Latest Medical Services Jobs

NPI Quality Engineer

This role involves leading quality assurance throughout the new product introduction (NPI) process in a high-tech manufacturing environment. The engineer will ensure compliance with quality standards across design, development, and production, working closely with engineering, R&D, and supply chain teams. Key responsibilities include managing APQP/PPAP deliverables, leading root cause investigations, and driving continuous improvement in quality processes.

Yolk Recruitment Briton Ferry, West Glamorgan, SA11 2NH, United Kingdom £45,000 pa

On-site Permanent

Pharmaceutical/Healthcare Sustainability Lead

We are partnering with a leading organisation in the Pharmaceutical, Healthcare and Retail Eye Care market, to recruit an impactful Pharmaceutical/Healthcare Sustainability Lead who will shape and drive the company’s environmental strategy. In this role, you’ll work closely with senior...

Evolve Selection Birmingham, West Midlands (county), United Kingdom £55,000 – £60,000 pa

Manufacturing Engineer

Manufacturing Engineer | Sheffield | £40,000-£50,000 + BenefitsW Talent is delighted to be partnering with a leading advanced manufacturing business in Sheffield to recruit a Manufacturing Engineer.This is an exciting opportunity to join a highly respected engineering organisation where you'll...

W Talent Sheffield, South Yorkshire, United Kingdom £40,000 – £50,000 pa

Global Labelling Director, Content (Immunology)

The Global Labelling Director, Content (Immunology) will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include developing core labelling documents, collaborating with cross-functional teams, and ensuring compliance with regulatory requirements. The role involves representing global labelling in governance forums and contributing to decision-making discussions.

Novartis

Hybrid Permanent

Head of Global Regulatory Affairs and Strategy, Cambridge, MA

This senior leadership role involves defining and optimizing global regulatory strategies for drug development programs, building a regulatory team and systems, and implementing quality, pharmacovigilance, and medical writing frameworks. The role leverages AI to streamline regulatory workflows and ensure rapid global approval of products.

Isomorphic Labs Cambridge, United Kingdom

On-site Permanent

Principal Scientist Biosensors

Are you an experienced R&D scientist with a background in biosensors, electrochemistry or diagnostic assay development? Are you looking to take the next step into a scientific leadership role within a rapidly growing, innovation-driven organisation?We're partnering with an exciting nanotechnology...

VRS UK Stirling, Stirling And Falkirk, United Kingdom £70,000 – £86,000 pa

Senior Safety Scientist / Associate Director / Director

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive...

Roche Welwyn Hatfield, United Kingdom

Warehouse Operative

Warehouse Operative – Warrington (WA5)Aspired Talent£13.00 per hour | £13.50 per hour with a Counterbalance FLT LicenceMonday to Friday | 8:00am – 4:30pmTemp to Perm OpportunityAspired Talent is recruiting for an experienced Warehouse Operative to join our client in Warrington...

Aspired Talent Ltd Great Sankey, Cheshire, United Kingdom £13 – £14 ph

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves strategic planning, innovative thinking, and engagement with external stakeholders to drive the clinical development program.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves strategic planning, regulatory submissions, and engagement with external stakeholders to drive the clinical development program.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Senior Electrical Design Engineer

A leading engineering organisation in Bristol is seeking a Senior Electrical Design Engineer to take ownership of complex electrical system design across a range of innovative projects. This role suits someone who thrives on technical depth, precision, and delivering high‑quality...

Verso Recruitment Bristol, Bristol (county), United Kingdom £50,000 – £60,000 pa

Chemical Process Operator

This role involves operating chemical process plant and manufacturing equipment, following batch manufacturing instructions, monitoring chemical reactions, and supporting material handling and packaging activities. The position offers long-term stability and development opportunities within a safety and quality-driven manufacturing environment.

Talent STEM Ltd Stradishall, United Kingdom

On-site Permanent Shift-work

Lead Electronics Design Engineer

Lead the design and development of high-precision electronic systems for next-generation life science instruments, focusing on low-noise analogue circuits and system integration. Lead a team of engineers while remaining hands-on with PCB design, signal integrity, and debugging. Collaborate across disciplines to deliver advanced sensing platforms from concept to commercialisation.

Tec Partners Recruitment Ltd Notting Barns, London, United Kingdom £80,000 – £100,000 pa

On-site Permanent

Regulatory Affairs Specialist

The role involves providing technical regulatory support for the international distribution of diagnostic products, ensuring compliance with CE marking and global medical device regulations. Responsibilities include validating product claims, maintaining up-to-date documentation, and reviewing complaints for regulatory reportability. The position is based at the Innovation Centre in Bedford with hybrid working options.

Swiss Precision Diagnostics GmbH Cardington, Bedfordshire, United Kingdom £30,000 – £35,000 pa

Hybrid Contract

Clinical Development Director - Renal

The Clinical Development Director is responsible for leading and supporting the delivery of clinical deliverables for a section of a global clinical program or a large, complex trial. This role involves collaborating with various teams to ensure data quality, regulatory compliance, and scientific accuracy in clinical trials and publications.

Novartis London, United Kingdom

Hybrid Permanent