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Social network you want to login/join with: Regulatory Affairs Manager - Pharmaceuticals As the Regulatory Affairs Manager for the UK and Ireland, you will provide expert regulatory guidance to our UK organization and manage all regulatory activities across the UK and Ireland. With several exciti...

Planet Pharma is partnering with a pharmaceutical client seeking to hire a Senior Project Manager to oversee the setup, execution, and management of Expanded Access Programs (EAP) and Post-Approval Named Patient Programs (PA-NPP). Key Responsibilities: - Manage the start-up, execution,...

Job Title: Department Leader – Regulatory Affairs– IVDs Job Type: Full-Time, permanent position Location: Outskirts of Edinburgh, Scotland, UK – (1 week per month on site) Remuneration: £80,000 – £90,000 + benefits The role is a full-time, permanent position working 37.5 hours per week. R...

The Department Leader for Regulatory Affairs is also responsible for acting as an active participant in team meetings that relate to changes to developed products that will require further registration and regulatory submissions. The Department Leader is also responsible for managing and supporti...

Social network you want to login/join with: Job Title: Customer & Market Insights Innovation Lead Location : Reading - Awaiting confirmation on any onsite requirements Sector : Global Biotech FTE: 3 days per week (may flex to 4/5 during busy periods if possible) Role Summary We’re looking for an ...

Disease Area Medical Lead – Ophthalmology Biopharma Company | United Kingdom Reporting to: UK Medical Affairs Leadership Location: United Kingdom Summary A leading global biopharmaceutical company focused on retinal disease is seeking a Disease Area Medical Lead to head its strategic ...

This role is open for candidates in EU/UK only. Applications from other locations will not be considered About the job About Freyr Freyr is a fast-growing, innovative company specializing in providing end-to-end regulatory solutions and services for the Life Sciences industry. With a co...

Medical Information Specialist (Maternity Cover for 1 year- Starting Late September/ Early October 2025) Who are we? We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth op...

Medical Affairs Manager – Healthcare/Pharma 📍 Remote | UK-wide 💰 £70,000 - £95,000 plus car allowance and benefits or 💰 £600 - £650 per day (Outside IR35) An exciting opportunity for an experienced Medical Affairs professional to join an innovative, fast-growing healthcare comp...

Associate) Director, Clinical Affairs – Infectious Diseases | Global IVD Focus 📍 Remote – UK or France | Permanent Position A global diagnostics company is seeking an experienced Clinical Affairs leader to head their infectious disease clinical programme, supporting the development and global...

As an Innovation Strategy Consulting Manager, you will play a pivotal role in delivering high-impact projects from end-to-end, managing a team of consultants, and supercharging the growth of our Consultancy practice. Working directly with the Head of Consulting, you will take ownership of bu...

Job Summary: We are seeking an experienced and driven Senior PK/PD Modeller to join our Clinical Pharmacology team. In this role, you will be responsible for the design, development, and implementation of pharmacokinetic/pharmacodynamic (PK/PD) modeling strategies to support drug development ...

Are you an experienced QA/RA leader ready to shape the future of wound care? A pioneering MedTech start-up is seeking a Quality Assurance and Regulatory Affairs Manager to drive global regulatory strategy and quality systems for an innovative Advanced Tissue Repair Platform targeting chronic and...

Regulatory Consultant – Electronic Medical Devices (IEC 60601 Focus) Remote (UK or Ireland based) | Circa £60,000 – £70,000+ - Applicants must have the right to work in the UK or Ireland and either already be residing there or have a clear, committed plan to relocate. - This role requires in...

Blatchford is a multi-award-winning, global, manufacturer of some of the world’s most advanced prosthetic technology, bespoke seating solutions and orthotic devices. Our evidence-based approach and commitment to continuously challenge possibilities ensures our mobility solutions prioritise the ...

- Job Title: Senior Post Market Surveillance Specialist - Contract: until 31/1/26 - Location: Remote - Pay: £153 per day SRG are partnered with a global medical products and technologies company. Our client is focused on solutions for the management of chronic conditions, with leadi...

A pioneering biotech focused on individualized therapies for rare pediatric neurodegenerative conditions is seeking a Senior Vice President / Vice President of Regulatory Affairs. This executive role will lead global regulatory strategy, with a particular focus on the UK and EU, supporting the d...

Senior Vice President / Vice President of Regulatory Affairs. Proven leadership in EU/UK submissions and regulatory agency engagement. This executive role will lead global regulatory strategy, with a particular focus on the UK and EU, supporting the development of advanced genetic therapies using...

Provide critical support in developing global regulatory strategy, planning and execution of global investigational submissions and manages lifecycle regulatory activities in alignment with the Global Regulatory Lead (GRL). Research and apply regulatory intelligence and knowledge of strategic opt...

The Department Leader for Regulatory Affairs is also responsible for acting as an active participant in team meetings that relate to changes to developed products that will require further registration and regulatory submissions. The Department Leader is also responsible for managing and supporti...

Regulatory Affairs Manager in the preparation and submission of documents for regulatory agencies. Previous experience in regulatory affairs in the medical device industry. Assisting with the preparation and submission of regulatory documents to regulatory agencies.

Regulatory Affairs Manager in the preparation and submission of documents for regulatory agencies. Assisting with the preparation and submission of regulatory documents to regulatory agencies. Previous experience in regulatory affairs in the medical device industry.

Regulatory Affairs Manager in the preparation and submission of documents for regulatory agencies. Previous experience in regulatory affairs in the medical device industry. Assisting with the preparation and submission of regulatory documents to regulatory agencies.