At a Glance
- Tasks: Lead global regulatory and environmental compliance programs for logistics operations.
- Company: Join a leading medical device company committed to innovation and sustainability.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Collaborative culture with a focus on continuous improvement and career advancement.
- Why this job: Make a real impact on global compliance and sustainability in a dynamic environment.
- Qualifications: 8+ years in Regulatory Affairs or Environmental Compliance; strong project management skills.
The predicted salary is between 60000 - 80000 £ per year.
The Program Manager, Product Environmental Compliance & Regulatory Affairs (PEC & RA) Global Logistics Operations (GLO) is responsible for planning, coordinating, and executing global Regulatory Affairs and Product Environmental Compliance programs applicable to Global Logistics activities and distribution networks. This role ensures that GLO Operations—including EU and global distribution centers—are compliant with applicable regulatory requirements related to environmental product compliance, packaging, batteries, and Economic Operator obligations. The Program Manager acts as the primary interface between GLO, Corporate RA/PEC programs, and cross‑functional stakeholders to ensure timely, consistent, and compliant implementation of regulatory requirements.
Key Activities & Responsibilities
- Leading global RA & PEC programs applicable to Global Logistics, ensuring alignment with Corporate and Divisional regulatory strategies and timelines.
- Establishing and maintaining program governance, including scope definition, milestones, risk management, dependency tracking, and executive reporting.
- Coordinating implementation of Product Environmental Compliance (PEC) requirements impacting logistics and distribution activities, including packaging, batteries, and restricted substances.
- Act as the official correspondent or responsible person to relevant health authorities for GLO sites.
- Evaluating impact of changing global regulations, including PEC requirements, on the GLO network and communicating impact to leadership.
- Supporting compliance with applicable regulations such as Packaging and Packaging Waste Regulation (EU) 2025/40 (PPWR), Battery Regulation (EU) 2023/1542 (BWBR), and related implementing acts.
- Report on budget actuals and project costs to management for activities supporting regulatory requirements.
- Training staff on, executing and monitoring registration and listing obligations for GLO sites globally.
- Supporting health authority and notified body audits as required and responding to health authority queries.
- Collaborating with Regulatory Affairs function to identify, draft and communicate device shortages to relevant health authorities.
- Coordinating RA‑related Economic Operator obligations (Importer and Distributor) as they apply to GLO operations, in close collaboration with Corporate RA and Legal.
- Acting as the primary GLO liaison to Corporate PEC and RA programs to ensure consistent interpretation, deployment, and execution across regions.
- Partnering with Quality Assurance, Supply Chain, Packaging Engineering, Sustainability, Operations, and Business stakeholders to drive end‑to‑end regulatory readiness.
- Ensuring appropriate regulatory documentation, evidence, and records are maintained to support audits, inspections, and market access requirements.
- Monitoring program performance through defined KPIs and readiness indicators, identifying gaps and driving timely corrective actions.
- Supporting continuous improvement of regulatory and compliance processes within Global Logistics.
- Promoting awareness of regulatory and environmental compliance requirements throughout the GLO organization.
Education
- Hon. Bachelor’s degree in Science, Engineering or related subject or equivalency is mandatory.
- Masters degree in Science, Engineering or related subject is preferred.
- Regulatory Affairs Certification (RAC) in medical devices is preferred.
Experience
- 8+ years of experience in Regulatory Affairs, Product Environmental Compliance, or regulatory program management within a regulated industry (medical devices preferred).
- Demonstrated experience managing complex, cross‑functional, global programs.
- Working knowledge of EU environmental, packaging, and battery regulations and their impact on logistics and distribution activities.
- Experience working within ISO 13485 / MDR / FDA‑regulated quality systems.
- Experience supporting distribution, logistics, or supply chain activities is preferred.
Travel Percentage: 20%
Stryker is an equal opportunity employer.
Global Regulatory & Environmental Compliance Program Lead in Newbury employer: Stryker
Stryker is an exceptional employer that prioritises employee growth and development, offering a dynamic work culture where innovation and collaboration thrive. As the Global Regulatory & Environmental Compliance Program Lead, you will be at the forefront of ensuring compliance within our global logistics operations, while enjoying comprehensive benefits and opportunities for professional advancement in a supportive environment. Located in a vibrant area, Stryker fosters a commitment to sustainability and regulatory excellence, making it a rewarding place to build your career.
StudySmarter Expert Advice🤫
We think this is how you could land Global Regulatory & Environmental Compliance Program Lead in Newbury
✨Tip Number 1
Network like a pro! Reach out to folks in the industry on LinkedIn or at events. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and its regulatory practices. We want to see you shine, so practice answering common questions and think about how your experience aligns with their needs.
✨Tip Number 3
Showcase your expertise! Bring examples of your past work in regulatory affairs and compliance to the table. We love seeing how you’ve tackled challenges and driven results in previous roles.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we’re always looking for passionate individuals who are ready to make an impact in global logistics.
We think you need these skills to ace Global Regulatory & Environmental Compliance Program Lead in Newbury
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the role of Global Regulatory & Environmental Compliance Program Lead. Highlight your experience in regulatory affairs and environmental compliance, especially in logistics. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Share specific examples of your past experiences that relate to the key activities and responsibilities mentioned in the job description. Let us know why you’re excited about joining StudySmarter!
Showcase Your Skills:Don’t forget to showcase your skills relevant to the position, like project management and cross-functional collaboration. We love seeing candidates who can demonstrate their ability to lead global programs and manage complex regulatory requirements. Make it clear how you can contribute to our team!
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and ensure it gets the attention it deserves. Plus, you’ll find all the details you need about the role there!
How to prepare for a job interview at Stryker
✨Know Your Regulations
Make sure you brush up on the latest EU environmental regulations, especially those related to packaging and batteries. Being able to discuss how these regulations impact logistics will show that you're not just familiar with the role but also proactive about compliance.
✨Showcase Your Experience
Prepare specific examples from your past roles where you've successfully managed complex regulatory programs. Highlight your experience in cross-functional collaboration and how you’ve navigated challenges in a regulated industry—this will demonstrate your capability to lead in this position.
✨Understand the Company’s Goals
Research Stryker's mission and values, particularly in relation to sustainability and compliance. Be ready to discuss how your personal values align with theirs and how you can contribute to their goals in global logistics operations.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's current regulatory challenges or upcoming projects. This shows your genuine interest in the role and helps you gauge if the company culture aligns with your expectations.
