At a Glance
- Tasks: Lead regulatory policy and compliance activities, ensuring alignment with global requirements.
- Company: Join a leading healthcare company committed to innovation and compliance.
- Benefits: Competitive salary, professional development, and a diverse work environment.
- Other info: Opportunities for career growth and international collaboration.
- Why this job: Make a real impact in regulatory affairs within a global organisation.
- Qualifications: Bachelor's degree in relevant field and 8-10 years of experience required.
The predicted salary is between 60000 - 80000 £ per year.
As Associate Director, Regulatory Policy, you will provide leadership and subject‑matter expertise in regulatory policy and compliance, supporting the development, interpretation, and implementation of global and regional regulatory requirements for DePuy Synthes.
Key Responsibilities
- Lead regulatory policy and compliance activities, ensuring alignment with applicable global, regional, and local regulatory requirements.
- Interpret evolving regulatory policies and guidance and assess impact on products, processes, and business strategies.
- Develop and maintain internal regulatory policies, standards, and guidance documents.
- Provide expert regulatory policy advice to cross‑functional stakeholders, including Regulatory Affairs, Quality, and business leaders.
- Support regulatory inspections, audits, and assessments related to policy and compliance topics.
- Monitor regulatory trends and emerging requirements, proactively identifying risks and opportunities.
- Partner with global and regional teams to drive consistent application of regulatory policies.
- Contribute to continuous improvement initiatives to strengthen regulatory compliance and governance frameworks.
Qualifications
- Bachelor’s degree in Regulatory Affairs, Life Sciences, Engineering, Law, or related discipline (required)
- Advanced degree or professional certification in Regulatory Affairs or Compliance (preferred)
Professional Experience and Skills
- Typically 8–10 years of progressive experience in regulatory affairs, regulatory policy, or compliance within a regulated industry (required)
- Strong understanding of global regulatory frameworks and policy development
- Experience interpreting regulations and translating requirements into practical guidance
- Proven ability to influence and advise senior stakeholders on regulatory policy matters
- Experience in medical devices, healthcare, or other highly regulated industries (preferred)
- Exposure to regulatory inspections, audits, or authority interactions (preferred)
- Experience working in a global or matrixed organization (preferred)
- Demonstrated success driving regulatory or compliance process improvements (preferred)
- Familiarity with US, EU MDR, China, and other major international regulatory frameworks (preferred)
- Effective written and verbal communication skills
- Strong analytical, problem‑solving, and documentation skills
Additional Requirements
- Language: English required; additional European languages preferred
- Travel: Limited; occasional international travel as needed
- Certifications: RAC or equivalent preferred but not required
Required Skills
- Analytical Reasoning
- Business Writing
- Compliance Risk
- Fact‑Based Decision Making
- Industry Analysis
- Legal Support
- Mentorship
- Organizing
- Product Licensing
- Public Policies
- Regulatory Affairs Management
- Regulatory Compliance
- Regulatory Development
- Regulatory Environment
- Risk Assessments
- Strategic Thinking
- Technical Credibility
Preferred Skills
- Analytical Reasoning
- Business Writing
- Compliance Risk
- Fact‑Based Decision Making
- Industry Analysis
- Legal Support
- Mentorship
- Organizing
- Product Licensing
- Public Policies
- Regulatory Affairs Management
- Regulatory Compliance
- Regulatory Development
- Regulatory Environment
- Risk Assessments
- Strategic Thinking
- Technical Credibility
Associate Director, Regulatory Policy employer: 6010-Biosense Webster Inc. Legal Entity
At DePuy Synthes, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the field of regulatory policy and compliance. Our employees benefit from comprehensive professional development opportunities, a commitment to diversity and inclusion, and the chance to make a meaningful impact in the healthcare industry. With locations in Zuchwil, Diegem, and the UK, we provide a supportive environment where your expertise can thrive and contribute to our mission of advancing healthcare solutions.
Contact Details:
6010-Biosense Webster Inc. Legal Entity Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director, Regulatory Policy
✨Tip Number 1
Network like a pro! Reach out to folks in your industry on LinkedIn or at events. A friendly chat can lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by researching the company and its regulatory policies. Show them you’re not just another candidate; you’re genuinely interested in their mission and how you can contribute.
✨Tip Number 3
Practice your answers to common interview questions, especially those related to regulatory compliance. We all know it’s about showcasing your expertise, so be ready to impress!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who take that extra step.
We think you need these skills to ace Associate Director, Regulatory Policy
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the Associate Director, Regulatory Policy role. Highlight your relevant experience in regulatory affairs and compliance, and show us how you can bring value to our team.
Showcase Your Expertise:We want to see your knowledge in action! Use specific examples from your past work to demonstrate your understanding of global regulatory frameworks and how you've successfully navigated them.
Be Clear and Concise:When writing your application, keep it straightforward. We appreciate clarity, so avoid jargon and get straight to the point about your skills and experiences that align with the job description.
Apply Through Our Website:Don’t forget to submit your application through our official website! It’s the best way for us to receive your details and ensures you’re considered for the role. We can’t wait to hear from you!
How to prepare for a job interview at 6010-Biosense Webster Inc. Legal Entity
✨Know Your Regulatory Frameworks
Make sure you brush up on the global regulatory frameworks relevant to the role, especially US and EU MDR. Being able to discuss how these regulations impact product development and compliance will show your expertise and readiness for the position.
✨Prepare for Scenario-Based Questions
Expect questions that ask you to interpret regulatory policies or assess their impact on business strategies. Practise articulating your thought process and decision-making skills in these scenarios, as this will demonstrate your analytical reasoning and problem-solving abilities.
✨Showcase Your Leadership Skills
As an Associate Director, you'll need to lead cross-functional teams. Be ready to share examples of how you've influenced senior stakeholders or driven compliance initiatives in the past. This will highlight your ability to mentor and guide others in a regulatory context.
✨Stay Updated on Regulatory Trends
Research current trends and emerging requirements in regulatory affairs. Being able to discuss recent changes or challenges in the industry will not only show your passion for the field but also your proactive approach to identifying risks and opportunities.
