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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 exciting drug launches planned over the next 24 months, we are looking for a dedicated and expe...

Planet Pharma are partnered with a leading pharmaceutical company and we are actively seeking an experienced Senior Manager Regulatory Affairs to join the business on an initial 12 month contract basis. Shape and implement regional regulatory strategy by advising the Global Regulatory Team (GRT),...

Planet Pharma are currently working on an exciting opportunity with a global biopharmaceutical company that’s looking to expand its Regulatory Affairs team. As a key member of the global regulatory project team, you’d play a strategic role in shaping submission strategies and ensuring compliance

As we expand our footprint , we are on the lookout for passionate and skilled Regulatory professionals to join us in shaping the future of regulatory services. Let's redefine regulatory excellence together!. Experience : 5 years in Medicinal Products Regulatory Affairs with 2 years in Project Man...

Social network you want to login/join with: col-narrow-left VRS Regulatory Other - Yes col-narrow-right 4 31.05.2025 15.07.2025 col-wide An opportunity to join the EU Regulatory Affairs team at a global disinfectant products manufacturing company. You will work alongside an experience...

Social network you want to login/join with: Crinetics is a pharmaceutical company based in San Diego, California, USA, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that ...

Social network you want to login/join with: col-narrow-left Warman O'Brien Other - Yes col-narrow-right 2 31.05.2025 15.07.2025 col-wide Associate Director, Field Medical Advisor Remote, UK Start Date: ASAP Join a biotech leader driving the future of mRNA-based therapies with a div...

Are you passionate about delivering exceptional client service in the financial services sector? At Mattioli Woods, we’re looking for a proactive and detail-focused Financial Services Administrator to join our team in Leicester. This is an exciting opportunity to support advisers and Client Rel...

Planet Pharma are partnered with a leading biotech and we are actively seeking an experienced QC Technician to join the business on an initial 6 month contract. Key Responsibilities: - Ensure compliance with GMP, GDP, and internal quality standards across laboratory and manufacturing opera...

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 Medical Writer As a Senior Medical Writer, you’ll contribute to a variety of projects across therapy areas, translating complex science into clear, engaging content. With a solid scientific foundation and strong writing skills, you’ll produce client-ready materials, support scientific co...

A leading UK law firm is seeking an experienced and dynamic Partner to head up its nationally recognised Court of Protection – Property & Affairs team. This is a senior leadership opportunity for an accomplished Solicitor with a passion for client care, team development, and strategic growth. Th...

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 ...

This temporary 12-month position (for maternity cover) reports to the Manager of Quality Assurance (Design) and is part of the Quality Assurance and Regulatory Compliance Department located in Newcastle-upon-Tyne and will be an on-site position. In this role, you will have the opportunity t...

!*Market Research & Insights Specialist - Fully remote in UK - Leading Bio-Pharmaceutical!* Location: Homebased in the UK FTE: Freelance (Company average tenure is 4+ years) Start date: ASAP Rate: Very good rate Job Description Planet Pharma are working with a global biopharmaceu...

An opportunity to join the EU Regulatory Affairs team at a global disinfectant products manufacturing company. You will work alongside an experience regulatory manager who will provide training where needed; your role will be to work on preparing dossiers for biocide products via the national/tr...

Now Hiring: Head of Medical Affairs – Full lifecycle Hybrid (2 days office-based) Exclusive with CK Group This is a role within a dynamic pharmaceutical company moving into a pre-launch setting and exciting new phase of growth who are looking for a strategic and operational leader to head...

If you are a seasoned Regulatory professional within the Medical Device space, this role might be for you! We’re looking for a Regulatory Consultant who can support a diverse portfolio of clients with particular expertise in medical device software (SaMD) and AI/ML technologies. Prepare and revie...

Senior Vetting Officer (12 month FTC) Base Location: Watford / Birmingham (with intermittent travel to other UK offices including Canary Wharf) The KPMG Business Services function is a cornerstone of our UK business. Operating from 20 UK locations and sitting with KPMG Central Services w...

Mantell Associates are proudly partnered with a Globally recognised CDMO in their search for a Principal Analyst (Spectroscopy) to join their team. Principal Analyst (Spectroscopy) - Responsibilities: - Lead and manage spectroscopy-based analytical methods (UV-Vis, IR, NMR, MS) to suppo...

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 commitment to excellence and innovation, we assist pharmaceutical, medical device, and biotech companies in navigating the comple...

Base Location: Watford / Birmingham (with intermittent travel to other UK offices including Canary Wharf) The KPMG Business Services function is a cornerstone of our UK business. Operating from 20 UK locations and sitting with KPMG Central Services we do work that matters. Within Central Se...

Crinetics is a pharmaceutical company based in San Diego, California, USA, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous inno...

Location Remote, with expectation for attendance in the office for team meetings (approx. every two months) Employment Type Full-Time, Permanent About Us Are you interested in working with pioneers in the field of AI and software engineering? Are you interested in working with some of the world...

We are looking for an Endocrine Disruption Specialist/Expert to join an experienced multi-disciplinary team working in the field of chemical regulatory science; you will work alongside two well-known Endocrine Disruption experts providing specialised services to pharma, industrial chemical, cr...

Senior Regulatory Affairs Manager - Emerging Markets. We are currently looking for a Snr Regulatory Affairs Manager with experience in Emerging Markets including Middle East Africa (MEA), Turkey, CIS & Russia (TCR) and Central Eastern European Markets (CEE). Responsible for development and delive...

Sick of soul-sucking paraplanning gigs where your talent goes unnoticed and your ideas die in someone else’s inbox? At Vital Financial Planning, we’re building something fresh. We’re young. We’re growing. And we’re flipping the script on what a modern financial planning firm should look and ...

Quality Assurance, Regulatory Affairs, Sustainability, and Legal. Lead the Compliance function across Quality Assurance, Regulatory Affairs, Sustainability, and Legal. Reporting to the C-Suite, this senior leadership role ensures that all operations, products, and services comply with applicable ...

Role: Market Research & Insights Consultant Location: Remote, UK Company: Global Pharmaceutical (Industry experience is required) We are working with a Global Pharmaceutical company who are currently looking for a Market Research & Insights Consultant to join them on a freelance basis work...

Minimum 10+ year experience in regulatory affairs with experience in the food industry and an understanding of related issues. Head of Regulatory Affairs, EMEA. Develop and implement policies and procedures for regulatory affairs.

As Regulatory Affairs Advisor for one of their flagship European projects, you'll support the leadership team with expert guidance on regulatory developments affecting German and wider EU energy markets. Regulatory Affairs Advisor - Electricity Markets.

Planet Pharma are currently working on an exciting opportunity with a global biopharmaceutical company that’s looking to expand its Regulatory Affairs team. If you have 3–5+ years’ experience in regulatory affairs, particularly in emerging markets, and enjoy cross-functional collaboration with

As Regulatory Affairs Advisor for one of their flagship European projects, you'll support the leadership team with expert guidance on regulatory developments affecting German and wider EU energy markets. Regulatory Affairs Advisor - Electricity Markets.

If you are a seasoned Regulatory professional within the Medical Device space, this role might be for you! We’re looking for a Regulatory Consultant who can support a diverse portfolio of clients with particular expertise in medical device software (SaMD) and AI/ML technologies. Develop and imple...

As Regulatory Affairs Advisor for one of their flagship European projects, you'll support the leadership team with expert guidance on regulatory developments affecting German and wider EU energy markets. Regulatory Affairs Advisor - Electricity Markets.

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Senior Regulatory Affairs Manager - Emerging Markets. We are currently looking for a Snr Regulatory Af...

Reporting to the Regulatory Affairs Manager, this strategic position involves preparing and submitting regulatory applications in key markets in the EU, acting as Project lead in support of the new product development programme and renewal of existing product authorisations. The ideal candidate w...

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 development of advanced genetic therapies using ASO technologies. Lead regulatory strategy and submissions across the UK...

As Regulatory Affairs Advisor for one of their flagship European projects, you'll support the leadership team with expert guidance on regulatory developments affecting German and wider EU energy markets. If you are a regulatory affairs professional eager to shape the future of energy markets in G...

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. Regulatory Affairs Manager - Pharmaceuticals. With several exciting drug launches planned over the next 24 m...

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Planet Pharma are partnered with a leading pharmaceutical company and we are actively seeking an exper...

Planet Pharma are currently working on an exciting opportunity with a global biopharmaceutical company that’s looking to expand its Regulatory Affairs team. If you have 3–5+ years’ experience in regulatory affairs, particularly in emerging markets, and enjoy cross-functional collaboration with

Minimum 10+ year experience in regulatory affairs with experience in the food industry and an understanding of related issues. Head of Regulatory Affairs, EMEA. Develop and implement policies and procedures for regulatory affairs.

If you are a seasoned Regulatory professional within the Medical Device space, this role might be for you! We’re looking for a Regulatory Consultant who can support a diverse portfolio of clients with particular expertise in medical device software (SaMD) and AI/ML technologies. Provide regulator...

If you are a seasoned Regulatory professional within the Medical Device space, this role might be for you! We’re looking for a Regulatory Consultant who can support a diverse portfolio of clients with particular expertise in medical device software (SaMD) and AI/ML technologies. Develop and imple...

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Planet Pharma are partnered with a leading pharmaceutical company and we are actively seeking an exper...

Ownership of Conduct Risk and Consumer Duty frameworks Managing of Conduct and Complaints team Adherence to Lloyd's and FCA regulatory requirements 5+ years' experience working in a relevant Conduct Risk role ~ Commercial and pragmatic individual who enjoys building relationships ~.

About the Role The Compliance and Risk officer is responsible for identifying and mitigating compliance risks, ensuring adherence to UK regulatory frameworks, including GDPR, the Office for Students (OfS) requirements, and internal policies. Responsibilities: Lead and oversee all aspects of hig