Regulatory Affairs Specialist
2 days ago
Ready to lead global regulatory strategy? Want to shape compliance for innovative medical technologies? Looking for flexibility, ownership, and international impact? A forward-thinking medical device company is seeking a Regulatory Affairs Manager to join its Quality and Compliance function, playing a pivotal role in managing global regulatory approvals across both established and emerging markets. This is an exciting opportunity to take ownership of international regulatory submissions, collaborate with cross-functional teams, and influence strategic direction — all within a business delivering life-enhancing technologies. Why This Role is Great As Regulatory Affairs Manager, you'll enjoy: Leading regulatory submissions and renewals across the UK, EU, US, and international markets. Acting as a key liaison with regulatory bodies, notified bodies, and in-country representatives. Supporting the creation and review of technical documentation that meets evolving global standards. Contributing to post-market surveillance, audits, and strategic compliance initiatives. Helping shape future market access plans in partnership with commercial and product teams. This role offers a mix of autonomy, influence, and hands-on technical engagement — ideal for someone looking to step into a strategic role without losing touch with the detail. About You This opportunity is perfect for someone who wants to work with a range of innovative technologies — from electromechanical devices to integrated software systems — and play a lead role in global regulatory operations. You’ll likely bring: Vast Experience in regulatory affairs or compliance within a medical device environment. A solid grasp of EU MDR (and legacy MDD), FDA requirements, and international submission processes. Experience managing Class IIa submissions and contributing to Technical Files. Confidence working across both medical and non-medical regulatory frameworks (e.g. low voltage, EMC). Excellent communication, document management, and cross-functional collaboration skills.
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Regulatory Affairs Specialist
6 days ago
Oxfordshire, United Kingdom Humand Talent Full timeReady to lead global regulatory strategy?Want to shape compliance for innovative medical technologies?Looking for flexibility, ownership, and international impact?A forward-thinking medical device company is seeking a Regulatory Affairs Manager to join its Quality and Compliance function, playing a pivotal role in managing global regulatory approvals across...
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Regulatory Affairs Specialist
7 days ago
Oxfordshire, United Kingdom Humand Talent Full timeReady to lead global regulatory strategy?Want to shape compliance for innovative medical technologies?Looking for flexibility, ownership, and international impact?A forward-thinking medical device company is seeking a Regulatory Affairs Manager to join its Quality and Compliance function, playing a pivotal role in managing global regulatory approvals across...
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Regulatory Affairs Specialist
7 days ago
Oxfordshire, United Kingdom Humand Talent Full timeReady to lead global regulatory strategy? Want to shape compliance for innovative medical technologies? Looking for flexibility, ownership, and international impact? A forward-thinking medical device company is seeking a Regulatory Affairs Manager to join its Quality and Compliance function, playing a pivotal role in managing global regulatory approvals...
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Regulatory Affairs Specialist
7 days ago
Oxford, Oxfordshire, United Kingdom Humand Talent Full timeReady to lead global regulatory strategy? Want to shape compliance for innovative medical technologies? Looking for flexibility, ownership, and international impact? A forward-thinking medical device company is seeking a Regulatory Affairs Manager to join its Quality and Compliance function, playing a pivotal role in managing global regulatory approvals...
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Oxford, Oxfordshire, United Kingdom ProPharma Full timeCompany profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world's largest RCO (Research Consulting Organization),...
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Regulatory Affairs Manager
7 days ago
Oxford, Oxfordshire, United Kingdom Barrington James Full timeLooking for a med dev/ post-market surveillance specialist looking for a step up Leadership opportunity Hybrid - Berkshire, Cambridge, Oxford area
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Regulatory Affairs Manager
7 days ago
Oxford, Oxfordshire, United Kingdom Barrington James Full timeLooking for a med dev/ post-market surveillance specialist looking for a step up Leadership opportunity Hybrid - Berkshire, Cambridge, Oxford area
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Business Compliance Associate
7 days ago
Oxfordshire, United Kingdom Humand Talent Full timeReady to lead global regulatory strategy? Want to shape compliance for innovative medical technologies? A forward-thinking medical device company is seeking a Regulatory Affairs Manager to join its Quality and Compliance function, playing a pivotal role in managing global regulatory approvals across both established and emerging markets. This is an...
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Clinical Supply Chain Manager
3 weeks ago
Oxford, Oxfordshire, United Kingdom Planet Pharma Full timeClinical Supply Manager Location: United Kingdom (Hybrid) Contract Type: 6-month contract with the potential to extend Global Pharmaceutical Organisation We're looking for a Clinical Supply Manager with a strategic mindset and strong operational focus to manage end-to-end clinical supply activities across global Phase I–IV studies. You'll play a...
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Quality, Compliance
2 weeks ago
Chilton, Oxfordshire, United Kingdom WIKA Instruments Ltd Full timeQuality, Compliance & Facilities Specialist Company Overview: For over 75 years, WIKA has been a renowned partner and competent specialist for any task in the field of measurement technology. With steadily growing efficiency, innovative technologies are applied when developing new products and system solutions. The reliability of the products and the...
