Biotechnology Jobs

• London
• Hybrid
• US$222,750 – US$371,250 pa
• Director

Leads end-to-end Model-Informed Drug Development and clinical pharmacology strategy across the drug development lifecycle, from first-in-human studies through filing and lifecycle management. Coordinates CPMS activities across assets, approves study designs and regulatory documents, and works with digital medicine, imaging, modelling and data science partners. Reports into the Respiratory, Immunology & Inflammation Research Unit.

AI/ML · Digital Medicine · Translational Imaging +3

• Stevenage
• Hybrid
• US$222,750 – US$371,250 pa
• Director

Leads end-to-end Model-Informed Drug Development and clinical pharmacology strategy across the drug development lifecycle, from first-in-human studies through filing and lifecycle management. Coordinates CPMS activities across assets, approves study designs and regulatory documents, and works with digital medicine, translational imaging and modelling specialists. Based in Stevenage with a planned relocation to Cambridge, UK by early 2029.

MIDD · QSP · AI/ML

• Portsmouth
• On-site
• Senior
• Permanent

Responsible for new product development and improvement projects for hardware and disposable devices used in the biotech industry, taking initiatives from spec definition through design, testing and validation to manufacturing transfer. Provides technical leadership on complex engineering challenges, applies 3D CAD design, manages project plans and resources, and reports progress to leadership. On-site role with up to 20% international travel.

• Newcastle upon Tyne
• Hybrid
• Director

Provides medical and clinical leadership for the development of novel diagnostic and companion diagnostic assays and platforms supporting precision medicine. Acts as subject matter expert for R&D projects, clinical studies and regulatory submissions, and supports pharma partnerships and pathology education. Hybrid role based in Newcastle Upon Tyne with 30-40% international travel.

IVD · CDx · Digital Pathology

• Livingston
• On-site
• Entry level

Assembles clinical trial test kits with specimen collection materials according to protocol, prepares investigator instruction manuals and flowcharts, and packages completed kits with documentation and ancillary supplies for shipment. Monitors inventory levels and alerts supervisors when supplies run low to prevent study delays. Site-based role requiring strong attention to detail and organizational skills.

• Reading
• Mid-level

Shapes and drives end-to-end clinical trial supply strategy, translating study protocols into kit designs, demand forecasts and packaging plans. Oversees vendors, IRT systems, distribution and temperature-excursion management while leading client and vendor meetings. Combines analytical planning with operational leadership across GxP-regulated clinical supply work.

Interactive Response Technology · Microsoft Word · Microsoft Excel +1

• Weston-super-Mare
• On-site
• £23 – £24 ph
• Senior
• Temporary

Support the daily operational management of a Clinical Chemistry laboratory, performing routine and specialist testing, result validation, and analyser maintenance. Work with Beckman Coulter DxC700 AU, DxI 800 and DxA Automation Track systems, Remisol middleware and WinPath LIMS, participating in IQC/EQA and ISO 15189 compliance.

Beckman Coulter DxC700 AU · Beckman Coulter DxI 800 · Beckman Coulter DxA Automation Track +2

• Herzliya, Israel
• Lead

Drive external deal flow by building relationships across innovation hubs, universities, venture capital and corporate venture groups, then match opportunities to internal capability gaps. Own end-to-end partnership management, from screening and diligence through negotiation, vendor onboarding and contracting, while providing outside-in analysis on investment memos and assessing technical novelty.

• London
• Hybrid
• Lead

Leads statistical work for post-marketing clinical trials, observational studies and real world data investigations, serving as Statistics lead on assigned projects. Develops protocols, analysis plans and TFL specifications, collaborating with clinical development, medical affairs, health economics and real world evidence teams. Requires strong SAS and R skills with a drug developer mindset.

SAS · R

• London
• £60,000 – £75,000 pa
• Senior · manages people

Lead the UK scientific affairs strategy for an international probiotic and functional food organisation, acting as senior scientific authority. Build KOL relationships across academia and healthcare, oversee human studies and research, ensure claims meet regulations, and manage a scientific affairs team while collaborating with European and global colleagues.

• Cardiff
• Entry level
• Permanent

Performing hair sample sectioning, preparing sample batches, and analysing laboratory samples for alcohol and drugs of abuse. Adhering to Standard Operating Procedures, completing documentation, and carrying out routine maintenance and calibration of laboratory equipment. Requires knowledge of ISO17025 and prior laboratory experience, with a degree in Biomedical Sciences, Biochemistry or a related discipline.

• London
• Hybrid
• Director · manages people

Leads the development and execution of international regulatory strategy across European and Rest of World markets, from first-in-human through post-marketing. Represents Global Regulatory Affairs on core development teams, manages project plans and resources, and advises senior management. Also a people manager within the International GRA leadership team, driving process improvement and regulatory policy engagement.

EMA

• Macclesfield
• On-site
• Senior
• Permanent

Designs and executes work plans for early drug discovery projects within a Protein Sciences team, supporting multiple projects and presenting results to clients. Hands-on role focused on recombinant protein expression using insect cell systems such as BEVS, S2 and Sf9, including construct design, baculovirus generation and troubleshooting difficult targets like membrane proteins.

BEVS · Sf9 · Sf21 +2

• United Kingdom
• Remote
• Mid-level · manages people

Lead statistician role delivering analysis database creation, statistical analyses, and formatted tables and summaries with minimal oversight, while mentoring junior team members. Involves leading project teams, interacting directly with sponsors, developing statistical analysis plans and randomization schemes, and programming or validating statistical tables with a strong emphasis on efficacy endpoints using SAS.

SAS · SAS BASE · SAS STAT +2

• Oxford
• On-site
• Director · manages people
• Permanent

Builds and leads a molecular biology and synthetic biology function within a plant science institute, setting technical strategy for high-throughput assays, sequencing-based readouts, CRISPR guide design and multiplex editing. Acts as a responsive core facility, coaching scientists on experimental design and integrating with bioinformatics, tissue culture and phenotyping teams. Combines deep technical direction with people leadership rather than routine bench work.

AI · Automation · Microfluidics +3