Biotechnology Jobs

Medical Director, Oncology Clinical Development - Hematology

This role involves leading medical oversight and clinical development for oncology and hematology programs, with responsibilities spanning study design, safety monitoring, data interpretation, and regulatory engagement. The Medical Director will collaborate with cross-functional teams and external experts to ensure clinical integrity and patient-centered decision-making in late-stage drug development. The position requires deep expertise in hematology-oncology and experience in Phase I–III trials within a pharmaceutical or biotech setting.

GSK PLN 455,250 – PLN 758,750 pa

Medical Director, Oncology Clinical Development - Hematology

This role involves leading medical oversight in oncology clinical development, focusing on hematology. The Medical Director will guide study design, ensure patient safety, interpret clinical data, and collaborate with cross-functional teams and external experts. It emphasizes physician leadership in trials from Phase I–III, with a strong focus on real-world impact and regulatory engagement.

GSK £222,750 – £371,250 pa

Associate Director, Regulatory Diagnostics

This role involves designing and delivering global regulatory strategies for precision diagnostics, including companion diagnostics and in vitro devices, within drug development programs. The individual will lead regulatory submissions across the lifecycle, engage with health authorities, and ensure compliance with global regulations. Collaboration with cross-functional teams and external partners is central to advancing regulatory plans for innovative diagnostics in a hybrid working environment.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Global Program Regulatory Director

The Global Program Regulatory Director at Novartis leads the development and execution of global regulatory strategies for innovative medicines. Key responsibilities include guiding Health Authority interactions, evaluating regulatory risks, and leading cross-functional teams to drive successful product development and commercialization.

Novartis £83,510 – £155,090 pa

Field Service Engineer, Medical Diagnostic Systems

Provide on-site service, maintenance, and breakdown repair for advanced medical diagnostic systems used in NHS and private laboratories. Work directly with laboratory staff to resolve technical issues and ensure optimal system performance. Receive full product training and support a market-leading provider of diagnostic equipment.

TRS Consulting Falkirk, Stirling And Falkirk, United Kingdom £52,000 pa

Preclinical In-Vitro Toxicology Scientist

This role involves leading in-vitro toxicology studies within a regulated preclinical environment, focusing on assay development and execution for product safety assessment. The scientist will apply advanced cell-based methods including Neutral Red, Ames, and micronucleus assays, interpret complex biological data, and support regulatory submissions. Collaboration with internal teams and external partners is key, alongside method validation and scientific reporting in a quality-assured laboratory setting.

Hudson Shribman United Kingdom £55,000 – £70,000 pa

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Senior Engineer, CSV Validation

This role involves end-to-end ownership of computerised system validation (CSV) for GxP-regulated systems used in the manufacturing and testing of advanced CAR-T cell therapies. The engineer will author and execute validation documentation, ensure compliance with international regulations (e.g. FDA 21 CFR Part 11, EU GMP Annex 11), manage change controls and CAPAs, and support regulatory inspections. The position requires strong technical writing, cross-functional collaboration, and expertise in GAMP 5 and data integrity within a biopharmaceutical context.

Autolus Stevenage, United Kingdom

Global Site and Study Operations Undergraduate

This role involves hands-on experience in clinical trial execution, regulatory documentation, and site operations. The candidate will work closely with experienced managers and teams, gaining insights into multiple therapeutic areas and contributing to process improvements.

Pfizer Sandwich, United Kingdom

Clinical Development Medical Director (MD required)

The Clinical Development Medical Director is responsible for providing medical and scientific oversight for clinical trials, ensuring patient safety, and contributing to the design and execution of clinical studies. They will also participate in safety reviews, interact with healthcare professionals, and support regulatory activities.

Pfizer Marlow, United Kingdom

Project/ Delivery Manager (Bioinformatics Platform)

This role involves overseeing the implementation of a Bioinformatics Platform, coordinating with multiple teams and functions, and ensuring project alignment with organizational goals. Key responsibilities include managing project timelines, facilitating collaboration, and implementing project management best practices.

Carbon 60 Bracknell, Berkshire, United Kingdom £45 – £52 pd

Pharmaceutical Compounding Technician

Operate in a clean room environment to measure, mix, and compound critical medicines, following strict GMP and SOPs. Support production in chemotherapy, CIVAS, and parenteral nutrition units with precision and attention to detail. Work fixed hours with minimal overtime, contributing to life-saving treatments delivered on the same day.

ITH Pharma Middlesex, London, United Kingdom £27,618 pa

Junior Biomedical Engineer

This role involves performing on-site repairs and preventative maintenance on medical equipment within a hospital setting, ensuring compliance with manufacturer guidelines and minimal disruption to clinical operations. The engineer will work closely with clinical teams, manage workloads, and maintain accurate service records. The position supports asset management and requires adherence to strict technical and safety standards.

Focus Resourcing Orpington, London, BR6 0GE, United Kingdom

Pharmaceutical Materials Scientist

This role involves hands-on laboratory work focused on the physical and analytical testing of pharmaceutical materials, including particle size analysis, microscopy, and surface area measurement. The scientist will support development projects and technical investigations, with responsibilities spanning data interpretation, equipment operation, and process troubleshooting. The position is based in Bromborough and supports a growing global testing organisation.

NMS Recruit Ltd t/a Russell Taylor Group Bromborough, Merseyside, United Kingdom £30,000 – £32,000 pa

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Executive Director / Vice President, Business Development

Lead business development strategy to identify and execute strategic partnerships, in- and out-licensing deals, co-developments, and M&A opportunities in oncology and autoimmune disease. Represent Autolus at high-level meetings, build relationships across biotech, pharma, and academia, and collaborate with cross-functional teams to align BD initiatives with corporate goals. Requires deep expertise in biopharma deal-making and strong scientific-business acumen.

Autolus

Business Development Manager, Biomedical Solutions Sales

This role involves managing key customer accounts and driving new business by selling multi-vendor service contracts in biomedical, ultrasound, and endoscopy product lines. The candidate will identify sales opportunities, represent the company at events, and develop proposals to exceed regional targets. It is a home-based position with a focus on relationship-building and market expansion within the healthcare technology sector.

TRS Consulting Reading, Berkshire, United Kingdom £45,000 – £55,000 pa