Biotechnology Jobs

• London
• Hybrid
• PLN 228,000 – PLN 380,000 pa

Designs disease data information models for priority discovery areas, writing mapping rules to harmonise biomedical data and building quality checks that keep models trustworthy. Works hands-on in code and modelling tools, using AI assistants daily, and partners with research, ontology and data platform teams to get models adopted.

NCI Thesaurus · MONDO · EFO +6

• Warsaw, Poland
• Hybrid
• PLN 228,000 – PLN 380,000 pa

Designs disease data information models for priority discovery areas, writing mapping rules to harmonise biomedical data and building quality checks to keep it trustworthy. Works hands-on in code and modelling tools, using AI assistants daily, and partners with research, ontology and data platform teams plus external partners.

NCI Thesaurus · MONDO · EFO +6

• London
• Hybrid · 2 days in office
• Director

Provides medical and scientific leadership for pharmacovigilance and risk management of HIV assets in clinical development, interpreting safety data, detecting signals and delivering benefit-risk recommendations. Represents Safety on cross-functional matrix teams and governance committees, and interacts with regulators and external experts. Hybrid role based in London with at least two days per week on site.

• London
• Hybrid · 2 days in office
• Director

Provides medical and scientific leadership in pharmacovigilance and risk management for key HIV assets, leading safety strategy, signal detection and benefit-risk evaluation across clinical development and post-marketing. Represents the company on cross-functional matrix teams and with regulatory authorities, and leads inspection readiness and process improvement.

• Durham, United States
• Senior

Acts as the technical single point of accountability for a product across its lifecycle, from bulk API manufacturing and formulation through packing and support activities. Leads Product Technical Lifecycle Teams, defines the Product Control Strategy and end-to-end performance qualification, and coordinates Drug Substance, Drug Product, Analytical and Device leads within MSAT.

ICH Q7 · ICH Q8 · ICH Q9 +2

• London
• Director · manages people

Oversees internal and external medical writing resources within a therapeutic area, ensuring timely delivery of regulatory-compliant clinical and regulatory content for medicines and vaccines. Leads resource planning, risk management and continuous improvement, embedding digital tools and AI to accelerate submissions while developing high-performing teams.

AI · Dashboards

• Barnard Castle
• Director

Supports the Value Stream Operations Manager in running a sterile manufacturing value stream, coordinating daily and weekly performance across Operations, Engineering, Quality, Supply Chain and MSAT. Drives safety, quality, delivery and cost objectives, leads continuous improvement using Lean and Six Sigma, and deputises for the Operations Manager when required.

GSK Production System

• Ware

Acts as the technical-functional expert for Siemens Opcenter Execution Pharma within a global supply chain digital function, guiding MES engineers, architects and delivery partners on standard and custom functionality. Owns functional design of Process Instructions and workflows, troubleshooting, testing and validation, while ensuring GxP, GAMP and data integrity compliance.

Siemens Opcenter Execution Pharma · Siemens Opcenter · ERP

• Worthing
• Senior

The Molecule Steward holds end-to-end technical accountability for a product across its lifecycle, from bulk API manufacturing and formulation to packing and support activities. They represent MSAT in defining the Product Control Strategy, coordinate Drug Substance, Drug Product and Analytical leads, and lead Product Technical Lifecycle Teams to resolve technical issues and drive improvement plans.

MHRA · FDA · ICH Q7 +3

• Barnard Castle
• 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 · ICH Q7 +3

• Ware
• Senior

End-to-end technical accountability for a small molecule product across its lifecycle, from bulk API manufacturing and formulation to packing and regulatory submissions. Represents MSAT as technical single-point decision maker, leads Product Technical Lifecycle Teams, and defines control strategy, technology transfer and continuous verification across supply nodes.

MHRA · FDA · ICH +4

• Waltham, 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, clinical development, regulatory and finance activities across internal groups and external partners. 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

• London
• Hybrid
• US$189,750 – US$316,250 pa
• Director

Leads precision diagnostics strategy for oncology programmes, defining diagnostic requirements for trials and overseeing biomarker selection, assay validation and sample handling. Manages project plans, budgets and timelines while engaging diagnostic companies, clinical labs and vendors, and supporting regulatory submissions. Works cross-functionally with research, clinical, regulatory and commercial teams in a hybrid model.

FDA · EU IVDR · PMDA +2

• Stevenage
• Hybrid
• Director

Leads precision diagnostics strategy for oncology programmes, defining biomarker selection, assay validation and sample collection across multiple assets. Oversees project plans, budgets and regulatory submissions while managing external diagnostic partners and clinical labs. Hybrid role based in Stevenage, relocating to Cambridge by early 2029.

FDA · EU IVDR · PMDA/MHLW Japan +2

• Waltham, United States
• Hybrid
• US$189,750 – US$316,250 pa
• Director

Leads precision diagnostics strategy for oncology programs, defining diagnostic requirements for trials and overseeing biomarker selection, assay validation, and sample collection. Partners cross-functionally with research, clinical, regulatory, and commercial teams, and engages external diagnostic companies and labs to accelerate assay development. Hybrid role based in Waltham, MA.

FDA · EU IVDR · PMDA/MHLW Japan +2