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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...

Regulatory Affairs and Risk Assessment division of specialist scientific recruiter VRS.

Advise internal stakeholders on regulatory risks and compliance. Represent the company in external regulatory forums and industry groups. Scale regulatory operations during rapid organizational growth.

A fast-growing and forward-thinking life sciences consultancy is seeking an Associate Director of Regulatory Affairs – CMC to lead regulatory strategy and execution across a dynamic portfolio of biologic and advanced therapy programs. As an Associate Director, you will work directly with biotech ...

We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology and Environmental Fate in the chemicals, agrochemicals and biocides sectors. We are looking for an Endocrine Disrup...

Shape and implement regional regulatory strategy by advising the Global Regulatory Team (GRT), ensuring regional requirements are fully integrated and aligned with global development goals. Planet Pharma are partnered with a leading pharmaceutical company and we are actively seeking an experience...

Job Title: Director of Compliance.A leading healthcare company dedicated to placing patients at the centre of everything it does is seeking a seasoned and visionary.Quality Assurance, Regulatory Affairs, Sustainability, and Legal.They have a strong international presence and an expanding portfoli...

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...

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...

Where your expertise isn’t just valued—it’s driving the next evolution of technical and non-technical hiring. At Bitfinex, we’re not just building teams—we’re redefining how talent acquisition works in a remote-first, innovation-driven environment. We’re looking for a Senior Recruiter with a gl...

Social network you want to login/join with: col-narrow-left VRS Regulatory glasgow, United Kingdom 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 wor...

This is a Temporary, Full-Time vacancy that will close in 25 days at 23:59 BST. We’re seeking an enthusiastic Senior Press Officer to join our in-house PR team for a 12-month maternity cover contract. The role is within an energetic, integrated marketing team of 29, collaborating closely with ...

Birmingham, England, United Kingdom; Glasgow, Scotland, United Kingdom; London, England, United Kingdom; Manchester, England, United Kingdom; Remote; UK Company Overview Throughout our worldwide network of experts, clients and communities, we are renowned for our leadership in fire protection ...

EMEA Human Capital Management – EMEA Wellbeing and Benefits, Director (AVP equivalent) Location: Glasgow JR005935 We’re seeking someone to join our team as an EMEA Wellbeing and Benefits Director within the Human Capital Management division. In the Human Capital Management division, we prov...

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 ...

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...

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...

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...

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 ...

Medical Affairs Advisor – European Focus - Fixed Term Contract (1 year) Overview A leading pharmaceutical organisation is looking for a Medical Affairs Advisor to join it's European medical team. Supporting the Medical Director, this is person will act as a key conduit between the external h...

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...

Associate Director, Field Medical Advisor Remote, UK Start Date: ASAP Join a biotech leader driving the future of mRNA-based therapies with a diverse pipeline targeting major health challenges. We are seeking an experienced Field Medical Advisor with a strong vaccines background to play a ...

Global Regulatory Lead / Associate Director - Regulatory Affairs. 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. Experience leading a broad range of regulatory activities and setting t...

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

My client are looking for an experience CSV Auditor , The main task is to manage and perform audits with focus on Computer System Validation (CSV) audits. The role is offered on a 1 year contract . The role is based in the UK and will involve travelling to sites across Europe . Additio...

Mackenzie Stuart is partnering with a global speciality manufacturer specialising in the Food and and Beverage Ingredients sector. Looking to expand in the US market, this organisation is in need of a Head of Regulatory Affairs, EMEA. This lead position is a key partnership role engaging fu...

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...

We are looking for a scientific leader to manager early-stage product innovation at a well-known global chemical products business. You will manage an experienced team and provide leadership in the areas of stakeholder relations, innovation and provision of expertise to the wider company. 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...

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 world-renowned Chemical Manufacturer, celebrated for its cutting-edge product development and commitment to sustainability, is seeking an experienced Quality Manager to join its dynamic team at the Blackpool site. With a presence across multiple high-impact sectors - including aerospace, auto...

🚀 Join a Global Leader in mRNA Innovation – Now Hiring: Manufacturing Associate About the Client Our client is at the forefront of mRNA technology, driving innovation in vaccine and therapeutic development. With a growing global presence and a commitment to public health, they are establi...

Head of Stakeholder Engagement and Communications The Resolute Group are working in partnership with a client operating across the Transportation sector, collaborating closely with key stakeholders, such as Local Authorities, Train Operating Companies, Network Rail, TfN, and the DfT, to driv...

We are seeking a diligent and detail-oriented Compliance Officer to ensure our food manufacturing operations meet all relevant legal, regulatory, and internal standards. This role is critical in maintaining product safety, quality, and integrity, while also supporting our commitment to continuou...

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...

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...

Job Title: EU Medical Director Department: Medical Affairs Location: UK Reporting to: Vice President, Medical Affairs – Europe Company: Global, Mid-Sized Pharmaceutical Company Role Summary: The EU Medical Director will lead the medical affairs strategy and activities for a product focu...

Lets redefine regulatory excellence together! Title : Global Regulatory Lead / Associate Director - Regulatory Affairs Location : Remote ( Base location should be in UK / EU- preferably in Hungary/ Poland / Romania/ Czech/ Croatia) Experience : Min 8 years of direct experience with Medicinal Prod...

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...

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

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...

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...

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. Liaise with regulatory authorities and maintain up-to-date know...

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...

Role: Senior Regulatory Affairs Manager - Emerging Markets Location: Remote, UK Company: Global Pharmaceutical 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 Europ...

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...

Self-employed Core Delivery Driver.As one of our Self-Employed Core Delivery Drivers you'll enjoy freedom, flexibility and better financial rewards, plus all the support and benefits of being part of our wider Yodel team.You don't need any experience, and the more you deliver, the more you earn.C...

Self-employed Core Delivery Driver.As one of our Self-Employed Core Delivery Drivers you'll enjoy freedom, flexibility and better financial rewards, plus all the support and benefits of being part of our wider Yodel team.You don't need any experience, and the more you deliver, the more you earn.C...