Biotechnology Jobs

• Zug, Switzerland
• Hybrid · 2 days in office
• US$266,250 – US$443,750 pa
• Director · manages people

Leads global development of an oncology medicine from clinical proof of concept to approval in first major markets, acting as single point of accountability. Builds and directs a matrixed Medicine Development Team spanning clinical, medical, commercial and manufacturing, driving strategy, governance and go/no-go decisions. Hybrid role with at least two days on-site.

• London
• Hybrid · 2 days in office
• US$266,250 – US$443,750 pa
• Director · manages people

Strategically leads global development of an oncology medicine from clinical Proof of Concept to approval in first major markets, acting as single point of accountability. Builds and leads a matrixed Medicine Development Team spanning clinical, medical, commercial and manufacturing, driving strategy, governance, budgets and lifecycle planning.

• Oxford
• On-site
• £40,000 pa
• Entry level
• Permanent

Designs and troubleshoots experiments in synthetic chromosome engineering, including centromere design, mitotic segregation and meiotic recombination in mammals and plants. Involves large DNA construct assembly, cell culture, NGS, live-cell imaging and FISH, plus computational analysis, publishing, mentoring junior researchers and pursuing IP and translational opportunities.

NGS

• Oxford
• On-site
• £40,000 pa
• Entry level

Develops generative protein design models that capture enzyme dynamics and function, designing conformationally dynamic catalysts. Runs computational and statistical analyses, publishes findings, and collaborates with in vivo evolution teams across the institute. Also mentors PhD students and research assistants and pursues translational and IP opportunities.

• Luton
• Hybrid · 3 days in office
• Senior

Lead UK direct tax compliance and reporting for a FTSE 100 biopharmaceutical group, preparing and reviewing corporation tax computations, patent box and capital allowance claims, and quarterly and year-end tax provisions. Advise the UK business on legislation changes, HMRC audits and governance regimes, while driving process efficiencies through automation and AI.

• London
• Hybrid
• £63,917 – £118,703 pa
• Director

Acts as a QA liaison between clinical trial teams and third parties, providing expert support through due diligence, qualification, governance and ongoing monitoring. Focuses on technology-enabled vendors such as digital health tools, medical devices and AI, covering risk assessment, audit support, inspection readiness and escalation of quality issues.

DHT · SaMD · SaaS +1

• Cambridge
• On-site
• £20 – £24 ph
• Mid-level
• Temporary

Undertake routine and specialist microbiological and molecular investigations across bacteriology, Containment Level 3, serology, chlamydia and molecular diagnostics, interpreting and reporting results. Operate and maintain automated analysers, manage consumables and lab IT systems, and contribute to quality management, audits and SOP development. Based at Addenbrooke's Hospital within UKHSA's Public Health Microbiology team.

UKAS · HSE

• Harrogate
• Entry level

Trainee role performing routine macroscopic necropsy techniques, trimming and retaining organs across a wide range of species. Involves animal handling and euthanasia, precise sample labelling, data recording and reagent preparation, with training provided and some out-of-hours and weekend cover expected once trained.

• Harrogate
• On-site

Coordinate genetic toxicology studies alongside Study Directors, handling day-to-day study tasks, drafting protocols and amendments, scheduling sample shipments, and preparing study reports. Requires GLP knowledge and technical writing within a scientific setting, managing multiple changing priorities in an office-based team.

• Leeds
• Hybrid · 3 days in office
• Entry level
• Permanent

Develops protocols and clinical study reports for early-phase trials (I-IIa), focusing on safety and pharmacokinetics. Coordinates cross-functional teams and client stakeholders to drive documents from draft to final deliverable, with on-the-job training in medical writing.

• 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

• High Wycombe
• Entry level
• Internship

Supports the Local Trial Manager and Site Manager with document management and administrative tasks across trial start-up, execution and close-out, ensuring compliance with SOPs and local regulatory requirements. Also contributes to process improvement, training and mentoring of other CTAs, partnering with Business Operations, study teams and stakeholders such as Finance and Procurement.

Microsoft Word · Microsoft PowerPoint · Microsoft Excel

• London
• Hybrid
• Senior
• Permanent

Acts as subject-matter expert for the organisation's ELN platform, owning its configuration, governance and continuous improvement across R&D laboratories. Builds workflows, templates and integrations, supports superusers, and leads development of a centralised Technical Development data repository using SQL and analytics to enable data-driven scientific decisions.

Benchling · JMP · APIs

• Cambridge
• Hybrid · 3 days in office
• Director

Leads an integrated Business Continuity and Crisis Management capability across Oncology R&D, owning the framework, risk registers and BIAs while designing executive-level crisis exercises. Drives emerging-risk assessment, supply-chain nth-tier visibility and the practical use of AI in resilience practice, acting as the audit and regulatory interface for standards such as NIS2.

NIS2 · Business Continuity Software

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

Owns Evotec's in silico therapeutics design capability, uniting computational chemistry, generative and modality design (small molecules, peptides, protein engineering, degraders, molecular glues) and predictive ADMET/safety under one mandate. A newly created unit within the In Silico & AI group with an explicit build mandate: set technical vision, grow a multi-site team, and industrialise repeatable, benchmarked methods across partner programmes.

RDKit · Python · AlphaFold