Senior Regulatory Affairs

A unique opportunity to take a key role on the leadership team of a highly successful and award-winning developer of naturally sourced, sustainable ingredients for regulated consumer products. They are the leader in their field, the market is exploding, this position will be paramount to this regulatory centric business’ continued global growth.The company...

**About us** For over 30 years, Surgical Innovations have proudly designed, developed and manufactured high quality, precision engineered instruments for mínimally invasive surgery and are a leading UK manufacturer of medical devices in its respective field. Our success is our people and we currently employ over 100 staff from our head office in Leeds. We...

Regulatory Affairs Specialist Location: Any Brenntag office within UK / Ireland (Hybrid - 2 days working from home) Contract Type: Full-time, Permanent Brenntag UK & Ireland is part of the global Brenntag Group, the world’s leading distributor of chemicals and ingredients. Headquartered in Leeds, we operate across 21 strategic sites in the UK and...

Johnson & Johnson MedTech is currently seeking a Senior Regulatory Affairs Associate. Location: Leeds Office, (hybrid model, 3 days in office 2 at home) At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are...

Regulatory Affairs Specialist Location: Any Brenntag office within UK / Ireland (Hybrid - 2 days working from home) Contract Type: Full-time, Permanent About Brenntag UK & Ireland: Brenntag UK & Ireland is part of the global Brenntag Group, the world’s leading distributor of chemicals and ingredients. Headquartered in Leeds, we operate across 21 strategic...

This multinational pharmaceutical and biotechnology corporation is one of the largest producers of therapeutics in the world, with upwards of 70,000 employees and revenues above 10 billion per annum. In recent years, this market leader has expanded its footprint in Ireland, to not only include significant manufacturing operations, but additionally has...

Company 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),...

Other responsibilities include: Attending trade association meetings Managing and growing a succesful team Ensuring all product claims, marketing materials and website sell copy are legally compliant Offering regulatory advice to multiple departments Supporting NPD by providing expert regulatory guidance on new and innovative formulations Maintaining...

A leading medical communications firm in Leeds is seeking a Senior Regulatory Writer to craft and review high-level regulatory documents for global submissions. The ideal candidate will develop high-quality regulatory documents and lead complex submissions while mentoring junior writers. With a degree in life sciences and experience in regulatory writing,...

**Description** Are you passionate about ensuring healthcare technology meets the highest regulatory standards? Do you have a strong background in compliance and a keen eye for detail? If so, we have an exciting opportunity for you to join our Audit, Compliance & Certification team as a **Regulatory Compliance Officer**. At System C, we are dedicated to...