Biotechnology Jobs

• Stevenage
• Hybrid
• Lead

Owns operational delivery of diagnostics across early and late-stage oncology trials, covering biosample collection, processing and storage, and implementation of clinical trial assays at reference and central labs and CROs. Works in a matrix with biomarker, clinical operations, data management, regulatory and procurement colleagues, managing vendors, contracts and data transfer agreements while keeping studies audit-ready.

• Waltham, United States
• Hybrid
• US$123,000 – US$205,000 pa
• Lead

Owns operational delivery of diagnostics across early and late-stage oncology trials, from biosample collection and clinical trial assays at reference and central labs to audit-ready data. Works in a matrix with Diagnostic Strategy, Biomarker, Clinical Operations, Data Management, Regulatory, Quality and Procurement, plus external CROs, labs and vendors, and mentors colleagues as a subject matter expert.

CRO

• 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

• Barnard Castle
• On-site
• Shift work

Carries out planned preventative maintenance, fault finding and repairs on manufacturing, packaging and utility equipment in a sterile pharmaceutical plant, responding to breakdowns to minimise downtime. Works within a shift-based cross-functional team, using SAP CMMS and GMP documentation, and supports root cause investigations, CAPAs and continuous improvement.

SAP · CMMS

• Ware
• On-site
• Mid-level

Ensures manufacturing and warehouse operations comply with SOPs, cGMP and UK/EU regulatory requirements, investigating deviations and managing CAPA, complaints and change control. Provides quality oversight of facilities, equipment and personnel, coaching staff and running GEMBA and process confirmation activities at a respiratory inhaler and oral solid dose site.

• London
• Director

Provides scientific and medical expertise at study level across early- and late-phase hepatology assets, serving as medical monitor for Phase 1–4 trials and leading protocol, IB, ICF and CSR authoring. Works within cross-functional global study teams and the Clinical Matrix Team, integrating efficacy, safety and biomarker data to inform asset and portfolio decisions, with informal coaching of less experienced clinical scientists.

• Stevenage
• Director

Provides scientific and medical expertise at study level across early- and late-phase hepatology assets, leading protocol and study document development, serving as medical monitor for Phase 1-4 trials, and interpreting efficacy, safety and biomarker data. Works within cross-functional global study teams and mentors less experienced clinical scientists without formal line management.

• Ware
• Lead

Leads analytical strategy for late-phase small molecule products, owning comparability studies, characterisation strategies and specification/stability recommendations across the post-approval lifecycle. Partners in a matrix with R&D, GSC, Technical and Regulatory, defends analytical product strategy in health authority inspections and embeds method knowledge into tech transfers.

PAT

• King of Prussia, United States
• Lead

Leads analytical strategy for late-phase small molecule products, owning comparability studies, characterisation strategies and post-approval change submissions. Partners across R&D, manufacturing sites and regulatory in a matrix, embedding method knowledge into tech transfers and defending strategies during health authority inspections.

PAT

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

Leads cross-functional project teams within Oncology Translational Medicine, coordinating diagnostics, biomarker and clinical development activities with internal groups and external labs and manufacturers. Manages integrated timelines, budgets, contracts and invoices, tracks milestones and risks, and supports regulatory documentation and technical evaluations of diagnostic technologies.

Microsoft Project · Microsoft Word · Microsoft Excel +7

• Singapore - Jurong
• Senior · manages people

Provides end-to-end technical accountability for a product across bulk API manufacturing, formulation and packing, acting as MSAT's single-point decision maker within CMC and supply chain teams. Defines the Product Control Strategy, lifecycle verification and technology strategy, and leads technical lifecycle teams through transfers, regulatory reviews and investigations.

MHRA · FDA · Q7 +3

• Bengaluru Luxor North Tower
• Director · manages people

Oversees internal and external medical writing resources for a therapeutic area, ensuring timely, regulatory-compliant clinical and regulatory content for submissions. Leads resource planning, risk management and continuous improvement, embedding digital tools, content automation and AI into authoring practices while developing high-performing teams.

AI · Dashboards

• Mississauga Milverton Drive
• Director · manages people

Oversees internal and external medical writing resources for a therapeutic area, ensuring timely delivery of regulatory-compliant clinical and safety documentation for submissions. Leads resource planning, risk management and continuous improvement, embedding digital content tools and AI into authoring practices while developing a high-performing team.

AI · Dashboards

• USA - Pennsylvania - Upper Providence
• Senior

End-to-end technical accountability for a product across bulk API manufacturing, formulation and packing, acting as MSAT's single-point decision maker for the Product Control Strategy. Leads Product Technical Lifecycle Teams, technology transfer and regulatory submission reviews, driving continuous verification and improvement plans across the supply chain.

MHRA · FDA · GxP +4

• USA - Pennsylvania - Upper Providence
• Hybrid
• US$189,750 – US$316,250 pa
• Director

Leads precision diagnostics strategy for oncology programmes, defining diagnostic requirements for trials, biomarker selection, assay validation and sample handling. Oversees project plans, budgets and regulatory submissions while managing external diagnostic partners, labs and vendors in a matrixed cross-functional environment.

FDA · EU IVDR · PMDA/MHLW Japan +2