Latest Life Sciences Jobs

Spotlight

Lead Development Engineer

This role involves leading the design and development of next-generation orthopaedic implants and instrumentation. Responsibilities include creating detailed designs using CAD, FEA, and PLM, mentoring team members, managing design control documentation, and collaborating with manufacturing, quality, and regulatory teams. The position offers opportunities to work with cutting-edge technologies and contribute to impactful medical innovations.

Corin Group Cirencester, gloucestershire, United Kingdom

On-site Permanent

Project Manager - Clinical Studies (Life Sciences)

This role involves leading sub-workstreams and programs related to clinical operations integration, divestment, and partnerships. Responsibilities include developing processes, managing working groups, and acting as a subject matter expert on study-level integration and separation activities.

Experis London, United Kingdom £650 – £700 pd

Senior Pharmacovigilance Scientist - Signal management / RMP

The Senior Pharmacovigilance Scientist will lead safety signal management activities, including detection, evaluation, and assessment of safety signals. They will also oversee aggregate reports, respond to safety queries, and ensure compliance with global safety regulations and guidelines.

Hays Life Sciences London, City And County Of the City Of London, United Kingdom £60 – £100 ph

Remote Contract

Senior Pharmacovigilance Scientist - Signal Management

The Senior Pharmacovigilance Scientist will lead safety signal management activities, write aggregate reports, and support clinical trial pharmacovigilance. They will also serve as a subject-matter expert on global safety regulations and ensure compliance with regulatory bodies.

Hays Life Sciences London, City And County Of the City Of London, United Kingdom £80 – £109 ph

Remote Contract

Systems Engineer - Automation

As Systems Engineer, you will manage development lifecycle involvement to provide Automated Robotic sample storage systems to deliver cutting edge scientific applications and integrated platforms for biological sample and clinical intelligence.Systems Engineer provide the cohesion and co-ordination between engineering and...

Azenta Life Sciences Partington, Manchester, United Kingdom

Senior Systems Engineer

As Senior Systems Engineer / Senior Product Development Engineer you will manage development lifecycle involvement to provide Automated Robotic sample storage systems to deliver cutting edge scientific applications and integrated platforms for biological sample and clinical intelligence.Systems Engineer provide the...

Azenta Life Sciences Partington, Manchester, United Kingdom

Territory Account Manager - Southern England

This role involves driving commercial growth across Southern England by developing new business opportunities and expanding existing customer relationships within the life sciences sector. The focus is on engaging with pharmaceuticals, biotech, CROs, healthcare, and research organizations, fostering long-term commercial relationships and managing complex sales cycles.

Big Red Recruitment Midlands Limited Milton Keynes, Buckinghamshire, United Kingdom £60,000 – £65,000 pa

On-site Permanent

HCP Liaison Manager

Talentmark are working in partnership with a leading UK life sciences biotechnology company, to recruit for an experienced HCP Liaison Manager to join them at their site based in London. This is a hybrid field- and office-based position, requiring regular...

Talentmark London, United Kingdom

Project Consultant

As a Project Consultant for Patient Cloud, you will manage client relationships and oversee the delivery of high-quality projects across various stages. Your responsibilities include leading cross-functional teams, managing project timelines, and ensuring successful outcomes for clinical research and SaaS technology initiatives.

Randstad Engineering London, United Kingdom

Remote Permanent

Automation Engineer - Pharmaceutical

This role involves maintaining and troubleshooting automation and control systems in a GMP-regulated pharmaceutical manufacturing environment. You will participate in computerized system validation, support continuous improvement projects, and collaborate with cross-functional teams to ensure compliance and data integrity.

Smart4Sciences West Yorkshire, United Kingdom

On-site Permanent

Business Analyst

The Business Analyst will support a key programme focused on the collection, tracking, and lifecycle management of human biological samples. Responsibilities include eliciting and documenting requirements, mapping end-to-end processes, and facilitating workshops with scientific and technical teams to enhance biobanking systems and data flows.

DCV Technologies Stevenage, Hertfordshire, United Kingdom £400 – £450 pd

Hybrid Contract

Mechanical Engineer - Genomics Instrumentation - Cambridge

You will work within a multidisciplinary team to design and develop cutting-edge genomics instrumentation, contributing to high-throughput genomic workflows and precision diagnostics. Your role involves the full product lifecycle, from concept development to product launch.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Biomedical Engineer

This role involves on-site and remote troubleshooting, installation, maintenance, and repairs of medical equipment. You will complete preventative maintenance and field modifications, working independently to support customers efficiently within your assigned territory.

FIELD Bristol, Bristol (county), United Kingdom £35,000 – £40,000 pa

On-site Permanent

Medical Device Engineer

This role involves troubleshooting, installing, maintaining, and repairing medical equipment both onsite and remotely. The engineer will work independently within an assigned territory, completing preventative maintenance and field modifications, while collaborating with a larger team to provide efficient service support.

FIELD Bristol, Bristol (county), United Kingdom £35,000 – £40,000 pa

Hybrid Permanent

Quality Engineer, Validation

The Quality Engineer, Validation is responsible for ensuring robust and repeatable manufacturing processes and test methods, leading validation activities for new and existing processes. This role involves close collaboration with Design Assurance, Operations, and Suppliers to develop validation plans, execute validation phases, and ensure compliance with ISO standards and regulatory requirements.

OrganOx Oxford, United Kingdom

On-site Permanent

Process Engineer, Validation

The Process Engineer, Validation leads and executes validation activities for new product ranges and changes to existing medical devices. They ensure all manufacturing processes, equipment, and test methods meet internal and external regulatory standards, working closely with cross-functional teams and external partners. The role involves developing validation strategies, authoring protocols, conducting risk assessments, and supporting regulatory submissions.

OrganOx Oxford, United Kingdom

On-site Permanent