Latest Biotech Jobs

Principal Mechanical Design Engineer - Medical Devices

Principal Mechanical Design Engineer - Medical Devices - CambridgeA growing Medical Devices team, based in Cambridge, is currently seeking an experienced Mechanical Design Engineer to lead the development of cutting-edge Medical Devices in the fields of Health Technology, Biotech, and...

Newton Colmore Cambridge, United Kingdom

Permanent

Application Engineer

The role involves supporting technical sales and customer relationships for a biotech engineering consultancy specializing in microfluidic systems. The Application Engineer will manage customer enquiries, prepare quotations, coordinate project pricing, and provide post-sales support, while collaborating with engineering teams to meet client needs. The position includes opportunities to engage with international clients and represent the company at trade shows and conferences.

Jackson Hogg Gateshead, Tyne & Wear, United Kingdom £30,000 – £32,000 pa

Transport Operator

The Transport Operator ensures smooth daily transport operations by managing delivery scanning, manifesting, and tracking in compliance with SOPs and regulations. You'll support drivers through briefing and debriefing using transport management systems, resolve delivery issues, maintain customer communication, and uphold health and safety and DVSA compliance standards. The role involves administrative coordination, incident reporting, and cross-dock activity within a pharmaceutical logistics environment.

Movianto Dartford, United Kingdom £27,970 pa

On-site Permanent

Van Driver

As a Van Driver at Movianto, you will deliver pharmaceutical products efficiently and safely, ensuring compliance with health and safety regulations. You will operate company vehicles, perform daily maintenance checks, and maintain a professional image while adhering to legal requirements and company policies.

Movianto Slough, United Kingdom £29,467 pa

On-site Permanent

Technical Service Engineer

This role involves providing on-site and remote technical support for advanced robotics solutions in the pharmaceutical and biotechnology sectors. As the primary Field Service Engineer for the Manchester area, you'll perform diagnostics, preventative maintenance, and customer training, while collaborating with R&D and sales teams. The position includes 24/7 on-call responsibilities, extensive product training, and occasional travel beyond the local region.

Wallace Hind Selection Manchester, United Kingdom £52,000 – £56,000 pa

Technical Service Engineer

This role involves providing on-site and remote technical support for advanced robotics systems used in pharmaceutical and biotechnology environments. The engineer will act as a subject matter expert, performing diagnostics, preventative maintenance, and resolving service issues in collaboration with customers and internal teams. The position includes 24/7 on-call responsibilities and extensive training on proprietary systems, serving the Manchester area with occasional travel.

Wallace Hind Selection Marston, Cheshire West And Chester, Cheshire, United Kingdom £52,000 – £56,000 pa

Quality Assurance Officer

This role involves reviewing batch manufacturing and packaging records to ensure compliance with GMP standards prior to product release, supporting batch release activities, and collaborating with external manufacturing partners and internal teams. The candidate will maintain quality documentation and ensure adherence to the Quality Management System within a virtual pharmaceutical model. The position offers hybrid working and is part of a supportive Quality team in a growing organisation with a diverse product portfolio.

Walker Cole International London, United Kingdom £30,000 – £35,000 pa

FPGA Electronics Engineer - Defence - Cambridge

This role involves working on challenging engineering problems in UK defence and national security, focusing on FPGA design and development. You'll collaborate closely with a multidisciplinary team to build solutions from concept to prototype, tackling complex issues in areas like DSP, embedded systems, and advanced communications.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent Clearance Required

Production Operator

Operate packing processes in a regulated medical manufacturing environment, following SOPs, GDP, and GMP standards. Responsibilities include batch documentation, equipment fault reporting, quality communication, and maintaining a clean, compliant workspace. Work collaboratively with QA and adhere to health and safety protocols in a stable, long-term temporary role.

grw talent Livingston, West Lothian, EH54 6GS, United Kingdom £13 ph

On-site Temporary

Manager Global Regulatory Scientist, Regulatory Affairs

This role involves leading regulatory strategy and submissions for global health authorities, including drafting applications like INDs, CTAs, and NDAs/MAAs. The candidate will provide expert regulatory guidance across product development stages, support agency interactions, respond to queries, and ensure compliance with FDA, ICH, and other global regulations. With a focus on oncology and combination products, the position requires strategic input, cross-functional collaboration, and lifecycle management across pharmaceuticals, devices, and biologics.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Manager Global Regulatory Scientist, Regulatory Affairs

This role involves leading and supporting global regulatory submissions for pharmaceutical, device, and combination products, with responsibilities spanning IND/CTA/MAA preparation, health authority interactions, and lifecycle management. The candidate will advise cross-functional teams on regulatory strategy, ensure compliance with FDA, ICH, and other global regulations, and contribute to responses to agency queries, particularly in oncology and novel product areas with limited regulatory precedent.

Johnson & Johnson MedTech Belgium €79,800 – €137,770 pa

Mgr Global Regulatory Scientist, Reg Aff

This role involves providing regulatory support for global submissions and interactions with health authorities, including preparing applications (IND, CTA, NDA, MAA), advising on regulatory strategy, and ensuring compliance across pharmaceutical, device, and combination product types. The position requires close collaboration with cross-functional teams and local regulatory colleagues to manage life cycle submissions and respond to agency queries. It offers exposure to oncology and novel product areas with limited regulatory precedent.

Johnson & Johnson MedTech US$117,000 – US$201,250 pa