Biotechnology Jobs

• Barnard Castle
• Contract

Support a secondary manufacturing site's production area with technical services including new product introduction, troubleshooting, and technical projects. Design and validate manufacturing processes, drive improvements using lean and Six Sigma, and lead FMEAs, risk assessments and change controls under cGMP and EHS standards.

• Waltham, United States
• On-site
• US$150,975 – US$251,625 pa
• Mid-level

Key member of the Clinical Development team contributing to the design, execution, analysis and reporting of clinical studies across all phases. Works cross-functionally with Medical Monitoring, Clinical Operations, Biostatistics, Data Management and Regulatory Affairs, reviewing safety, efficacy, biomarker and PK/PD data and supporting CSRs and regulatory submissions. Based on-site in Waltham, MA or London, UK.

• United Kingdom

Field-based role maintaining and repairing Roche diagnostic systems across molecular, tissue and serum work areas, using on-site support and remote diagnostics to resolve complex electro-mechanical faults. Responsibilities include preventive maintenance, reporting, customer technical training and regulatory documentation, covering Exeter to Kent or a designated customer base.

Roche Diagnostics Systems · Remote Diagnostic Tools · Digital Portfolio

• United Kingdom

Field-based role maintaining and repairing Roche diagnostic systems across molecular, tissue and serum work areas, using on-site and remote diagnostics to resolve complex electro-mechanical faults. Involves preventive maintenance, reporting, customer technical training and regulatory documentation, working within a UK customer-centric field support team.

Roche Diagnostics Systems · Remote Diagnostic Tools · Digital Portfolio

• Field Force (England / Wales)
• Hybrid
• £32,690 – £60,710 pa

Site-facing role managing Phase I–IV clinical trial sites, acting as the primary contact between the sponsor and sites. Responsibilities include site initiation visits, training, on-site and remote monitoring, risk assessment and mitigation, and closeout activities, working closely with cross-functional teams to ensure data integrity and compliance.

• Macclesfield
• On-site
• Mid-level
• 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 and validate analytical methods while training colleagues and supporting client projects at a Macclesfield pharma facility.

HPLC · Karl Fischer · Mass Spectrometry +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

• Manchester
• Mid-level

Monitors Phase 3b and Phase 4 clinical trial sites across the UK and Ireland, performing selection, initiation, monitoring and close-out visits at a pace of six to seven per month. Tracks recruitment, regulatory submissions, CRF completion and data queries while ensuring GCP and ICH compliance and maintaining TMF and ISF documentation.

• Reading
• Mid-level

Monitors Phase 3b and Phase 4 clinical trial sites across the UK and Ireland, performing selection, initiation, monitoring and close-out visits at a pace of 6-7 visits per month. The role involves driving subject recruitment, delivering protocol training, tracking regulatory submissions and CRF data, and maintaining Trial Master File documentation in line with GCP and ICH guidelines.

• Uxbridge
• Hybrid
• Director

As a member of cross-functional development teams, you will contribute to trial design, protocol development, analysis planning, and regulatory submissions, with the option to support a specific asset indication. The role involves authoring statistical analysis plans and clinical study reports, defending protocols at governance reviews, and providing statistical leadership on health authority requests. It requires 50% onsite presence in Uxbridge and proficiency in SAS, R, or Python.

SAS · R · Python

• Saffron Walden
• Hybrid
• £3,452 – £3,861 pm
• Contract

Curate molecular interaction and macromolecular complex data from scientific literature and user depositions into the IntAct and Complex Portal knowledgebases. Work with bioinformaticians and developers to build curation workflows combining expert manual curation with AI-assisted literature mining, using ontologies and community data standards.

IntAct · Complex Portal · Gene Ontology +2

• London
• On-site
• Director
• Permanent

Leads CMC regulatory strategy for global submissions including IND, CTA, BLA and MAA, and oversees agency correspondence and compliance for mRNA products. Reviews submissions for readiness, drives health authority interactions, and advises manufacturing and quality teams on change controls and regulatory guidance across vaccines, oncology and rare disease programmes.

IND · CTA · BLA +1

• Taunton
• On-site
• £49,387 – £56,515 pa
• Lead · manages people
• Permanent

Lead a team of Biomedical Scientists and support staff across Bacteriology, Parasitology, Virology, Molecular and Mycology, rotating through all areas. Responsibilities include training, appraisals, quality management, policy development, clinical trials and senior management on-call, with lone working on evening and weekend shifts.

LIMS · Q-Pulse · Kiestra

• Macclesfield
• Senior

Laboratory-based role developing and scaling up bioconjugation of small molecules to antibodies and scaffolds, plus high-throughput workflows using liquid handlers. You'll characterise proteins and conjugates by HPLC, LCMS, UV/Vis and preparative chromatography (AKTA, TFF), interpret data and report to stakeholders in early-phase oncology drug discovery.

AKTA · TFF · Liquid Handlers +1

• Leeds
• Director · manages people

Leads technology product management for clinical pharmacology units and laboratories, owning strategy, roadmap and investment for clinic and lab platforms. Drives automation, AI, instrument connectivity and lab robotics across regulated GLP/GCP environments, from business case and funding through validation and adoption. Partners with scientific, quality and Clinical Operations leaders on shared capabilities and data.

ClinSpark · LIMS · LIS +7