholders.
- Company: Join GS1, a trusted partner in healthcare regulation and standards.
- Benefits: Competitive salary, global travel opportunities, and professional development.
- Why this job: Shape the future of healthcare through innovative regulatory frameworks.
- Qualifications: 10+ years in healthcare regulation with strong stakeholder engagement skills.
- Other info: Dynamic role with a focus on digital health and international standards.
The predicted salary is between 72000 - 108000 £ per year.
The Director, Healthcare Global Regulatory Affairs and Public Policy is a leadership role responsible for shaping and advancing GS1’s global healthcare regulatory and public policy agenda. The role operates at the intersection of healthcare regulation, international standards, and digital health, engaging at senior levels with regulators, governments, industry associations, and global institutions to support the adoption of harmonised, standards-based regulatory frameworks.
The role works in close alignment with GS1’s public policy strategy and plays a critical role in positioning GS1 as a trusted global partner in healthcare regulation, interoperability, identification, and traceability.
Role Purpose
The Director leads GS1’s global healthcare regulatory engagement to enable safer patient outcomes through improved data quality, interoperability, and traceability. The role anticipates and responds to regulatory and policy developments worldwide, translating them into strategic engagement, thought leadership, and practical adoption of GS1 standards across diverse regulatory environments. Operating in a complex, multicultural, and matrixed global context, the role delivers outcomes primarily through influence, credibility, and alignment rather than formal authority.
Key Responsibilities
- Lead the development and execution of GS1’s global healthcare regulatory and public policy strategy, aligned with GS1’s broader enterprise public policy priorities.
- Engage at senior levels with governments, international organisations, regulators, and authorities across medicines, MedTech, and digital health domains.
- Build and sustain strategic relationships with global and regional industry associations and healthcare stakeholders to support regulatory alignment and standards adoption.
- Provide recognised subject matter expertise and thought leadership through position papers, policy inputs, and strategic guidance supporting implementation of GS1 standards.
- Represent GS1 as a credible and neutral voice at international regulatory forums, conferences, and policy meetings.
- Lead and develop a global regulatory and regional engagement team, ensuring effective delivery against strategic objectives and capability building across regions.
- Collaborate closely with GS1 Member Organisations and internal teams to support education, regulatory alignment, and coordinated global engagement.
Future Focus
A key focus of the role is strengthening GS1’s positioning within the evolving digital health ecosystem. This includes supporting regulatory innovation, enabling digitised regulatory processes, and reinforcing the value of international standards in accelerating safe, interoperable, and efficient healthcare systems worldwide.
Education and Experience
- Minimum 10 years’ experience in pharmaceutical and/or MedTech regulatory environments, with demonstrated ability to engage effectively with healthcare authorities and regulators.
- Relevant industry experience within a healthcare manufacturer, supplier, wholesaler, or related organisation; practical experience with GS1 standards is a strong advantage.
- Proven success operating in complex, international, and multicultural environments.
- Demonstrated track record in roles requiring neutrality, credibility, and influence, where outcomes are achieved through alignment and persuasion.
- Experience in global health, digital health, or standards-related regulatory initiatives is highly desirable.
Skills and Competencies
- Deep understanding of pharmaceutical and MedTech regulatory frameworks and stakeholder expectations.
- Experience in leading teams, aligning for success, coaching and developing others. One direct report.
- Strong network of senior regulator connections across the Southern hemisphere.
- Working knowledge of regulatory environments in developing and transitional markets, including the Southern Hemisphere.
- Strong collaboration and stakeholder engagement skills within matrixed, global organisations.
- Excellent written and verbal communication skills in English, with the ability to engage diverse audiences at senior levels.
- High cultural intelligence, adaptability, and commitment to knowledge sharing and capability building across teams.
Additional Information
Up to 33% global travel may be required. GS1 is an Equal Opportunity Employer.
Director, Healthcare Global Regulatory Affairs and Public Policy in Wolverhampton employer: GS1
Contact Detail:
GS1 Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Director, Healthcare Global Regulatory Affairs and Public Policy in Wolverhampton
✨Tip Number 1
Network like a pro! Get out there and connect with industry professionals on LinkedIn or at conferences. The more people you know, the better your chances of landing that dream role.
✨Tip Number 2
Show off your expertise! Prepare to discuss your insights on healthcare regulations and public policy during interviews. We want to see how you can contribute to GS1’s mission and make an impact.
✨Tip Number 3
Practice your pitch! Be ready to articulate your vision for advancing GS1’s regulatory agenda. A clear and compelling narrative will help you stand out in interviews.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are genuinely interested in joining our team.
We think you need these skills to ace Director, Healthcare Global Regulatory Affairs and Public Policy in Wolverhampton
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter to highlight your experience in healthcare regulatory affairs. We want to see how your background aligns with the role, so don’t hold back on showcasing relevant achievements!
Showcase Your Expertise: This role is all about influence and credibility. Use your written application to demonstrate your subject matter expertise in regulatory frameworks and public policy. Share examples of how you've successfully engaged with stakeholders in the past.
Be Clear and Concise: We appreciate clarity! Keep your writing straightforward and to the point. Avoid jargon unless it’s industry-specific and relevant. Remember, we want to understand your qualifications without wading through unnecessary fluff.
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your materials and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team at GS1!
How to prepare for a job interview at GS1
✨Know Your Stuff
Make sure you have a solid understanding of GS1’s global healthcare regulatory framework and public policy agenda. Brush up on the latest trends in digital health and how they intersect with regulations. This will help you speak confidently about how your experience aligns with the role.
✨Build Your Network
Before the interview, try to connect with professionals in the industry, especially those who have worked with GS1 or similar organisations. Having insights from their experiences can give you an edge and show your proactive approach to networking.
✨Showcase Your Leadership Skills
Prepare examples that highlight your ability to lead teams and influence stakeholders without formal authority. Think of specific situations where you successfully navigated complex environments and achieved results through collaboration and persuasion.
✨Cultural Intelligence is Key
Given the multicultural nature of the role, be ready to discuss your experiences working in diverse teams and how you’ve adapted your communication style. Highlight any previous roles where you’ve had to engage with international regulators or stakeholders, showcasing your adaptability and cultural awareness.