Biotechnology Jobs

• Macclesfield
• On-site
• Senior
• Permanent

Perform routine and non-routine analytical testing of pharmaceutical oral drug products and new modalities using HPLC, Karl Fischer, dissolution and mass spectrometry. Review data for GLS and GMP compliance, investigate out-of-specification results, and develop, optimise and validate analytical methods while training colleagues and driving continuous improvement at a client's Macclesfield facility.

HPLC · Karl Fischer · Mass Spectrometry +1

• Macclesfield
• On-site
• Mid-level
• Permanent

Perform routine and non-routine analytical testing of pharmaceutical oral drug products and new modalities using HPLC, Karl Fischer, dissolution and mass spectrometry. Review data for GLS and GMP compliance, investigate out-of-specification results, and develop and validate analytical methods while training colleagues and supporting client projects at a Macclesfield pharma facility.

HPLC · Karl Fischer · Mass Spectrometry +1

• Oxford
• On-site
• Senior · manages people

Lead development, qualification, validation and execution of complex cell-based immunoassays generating clinical trial data across therapeutic areas. Act as scientific point of contact within the Immuno-assays group, performing GCP/GLP-compliant sample testing, authoring validation reports, and mentoring junior lab staff. Fully onsite at Harwell, reporting to the Associate Director, Immuno-assay UK.

GraphPad Prism · Microsoft Word · Microsoft Excel +2

• Deeside
• On-site
• £29,000 – £34,000 pa
• Mid-level

Hands-on laboratory role supporting diagnostic testing, assay development and IVD kit manufacture, including formulation, PCR and capillary sequencing. Duties cover sample processing, quality control of materials and finished products, stability storage, data analysis and GDP-compliant record-keeping, with project ownership and possible training or supervisory support.

PCR · Capillary Sequencing

• Edinburgh
• Lead

Designs, delivers and interprets complex molecular and cellular biology studies for drug discovery and translational research, combining hands-on lab work with technical direction across client programmes. Provides scientific leadership on multiple projects, evaluates new technologies and supports colleagues, working with mammalian cell cultures and advanced cellular systems.

• Stevenage
• Lead

Leads digital use cases across the CMC portfolio, translating analytical workflows and user needs into business requirements, success criteria and deployed digital solutions. Runs cross-functional teams end to end from concept to go-live, covering business acceptance testing, change management, training and adoption. Sits at the intersection of science, process and technology within GSK's CMC Digitalisation transformation.

Artificial Intelligence · Laboratory Informatics

• Livingston
• Mid-level

Leads strategic sourcing of animal models, especially rodents and genetically engineered strains, for an early-phase discovery business. Manages supplier relationships, RFIs/RFPs, contract negotiations and performance reviews, while partnering with scientific, veterinary and quality teams on capacity planning, welfare and regulatory compliance.

• Cambridge
• Senior

Introduction to role:The Senior Scientist – Upstream Process Development position is a temporary maternity-cover role responsible for the hands-on scientific and technical delivery of upstream mammalian cell culture process development activities supporting AstraZeneca’s biologics pipeline. Working under minimal supervision, the…

• Saffron Walden
• Hybrid
• £3,452 – £3,861 pm
• Contract

Develops and maintains Python and Java data pipelines that generate ChEMBL releases, plus other chemogenomics services like SureChEMBL, UniChem and ChEBI. Involves database administration, integrating external chemical databases, and collaborating with interdisciplinary scientists and engineers on curation and quality issues.

RDKit · Open Babel · InChI +7

• Keele
• £39,560 – £48,337 pa
• Entry level
• Contract

A postdoctoral research associate role delivering the insect-focused laboratory components of a consortium project on a planthopper-vectored bacterial plant disease. The postholder investigates vector ecology and transmission biology using insect rearing, bioassays, EPG analysis and molecular techniques such as PCR and qRT-PCR, with occasional travel within the UK and Europe.

Electrical Penetration Graph · Bioinformatics

• Sheffield
• £39,560 – £41,885 pa
• Entry level
• Contract

Contribute to a research programme analysing explanted polymeric medical devices, investigating how implant degradation, tissue responses and patient-specific factors drive complications. Establish experimental and sample-handling workflows, develop lab methods to characterise tissue and immune responses, and collaborate with academic, clinical, regulatory and patient partners including Sheffield Teaching Hospitals and Cambridge.

• Leeds
• Director · manages people

Owns product strategy, roadmap and innovation for clinical pharmacology clinics and bioanalytical labs, spanning early-phase platforms like ClinSpark, LIMS/LIS, ELN, instrument connectivity and lab automation. Builds business cases and secures funding, governs a regulated portfolio, and leads multidisciplinary product teams and vendors across distributed sites.

ClinSpark · LIMS · LIS +7

• Oxford
• On-site
• £39,424 – £43,984 pa
• Entry level
• Contract

Carries out laboratory research on synthetic genome DNA assembly, generating constructs and testing new approaches using recombinant DNA methylases. Involves molecular cloning, long DNA molecule extraction, bacterial culture and recombinant protein production and purification, with scope for some bioinformatic analysis. Based in a well-equipped Oxford lab, collaborating on translation of synthetic chloroplast genomes into crop plants such as potato and wheat.

DNA Methylases

• Oxford
• Hybrid · 3–4 days in office
• Director

As an individual contributor in the Clinical Pharmacology group, you will develop quantitative strategies for dose selection, PK/PD characterization and regimen optimization across oncology, immunology and rare disease programs. You will partner with Pharmacometrics and QSP colleagues, represent CQP on program teams, and contribute to regulatory documentation and interactions.

R · Phoenix WinNonlin · NONMEM +2

• London
• On-site
• Mid-level

Develops and optimises therapeutic delivery formulations, designing lab experiments to assess stability, physicochemical properties and in vitro performance. Works in a multidisciplinary biotech team, characterising formulations analytically and supporting scale-up and tech transfer towards manufacturing. Distinct for its blend of formulation science, experimental development and translational research.