Regulatory Affairs Job at Bioventus, UK | Life Sciences | Apply Now
Are you ready to work for a more active world? If you are looking for a dynamic Regulatory Affairs Job where your work directly impacts patient mobility and wellness, Bioventus is hiring. This remote Job in UK offers a unique opportunity to join a market leader in pain treatment and joint preservation. For professionals seeking a highly impactful Life Sciences Job, this role places you at the forefront of global medical device compliance.
- Job Position: Regulatory Project Specialist
- Location: Remote, UK
- Job requisition ID: R-2026-05-001641
About The Company
Bioventus is a global market leader dedicated to developing clinically proven and cost-effective solutions for joint preservation, restorative therapies, and bone graft substitutes. Working here means taking on a Life Sciences Job that truly matters—the company generates over $500 million in annual revenue and helps more than 700,000 people every year regain their active lifestyles. By stepping into this Regulatory Affairs Job, you will join a diverse team of over 1,100 global colleagues who put patient needs at the forefront of every choice they make.
Regulatory Affairs Job – Key Responsibilities
As a Regulatory Project Specialist, you will ensure the timely and effective communication of regulatory approvals, renewals, and legalizations. This Job in UK is highly cross-functional, requiring you to support internal international teams while navigating complex government agency requirements.
- Global Submissions: Support various documentation applications to secure new product approvals and renew licenses, ensuring existing registrations are maintained globally.
- Database Management: Maintain accurate records of regulatory submissions and approvals, specifically utilizing the EUDAMED (European Database on Medical Devices) system.
- Official Certifications: Manage and process high-priority requests for Certificates to Foreign Government (CFGs), Certificates of Manufacture and Free Sale, and Certificates of Exportability.
- Administrative Coordination: Coordinate the legal legalization of regulatory documents and manage administrative payments to international government agencies.
- Compliance & Ethics: Uphold the Bioventus Code of Compliance and Ethics, acting as a crucial regulatory gatekeeper and resolving inquiries from regulatory agencies.
Candidate Profile For Regulatory Affairs Job
To succeed in this Life Sciences Job, you need a blend of meticulous organizational skills and specific medical device industry knowledge.
- Educational Foundation: A Bachelor’s Degree in Life Sciences, Engineering, or a closely related discipline is required.
- Targeted Experience: 1 to 2 years of proven experience in a Regulatory Affairs Job, preferably within the medical device industry.
- Technical Knowledge: Hands-on experience with the European Database on Medical Devices (EUDAMED) is a significant advantage.
- Communication Skills: Clear, concise, and timely oral and written communication skills to effectively partner with cross-functional teams and international agencies.
- Operational Pacing: The ability to thrive in a fast-paced, data-driven environment while setting firm priorities and maintaining strict project schedules.
In summary, the Regulatory Project Specialist role at Bioventus is a standout Life Sciences Job for early-career professionals ready to make a tangible global impact. By securing this remote Job in UK, you will play a critical role in bringing innovative, safety-recognized medical devices to patients worldwide. If you have the required medical device background and the drive to excel in a fast-paced Regulatory Affairs Job, apply today to advance your career with an industry leader.
