Latest Professional Services Jobs

Regulatory Intelligence Lead - Biologics/Vaccines

Leads global regulatory intelligence strategy for biologics and vaccines, interpreting evolving cGMP regulations and shaping policy to support Pfizer’s quality and compliance standards. Represents the company in international forums, influences regulatory guidelines, and drives digital transformation of intelligence capabilities. Works across global teams to ensure alignment on compliance and quality initiatives for innovative therapies.

Pfizer Belgium

On-site Permanent

Regulatory Intelligence Lead - Biologics/Vaccines

Leads global regulatory intelligence strategy for biologics and vaccines, interpreting evolving cGMP regulations and shaping policy to support Pfizer's compliance and innovation goals. Represents the company in international forums, influences regulatory standards, and drives digital transformation of intelligence capabilities. Works across quality, regulatory, and technical teams to ensure global alignment and inspection readiness.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Global Program Safety Team Lead

This role involves leading the Medical Safety organization for Novartis' Neuroscience division, managing safety strategies, and influencing high-stakes decisions. Responsibilities include managing disease areas, enhancing team expertise, and ensuring robust safety evaluations throughout the product lifecycle.

Novartis United Kingdom

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing compliance oversight for clinical programs and trials, ensuring adherence to Good Clinical Practice standards. You will act as a primary compliance partner to Clinical Trial Teams, enabling decision-making on complex regulatory scenarios and leading cross-functional discussions to resolve quality issues.

Novartis Ireland

Hybrid 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

Medical Devices Project Leader - Cambridge

Medical Devices Project Leader - CambridgeWe are seeking a dynamic and driven Project Leader to join our innovative medical devices team based in Cambridge. This is a unique opportunity to lead cutting-edge development projects that directly impact patient care and...

Newton Colmore Cambridge, United Kingdom

Permanent

Senior Biomedical Scientist

This role involves performing full blood count analysis and using LC-MS/MS to monitor clozapine and other antipsychotic medications in a specialist pathology laboratory. The scientist will manage laboratory information systems, ensure data accuracy, and maintain quality control standards. The position also includes contributing to SOP development, method improvement, and broader lab operations such as supply chain and IT support.

Reed Specialist Recruitment Hereford, Herefordshire, United Kingdom

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

PKPD Modelling Lead, London

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...

Isomorphic Labs London, United Kingdom

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, and ensuring adherence to quality standards across global clinical programs. The manager will lead investigations into quality issues, drive inspection readiness, and translate regulatory requirements into practical actions. Collaboration with cross-functional stakeholders is central to strengthening compliance and fostering a culture of data integrity and accountability.

Novartis London, United Kingdom

Hybrid Permanent

Scientist / Senior Scientist, Computational Biology

This role involves designing and executing computational strategies to analyze large-scale omics data, developing robust bioinformatic pipelines, and collaborating with cross-functional teams to advance aging and rejuvenation research. The position requires a PhD in Life Science or Computational Biology, with a focus on high-throughput data analysis and strong programming skills.

Altos Labs Cambridge, United Kingdom

On-site Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, leading quality issue resolution, and ensuring inspection readiness across global clinical programs. The manager will translate regulatory requirements into actionable insights, conduct self-assessments, and drive continuous improvement in compliance. Embedded within cross-functional teams, the role emphasizes proactive risk mitigation, data integrity, and collaboration with Quality Assurance and Development functions.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Hybrid Permanent

Head of MSAT

MSAT ManagerPermanent | Darlington | Up to £70,000About the Role:We are seeking anMSAT Manager to lead technology transfer activities into GMP manufacturing within an advanced biopharmaceutical manufacturing environment.Reporting into the leadership team, this is a highly visible role responsible for...

SRG Darlington, United Kingdom £55,000 – £70,000 pa