Biotechnology Jobs

• Cambridge
• Lead · manages people

Lead scientific strategy for cardiac electrophysiology and translational ion channel research, acting as scientific lead across multiple integrated drug discovery programmes. Guide experimental design using automated patch clamp (Qube/Sophion), MEA systems and hIPSC-derived cardiomyocytes, while serving as primary client contact and mentoring scientists.

Qube · MEA Systems · Sophion

• London
• On-site
• Lead · manages people
• Permanent

Owns the end-to-end sample-to-sequence pipeline for the Trillion Gene Atlas, spanning DNA extraction, library prep and sequencing dispatch across Phase 1 and Phase 2. Bridges R&D and production by scaling validated protocols, applying Lean/Six Sigma to improve throughput, and leading a small lab team while monitoring data return with bioinformatics partners.

Illumina · Ultima · PacBio +3

• Wrexham
• Director · manages people

Leads Ipsen's global Biologics Process Development organisation, owning CMC drug substance strategy for toxins, monoclonal antibodies, ADCs and enzymes from candidate selection through launch and lifecycle. Manages process and analytical development teams, acts as CMC sponsor, and directs CDMO partnerships, tech transfer and regulatory submissions. Also serves as PharmDev/R&D site lead in Wrexham on the cross-divisional Site Leadership Team.

CDMOs

• 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…

• London
• Hybrid · 2–3 days in office
• Junior

Contribute across a full-stack cloud product and IoT devices that interface with hardware automating human cell production. Work spans TypeScript, React, GraphQL frontends and Node.js/PostgreSQL backends, with cross-disciplinary collaboration alongside hardware engineers and biologists, including testing on prototype machines in the lab.

React · TypeScript · GraphQL +7

• United Kingdom
• Remote
• Senior

Clinical Research Associate role within PPD's Functional Service Provider division, dedicated to a client and embedded in multi-national project teams. You perform and coordinate all aspects of clinical monitoring, conducting monitoring activities independently across challenging projects. Requires ICH-GCP, EU and FDA knowledge, with award-winning training provided.

• Didcot
• On-site
• Lead · manages people

Lead a team of software engineers delivering next-generation Raman spectroscopy software from the Laser Spectroscopy Center of Excellence in Oxford (Harwell). The role owns R&D operations across the software product lifecycle, solving engineering challenges and integrating hardware and software with global partners, using modern architectures such as containerisation, Kubernetes, microservices and cloud deployment.

Kubernetes · Linux · Microsoft

• London
• Senior

Advise clients on complex biotechnology and life sciences patent matters, with a focus on contentious work including UPC proceedings and international patent litigation. The firm handles more than 30 UPC cases and offers a structured programme supporting progression towards Partnership, with mentoring of junior colleagues also expected.

UPC

• London
• Hybrid · 3 days in office
• Director · manages people

Lead all externalised drug discovery and preclinical lab operations, building and scaling a global CRO infrastructure for an AI-first drug design platform. Oversee experimental throughput, data QC and turnaround times, embed data-generation-by-design standards, and manage vendor governance, budgets and a team of CRO Scientific Leads, Operations Managers and Compound Managers.

AlphaFold · Agentic AI

• London
• Hybrid · 3 days in office
• Senior

Lead translational pharmacology for an AI-first drug discovery team, shaping neurodegeneration strategy and target validation. Bridge dry-lab predictive models with experimental biology, designing screening cascades and profiling AI-designed molecules. Manage CRO partnerships and serve as scientific lead for portfolio programs.

SPR · TR-FRET · Mass Spectrometry

• London
• Remote
• Senior

Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review while managing risk-based quality and regulatory compliance. Works within a local study team supporting a key sponsor, with travel across the UK and internationally.

CTMS · eTMF

• London
• Remote
• Senior

Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review. Works within a local study team for a key sponsor, using CTMS, eTMF and risk-based quality management, with travel across the UK and internationally.

CTMS · eTMF

• United Kingdom - Walton Oaks
• Hybrid

Lead and implement regional regulatory strategies for assigned products, acting as the regional representative within Pfizer's Global Regulatory Strategic Team. Accountable for timely submissions, approvals and optimal interactions with Health Authorities, partnering cross-functionally to align regulatory plans with commercial goals.

ChatGPT · Microsoft Copilot

• United Kingdom
• Remote
• Director · manages people

Senior medical leadership role within a clinical research organisation, acting as a cardiovascular subject matter expert supporting proposals, bid defences and client engagement. Responsibilities span RFP input, protocol and regulatory strategy, internal therapeutic training, and mentoring clinical scientists, with peer-level interaction with pharma medical leadership.

PPD

• United Kingdom
• Remote
• Mid-level

Independently manages basic project tasks including budgets, timelines and client correspondence, while supporting protocol and report development under senior supervision. Conducts qualitative data collection such as cognitive interviews and focus groups, performs literature reviews and data analysis, and assists with scientific publications. Requires 10-30% travel and works within a multidisciplinary patient-centered research team.

Microsoft Word · PowerPoint · Excel +5