Biotechnology Jobs

CureAge Therapeutics · London

Lead the computationally guided design of a lipid nanoparticle delivery platform, applying chemical and biophysical principles to optimise LNP composition and formulation. Use AI-enabled chemistry, cheminformatics, predictive models and molecular modelling to prioritise formulation components, working closely with the experimental team and founding team in a small start-up.

Lypo · Edinburgh · £31,000 – £36,000 pa

Implement high-throughput plasmid assembly, colony PCR, Minipreps and pathway construction to build strains for hypothesis testing and model training. Work across disciplines in a lab-based, cross-pollinating team, with fortnightly research updates, mentorship and organised labbook/data keeping. Golden Gate assembly, Benchling in silico cloning and DNA sequencing are core.

Danaher · Portsmouth

Graduate programme within a filtration R&D team, supporting development of liquid and air filtration technologies for pharmaceutical and biotech manufacturing. Involves designing and analysing lab experiments, product testing, data interpretation and reporting, working from concept through validation to manufacturing. Structured training, mentoring and cross-functional exposure in a regulated industry.

Aarhus University · Aarhus, Denmark

A PhD fellowship combining field sampling at Danish biogas plants with laboratory work and computational analysis. The candidate will use PCR/RT-qPCR surveillance, long-read shotgun metagenomics, culture and viability methods to trace microbial transmission from imported biomass through hygienisation barriers, plus controlled experiments on persistence and inactivation.

Eurofins · Liverpool

Perform routine, non-routine and stability testing on finished pharmaceutical products at a client site, using HPLC, Dissolution, Karl Fischer and UV techniques. The role also covers technology transfers, analytical validation, GMP data review and OOS investigations, working within a managed services team embedded at the client's facility.

Danaher · Newcastle upon Tyne

Graduate-level role in a cancer diagnostics R&D team, generating and evaluating antibodies and detection methods for in vitro diagnostic assays on manual and automated staining systems. Involves laboratory work, literature and competitor reviews, and contributing to product development, verification and validation in a regulated environment, with training in histopathology and immunohistochemistry.

Queen's University Belfast · Belfast · £35,000 – £37,532 pa

A graduate-level KTP Associate role based at Norbrook Laboratories, working within the R&D team to develop a data-driven framework for pharmaceutical scale-up of liquid dosage veterinary medicines. The project focuses on predictive modelling of process parameters and product quality across scales, combining chemical engineering principles with statistical and hybrid data modelling, delivered in collaboration with Queen's University Belfast's School of Pharmacy.

Eurofins · Liverpool

Perform method development and proof-of-concept validation on pharmaceutical raw materials, intermediates and drug substances, mainly APIs, using HPLC, GC and MS. Support technology transfers for novel substances, review data for compliance, investigate OOS/OOE results and document work to client procedures. Based on-site at a client facility as a managed PSS scientist, liaising with client representatives and supporting audits and continuous improvement.

Bond Williams · London · £40,000 – £50,000 pa

Hands-on lab role expressing and purifying recombinant proteins using bacterial, cell-free and other systems, plus preparing buffers and reagents to precise specs. You'll run QC and release testing (SDS-PAGE, purity, activity assays), maintain batch records in an eQMS, write SOPs and support deviations and CAPAs while optimising and scaling production processes.

GSK · London

Lead statistical planning and delivery across oncology clinical programs, designing trials and analyses that shape development and regulatory strategy. Work with clinical, regulatory, safety, data science and commercial teams, using Bayesian methods and simulation in R or Python, while mentoring statisticians.

University of Cambridge · Cambridge · £38,448 – £46,970 pa

Primarily experimental wet-lab postdoc developing programmable nucleic-acid systems that sense defined human genomic sequences and convert molecular recognition into engineered DNA outputs, with applications to genetic privacy. Based in the Department of Genetics, the role involves hands-on design, construction and troubleshooting of novel molecular systems plus quantitative analysis of assay performance to guide experimental iterations.

GSK · USA - Pennsylvania - Upper Providence

Lead statistical planning and delivery across oncology clinical programs, designing trials and analyses that shape development and regulatory strategy. Work with clinical, regulatory, safety, data science and commercial teams, applying Bayesian methods, simulations and advanced modelling in R or Python, while mentoring statisticians.

Animal & Plant Health Agency · Addlestone · £40,056 pa

Design and execute scientific investigations into mammalian viral pathogenesis and host-pathogen interactions, ensuring work meets ISO9001, budget and customer requirements. Communicate findings via conferences and peer-reviewed journals, supervise staff and students, and pursue national and international research funding. Includes rostered on-call cover for weekend and Bank Holiday diagnostics.

Johnson & Johnson Innovative Medicine · High Wycombe

A 12-week summer internship in EMEA Global Regulatory Affairs within the Oncology therapeutic area, working on a hybrid model with three days on site. Interns join a global matrixed team supporting clinical strategies and Phase I-III oncology studies, contributing to regulatory strategy, clinical trial applications and product registration activities, with a mentor, cross-functional team meetings and a research poster presented at a company-wide symposium.

Pfizer · United Kingdom - Walton Oaks

Conduct strategic regulatory activities for assigned products and markets, managing Marketing Authorisation applications, variations, renewals and NRA queries. Work with cross-functional teams and above-country hubs to maintain compliance, support clinical trial applications and share regulatory intelligence.

Roche · Welwyn

Provides safety science and pharmacovigilance support across the Roche portfolio, covering signal detection, benefit-risk assessment, ICSR case management and aggregate reporting such as DSUR and PBRER. The role also involves preparing CCDS, labelling, RMP and REMS documents and shaping drug safety input into clinical development strategy. Level is set by experience, working with a global team from the Welwyn office.

Russell Taylor Group · Deeside · £29,000 – £34,000 pa

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.