Biotechnology Jobs

• 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

• Cambridge
• Senior

Leads stem cell-focused drug discovery projects, designing and optimising human iPSC-derived models, 2D/3D assays and disease models, and applying New Approach Methodologies to client programmes. Partners directly with pharmaceutical and biotech clients, presenting data and shaping project strategy, while mentoring colleagues and contributing to proposals and capability development.

Organoids · Spheroid systems · Co-culture models +4

• Opfikon, Switzerland
• Hybrid · 3 days in office
• US$317,000 – US$409,000 pa
• Director · manages people

Leads the cross-functional Clinical Development Team as lead scientific expert, owning the Clinical Development Plan and integrating internal and external contributions into program strategy. Serves as medical monitor, authors key regulatory and study documents, and presents to safety and review committees.

• Maidenhead
• Senior

Acts as case management subject matter expert for assigned clinical trials, overseeing safety reporting plans, vendor performance and ICSR compliance. Leads pharmacovigilance processes, supports GxP inspections and audits, and provides study-specific training to vendors and internal teams. Requires deep PV and regulatory knowledge in a multinational pharmaceutical setting.

Drug Safety Database

• London
• Hybrid · 3 days in office
• Lead

Owns safety assessment strategy for drug discovery projects from inception to regulatory submission, working with small molecule and biologics platforms. Designs screening cascades, authors IND packages, and manages CRO relationships for outsourced wet-lab work. Also guides development of an AI predictive toxicology platform with ML researchers.

AI/ML · AlphaFold

• Warsaw, Poland
• Hybrid
• PLN 318,000 – PLN 530,000 pa
• Director

Leads signal detection and evaluation for assigned products, prepares global regulatory reports and risk management plans, and supports safety governance meetings across clinical and post-marketing settings. Works in cross-functional matrix teams, contributes to risk-reduction strategies, and mentors colleagues while driving process improvements in pharmacovigilance.

Safety Databases · Data Visualisation Tools

• London
• Hybrid
• £67,900 – £126,100 pa
• Senior

Lead the authoring of high-complexity regulatory documents and act as Program Writer for complex programmes, overseeing writing strategy, coordination, planning and resourcing. Partner with clinical trial and submission teams, shape data analysis planning, and champion AI tools to improve regulatory writing quality and efficiency.

Artificial Intelligence

• London
• Hybrid
• £49,140 – £91,260 pa

Author and manage high-quality regulatory documents for clinical and submission teams, advising on writing standards and best practices. Collaborate cross-functionally on data analysis planning and presentation, lead writing plans and timelines, and apply AI tools to improve efficiency. Requires strong biostatistics understanding and pharmaceutical industry experience.

Artificial Intelligence

• Stevenage
• Hybrid · 2–3 days in office
• US$151,500 – US$252,500 pa
• Director

Leads cross-functional project teams within Oncology Translational Medicine to progress diagnostic and biomarker development activities, coordinating with clinical, regulatory, quality, finance and external lab partners. Builds integrated timelines, tracks budgets, milestones and contracts, mitigates risks, and supports regulatory submissions and technical evaluations of diagnostic technologies.

Microsoft Project · Microsoft Word · Microsoft Excel +7

• London
• Hybrid · 3 days in office
• Lead

Lead formulation strategy for small molecules across drug discovery and preclinical development, designing technologies such as solid dispersions and co-crystals to improve solubility, stability and manufacturability. Work within an interdisciplinary team alongside AI/ML drug design platform groups, managing external CRO resources and authoring regulatory submissions.

ASAP

• Remote Opportunity - United States
• Remote
• US$261,800 – US$346,060 pa
• Director

Lead clinical pharmacology and pharmacometrics strategy across a portfolio of rare disease and oncology programs, serving as the clinical pharmacology lead and regulatory representative. Oversee modeling and simulation (population PK, PK-PD, exposure-response) and provide pharmacology input on Phase 1-3 study designs. Work cross-functionally with clinical, translational and discovery teams in an end-to-end drug development environment.

WinNonlin · Monolix · NONMEM +1

• Macclesfield
• Permanent

Provide analytical support for drug substance manufacturing and method development, running project analysis, forced degradation studies and proof-of-concept validation. Author and review Analytical Testing Plans, method protocols and validation protocols, using HPLC and GC within a GMP-regulated lab. Work independently and in a multidisciplinary team, communicating findings to internal and external stakeholders.

HPLC · GC · NMR +4

• Oxford
• On-site
• Mid-level
• Temporary

Hands-on individual contributor role operating production equipment for mRNA vaccine manufacturing at the Harwell site, following cGMP, SOPs and safety requirements. Involves troubleshooting equipment and digital issues, basic maintenance, documentation with Quality Assurance, and RCA/CAPA investigations, with exposure to continuous improvement and Generative AI tools.

Generative AI

• Leeds
• On-site
• Entry level
• Permanent

Prepare and handle investigational medicinal products in a cGMP clean room, applying sterile technique and GMP during live first-in-human studies. Work in pairs with Technical Officers on study set-up, dose calculations, batch records and equipment checks, with the clinic and pharmacy under one roof at an MHRA-accredited Phase I unit.

Outlook · Word · Excel +1

• Leeds
• On-site
• Senior

Lead early-phase clinical trials as Principal Investigator or Project Physician, taking studies from start-up through closeout and the Clinical Study Report. Work across first-in-human studies, multiple therapeutic areas and an NHS Trust collaboration, with on-call cover and mentoring of less experienced physicians.

MHRA · cGMP · NHS Trust