Regulatory Affairs Specialist
2 days ago
Life. Unlimited. At Smith+Naphew we design and manufacture technology that takes the limits off living. Are you passionate about making a real impact in healthcare? Join us as a Regulatory Affairs Specialist and play a key role in ensuring our advanced wound care products meet global standards. This is your chance to influence innovation and help deliver life‑changing solutions to patients worldwide. What will you be doing? Managing project and regulatory involvement with direct management supervision. This includes providing on‑going regulatory advice to project teams throughout the product and process development to ensure regulatory concerns are planned and accounted for and the relevant data generated to meet project objectives. To compile and review, as required, regulatory submissions in accordance with national requirements to ensure appropriateness and consistency in content and presentation of information both within and between registration applications. This can include European Technical Files, US 510(k) applications and device listings as required. To complete the requirements of the Smith & Nephew regulatory submission plan per the requirements of RIMSYS (recording/tracking of regulatory submission application). To review and approve artwork, labelling and promotional literature and advise on its acceptability/compliance with regulations and registered details. To review and approve change control impact assessments for products. What will you need to be successful? Success in this role means being proactive, detail‑oriented, and collaborative. You’ll need: A background in life sciences or similar discipline Experience with medical device regulations and submissions Strong organisational skills and proficiency in MS applications The ability to build effective relationships across teams and with external stakeholders You. Unlimited. We believe in creating the greatest good for society. Our strongest investments are in our people and patients we serve. Inclusion and Belonging: Committed to welcoming, celebrating and thriving on inclusion and belonging. Learn more about our Employee Inclusion Groups on our website (www.smith-nephew.com) Your Future: Generous annual bonus and pension schemes, Save As You Earn share options. Work/Life Balance: Flexible vacation and time off, paid holidays and paid volunteering hours, so we can give back to our communities Your Wellbeing: Private health and dental plans, healthcare cash plans, income protection, life assurance and much more. Flexibility: Hybrid working model (for most professional roles). Training: Hands‑on, team‑customised, mentorship. Extra Perks: Discounts on gyms and fitness clubs, salary sacrifice bicycle and car schemes and many other employee discounts. Stay connected by joining our Talent Community. We're more than just a company - we're a community Follow us on LinkedIn to see how we support and empower our employees and patients every day. Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek into You. Unlimited., life, culture, and benefits at S+N. Explore our website and learn more about our mission, our team, and the opportunities we offer. #J-18808-Ljbffr
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York and North Yorkshire, United Kingdom Smith & Nephew Full timeA global healthcare company is looking for a Regulatory Affairs Specialist in York, England, to oversee regulatory submissions and ensure compliance with medical device regulations. The ideal candidate will have a background in life sciences, experience with medical device regulations, and a proactive approach to collaboration across teams. This role comes...
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Regulatory Affairs Specialist
2 days ago
Hull and East Yorkshire, United Kingdom Smith+Nephew Full timeRegulatory Affairs Specialist – Smith+ Nephew Life. Unlimited. At Smith+ Nephew we design and manufacture technology that takes the limits off living. Are you passionate about making a real impact in healthcare? Join us as a Regulatory Affairs Specialist and play a key role in ensuring our advanced wound care products meet global standards. This is your...
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Regulatory Affairs Specialist
4 days ago
Hull and East Yorkshire, United Kingdom Smith & Nephew Full timeRegulatory Affairs Specialist page is loaded## Regulatory Affairs Specialistlocations: UK - Hull GBU Officetime type: Full timeposted on: Posted Todayjob requisition id: R86922**Life. Unlimited.** At Smith+Nephew we design and manufacture technology that takes the limits off living.You’ll be at the heart of our regulatory strategy, guiding projects...
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Regulatory Affairs Specialist
2 days ago
Hull and East Yorkshire, United Kingdom Smith+Nephew Full timeA leading global healthcare company is seeking a Regulatory Affairs Specialist in Hull and East Yorkshire. The role involves managing regulatory submissions and providing key advice to project teams ensuring that advanced wound care products meet global standards. A background in life sciences, experience in medical device regulations, and strong...
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Hull and East Yorkshire, United Kingdom Smith & Nephew Full timeA global medical technology company is seeking a Regulatory Affairs Specialist to oversee project compliance from concept to market. This role requires a background in life sciences, experience with medical device regulations, and strong organisational skills. Successful candidates will thrive in a collaborative environment and build relationships with...
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Regulatory Affairs and Compliance Manager
5 days ago
Yorkshire and Humberside, United Kingdom Page Group Full timeRegulatory Affairs and Compliance Manager **Client Details** Utilities Business **Description** I am recruiting an 18-month contract for a Regulatory Affairs & Compliance Manager with a utilities business in Yorkshire (hybrid working). You will: - Managing the PR24 Assurance and Compliance workstream in the PR24 Programme ensuring assurance of all...
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Regulatory Affairs Specialist
3 days ago
Hull, East Yorkshire, United Kingdom Smith+Nephew Full timeLife. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. Are you passionate about making a real impact in healthcare? Join us as a Regulatory Affairs Specialist and play a key role in ensuring our advanced wound care products meet global standards. This is your chance to influence innovation and help deliver...
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Regulatory Affairs Manager
1 week ago
Cambridgeshire and Peterborough, United Kingdom Walker Cole International Full timeRegulatory Affairs Manager A leading medical device and IVD manufacturer based in Cambridgeshire is looking for a Regulatory Affairs Manager. This company develops and supplies innovative diagnostic solutions used worldwide. As a Regulatory Affairs Manager, you’ll play a key role in ensuring products meet global regulatory, safety, and quality standards...
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Regulatory Affairs Officer
2 weeks ago
Puddington, Cheshire West and Chester, United Kingdom Nexus Life Sciences Full timeRegulatory Affairs Officer – Pharmaceuticals Salary: £40,000 – £50,000 DOE. Are you a detail-oriented Regulatory Affairs professional with a passion for ensuring pharmaceutical compliance across global markets? This is an excellent opportunity for an RA officer to join a well-established pharmaceutical manufacturer with a strong reputation for...
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Regulatory Affairs Manager
2 weeks ago
Cambridgeshire and Peterborough, United Kingdom Russell Taylor Group Ltd Full timeRegulatory Affairs Manager Location: Cambridgeshire Employment Type: (Full-time: Mon-Fri) (Hybrid: 2 - 3 days on site) We are seeking an experienced Regulatory Affairs Manager to lead global regulatory activities across a product portfolio and ensure the products remain safe, effective, and compliant for worldwide markets. This is an exciting opportunity for...
