At a Glance
- Tasks: Lead global compliance programs ensuring environmental regulations are met in logistics.
- Company: Join a leading medical device company committed to sustainability and innovation.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Dynamic role with a chance to collaborate across various departments and drive change.
- Why this job: Make a real difference in environmental compliance while working on impactful global projects.
- Qualifications: 8+ years in regulatory affairs with a focus on environmental compliance preferred.
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.
Program Manager, Product Environmental Compliance & Regulatory Affairs 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 a Program Manager in Product Environmental Compliance & Regulatory Affairs, you will be at the forefront of ensuring compliance within global logistics operations, while benefiting from comprehensive training and support in a company committed to sustainability and regulatory excellence. With a focus on meaningful work and a commitment to diversity and inclusion, Stryker provides a rewarding environment for professionals looking to make a significant impact in their field.
StudySmarter Expert Advice🤫
We think this is how you could land Program Manager, Product Environmental Compliance & Regulatory Affairs in Newbury
✨Tip Number 1
Network like a pro! Reach out to folks in the industry, attend relevant events, and connect with people on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its regulatory landscape. Understand their compliance challenges and be ready to discuss how your experience aligns with their needs. Show them you’re not just another candidate!
✨Tip Number 3
Practice your pitch! Be clear about your experience in Regulatory Affairs and Product Environmental Compliance. Highlight specific projects where you’ve led cross-functional teams or navigated complex regulations—this will set you apart.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who are proactive and engaged with our brand.
We think you need these skills to ace Program Manager, Product Environmental Compliance & Regulatory Affairs in Newbury
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the Program Manager role. Highlight your experience in Regulatory Affairs and Product Environmental Compliance, and show us how your skills align with our needs at StudySmarter.
Showcase Relevant Experience:We want to see your 8+ years of experience shining through! Be specific about your past roles in managing complex, cross-functional programmes, especially in regulated industries like medical devices. This will help us understand your fit for the position.
Be Clear and Concise:When writing your application, keep it straightforward. Use clear language and bullet points where possible to make it easy for us to read. We appreciate a well-structured application that gets straight to the point!
Apply Through Our Website:Don’t forget to submit your application through our 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 see what you bring to the table!
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 Project Management Skills
Prepare examples of complex, cross-functional projects you've managed in the past. Highlight your experience with program governance, risk management, and how you’ve successfully met milestones. This will demonstrate your capability to lead global RA & PEC programs effectively.
✨Understand the Company’s Goals
Research Stryker's mission and values, particularly in relation to sustainability and regulatory compliance. Be ready to discuss how your personal values align with theirs and how you can contribute to their goals in Global Logistics Operations.
✨Prepare for Scenario Questions
Think about potential scenarios you might face in this role, such as handling a sudden change in regulations or managing a compliance audit. Practising your responses will help you articulate your problem-solving skills and readiness for challenges in the role.
