Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$242,250 – US$403,750 pa
• Director · manages people

Owns the clinical strategy, scientific narrative and benefit-risk framework for genitourinary cancer assets, acting as the senior clinical authority on the Medicine Development Team core quad. Sets asset-level evidence-generation and governance direction while Senior Scientists handle study-level delivery, and represents Clinical Development in health authority and external engagements. Hybrid role with at least two on-site days per week.

AI · Advanced Analytics

• Stevenage
• Lead

Develops and deploys cheminformatics and machine learning models on large proprietary datasets to guide go/no-go decisions across drug-discovery programmes. Embeds predictive models into multidisciplinary teams spanning DMPK, toxicology and safety pharmacology, and prototypes LLM-driven agent workflows for design-make-test-analyse cycles.

ChemAxon · RDKit · Pipeline Pilot +2

• Oxford
• On-site
• Senior

Provides hands-on MS&T engineering expertise across drug substance manufacturing and label, packaging and final-storage operations at the Harwell site. Leads technology transfer, process start-up, validation, continued process verification and troubleshooting, authoring protocols and reports as an individual contributor. Works cross-functionally with Manufacturing, Quality and Supply Chain, with on-call or shift coverage as required.

SAP · VEEVA · DeltaV +4

• Oxford
• On-site
• Senior

Hands-on maintenance of GMP manufacturing equipment at a new mRNA vaccine facility, including autoclaves, filling lines, isolators, TFF systems and chromatography skids. Acts as first responder to equipment failures, performing structured root-cause troubleshooting, preventative maintenance, CAPA work and cGMP documentation, while coordinating vendors and contractors. Includes on-call rotation for 24/7 operations and OJT delivery.

Excel · Word · PowerPoint +1

• Milton Keynes
• Remote
• £37,500 pa
• Mid-level
• Permanent

Provide first-line remote technical support for specialist laboratory analysers and medical devices, diagnosing faults using remote-access tools such as RDP, VNC and augmented reality. Work with laboratory staff, field service engineers and product specialists to resolve issues and minimise on-site visits, while training users and maintaining service records.

RDP · VNC · Augmented Reality

• London
• Hybrid
• Lead · manages people

Leads one or more Early Development Asset Teams, owning integrated strategy from candidate nomination through first-in-human trials across preclinical, translational, clinical, regulatory and CMC workstreams. Serves as scientific champion for oncology assets, presenting data and investment recommendations to governance bodies and contributing to in-licensing due diligence.

• Abingdon
• Director · manages people
• Permanent

Leads Evotec's consolidated AI Accelerator, owning machine learning, generative and agentic AI, and therapeutic hypothesis groups. Sets the AI vision and roadmap, makes build/buy/partner decisions for the AI stack, and turns proprietary multi-omics and experimental data into predictive models and reusable IP. Acts as the senior external technical voice for AI in drug discovery.

• Abingdon
• Lead
• Permanent

Acts as the single front door between Evotec's Drug Discovery Platforms and the global In Silico & AI organisation, owning demand, relationships and the in silico roadmap. Translates platform science needs across DMPK, ADME/Tox, predictive safety, screening and omics into prioritised AI requirements, then orchestrates delivery across capability units. Carries a commercial mandate, contributing to client proposals, pricing and evidencing value such as margin uplift and cycle time.

• Livingston
• Mid-level · manages people

Supervises a team of laboratory staff in a central laboratory services environment, setting day-to-day operational activities and ensuring effective delivery. Oversees hiring, training, performance management, safety compliance, CAPA and quality incident resolution, and reviews laboratory metrics to drive process improvement. Requires immunology-based clinical laboratory or clinical trials experience and proficiency with LIMS.

LIMS

• Bedford
• On-site
• £41,832 pa
• Mid-level · manages people

Hands-on leadership of a pharmaceutical warehouse shift, overseeing receipt, storage and dispatch of chilled and controlled drugs while managing and developing a team. Ensures MHRA compliance through audits, root cause analysis and CAPAs, plus health and safety, budget monitoring and continuous improvement of workflows.

WMS · Six Sigma

• London
• Hybrid
• Senior

Oversees quality control testing for a genetically edited cell therapy, acting as lead point of contact for external CDMOs and QC labs on GMP release, stability and method lifecycle work. Leads OOS/OOT investigations, reference standards and assay controls programmes, authoring and approving SOPs, COAs and protocols. Hybrid role based in London requiring close collaboration with contract test labs and management on compliance risks.

LIMS

• Maidenhead
• Hybrid
• Senior · manages people
• Permanent

Technical lead for all data management activities on late phase (IIb-III) clinical trials, from start-up through completion. Develops Data Management and Quality Management Plans, designs CRF/eCRF and database structures, and coordinates edit checks and discrepancy management. Acts as client liaison, tracking cycle times and metrics while overseeing data review staff.

RAVE · EDC

• Harrow
• Remote
• Senior

Acts as principal labelling strategist within Global Regulatory Affairs, driving development and maintenance of dCCDS, CCDS, USPI and EU SmPC documents across an assigned product portfolio. Leads Global Labeling Committee reviews of proposed label exceptions and represents labelling on regulatory strategy teams, working with safety, clinical and commercial stakeholders. Home or office based across European locations.

Company Core Data Sheet (CCDS) · Development Company Core Data Sheet (dCCDS) · US Prescribing Information (USPI) +3

• London
• Hybrid
• Director
• Permanent

Lead clinical pharmacology and pharmacometrics across a growing drug discovery portfolio, serving as the quantitative lead on cross-functional project teams. Apply MIDD, PBPK, population PK/PD and QSP modelling to translate nonclinical data into human dosing and trial design, spanning small molecules, biologics and novel platforms. Also manages CRO partnerships and authors regulatory submissions.

NONMEM · R · Monolix +3

• Ireland

Regional Laboratory Manager – DublinRandox are a world leader in diagnostics for clinical healthcare, toxicology, and food security. Our expertise and product portfolio have assisted laboratories across the world in improving health and saving lives. Our global success is a…