Biotechnology Jobs

• Reading
• Mid-level

Shapes and drives end-to-end clinical trial supply strategy, translating study protocols into kit designs, demand forecasts and packaging plans. Oversees vendors, IRT systems, distribution and temperature-excursion management while leading client and vendor meetings. Combines analytical planning with operational leadership across GxP-regulated clinical supply work.

Interactive Response Technology · Microsoft Word · Microsoft Excel +1

• Reading
• Mid-level

Embedded with a global pharmaceutical sponsor, you act as the clinical supply representative in cross-functional study teams, owning supply strategy, vendor oversight and risk mitigation. Work spans protocol interpretation, label text, demand forecasting, packaging campaigns, IRT setup and temperature excursion management, with a strategic rather than operational focus.

IRT · RTSM · ERP +4

• London
• Hybrid
• Mid-level

Drives clinical supply forecasting and IMP budgeting for global trials, translating study protocols and recruitment projections into forecasting tools and monitoring deviations over 3-12 month horizons. Coordinates cross-functional IMP estimation and risk assessment meetings, aligning manufacturing, packaging and distribution to prevent stock-outs, while leading continuous improvement in a matrixed environment.

RTSM · Excel

• Groton, United States
• Hybrid · 2–3 days in office
• US$124,400 – US$207,400 pa
• Lead

Leads the strategy, design and lifecycle management of digital clinical supply chain systems for Global Clinical Supply, working with product managers and business SMEs on a 3-5 year roadmap. Drives process and technology integration, system modernisation and retirement, and enterprise-level portfolio prioritisation while reporting progress to senior management. Hybrid role with up to 15% travel.

• Andover, United States
• Hybrid · 2–3 days in office
• US$124,400 – US$207,400 pa
• Lead · manages people

Lead the digital transformation of Pfizer's clinical supply chain systems, overseeing the full lifecycle from concept to decommissioning. Define multi-year product strategies, drive process and technology integration, and guide cross-functional teams to ensure regulatory compliance and efficient delivery of investigational products worldwide.

• United Kingdom
• Hybrid
• Mid-level

Manages end-to-end clinical trial supply chains, developing study-specific plans, coordinating cross-functional teams, and ensuring GxP-compliant distribution and inventory levels. Represents the department externally, mentors junior staff, and drives process improvements within a global clinical supplies team.

Microsoft Office

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

Sits within GSK's Chemical Manufacturing & Control function, shaping how AI transforms manufacturing sites worldwide. Runs day-to-day tech transfer engagement with sites and CMOs, sizes AI opportunities, defines target process, data and agent architecture, and drives agentification and recipe building for new products alongside forward deployed engineering pods.

MES · LIMS · ERP +6

• Stevenage
• Hybrid · 2–3 days in office
• Senior

Sits within GSK's Chemical Manufacturing & Control function, running day-to-day tech transfer engagement with manufacturing sites and CMOs while redesigning processes in detail. Shapes NPI launch strategy covering site impact assessment, capacity management, digital twins, scenario planning and virtual line commissioning, and defines the target process, data and agent architecture. Owns the tech transfer package and drives agentification and MES-ready recipe building alongside forward deployed engineering pods.

MES · LIMS · ERP +6

• Salt Lake City, United States
• Mid-level
• Contract

Develop, optimize and validate cell-based and biochemical assays for automated high-throughput screening, running workflows at scale across 384- and 1536-well formats. Work in a cross-disciplinary team with biologists, automation and data scientists, documenting methods so assays transfer reliably. A 9-month contractor role, Monday to Friday, 9am-5pm.

Liquid Handlers · Plate Readers · Imagers +5

• Cambridge, United States
• Hybrid · 3 days in office
• Director

Lead end-to-end clinical trial material planning, vendor management, packaging, labeling, inventory and global distribution for an AI-first drug discovery company. Act as the clinical supply authority within a lean Pharmaceutical Sciences & CMC team, building scalable systems and vendor networks while partnering closely with Clinical Operations and CROs.

IRT · RTSM

• United Kingdom
• Remote
• Lead

Supports central comparator sourcing for clinical trials on a client-dedicated FSP team, covering market intelligence, sourcing recommendations, and purchase order execution across EMEA. Acts as an SME on the external comparator landscape, advising on regional and central/local sourcing strategy while escalating quality or temperature issues to the client.

• Harrow
• Remote
• Mid-level

Manage worldwide post-approval regulatory activities for biological and plasma products, focusing on CMC variations, renewals, market expansions and annual reports. Assess change controls, review quality control and production study reports, and coordinate submission content with manufacturing, supply chain and QA teams. Client-dedicated role working in Regulatory Information Management systems such as Veeva Vault.

Veeva Vault · Word · PowerPoint +1

• Cambridge
• Hybrid · 3 days in office
• Director

Leads an integrated Business Continuity and Crisis Management capability across Oncology R&D, owning the framework, risk registers and BIAs while designing executive-level crisis exercises. Drives emerging-risk assessment, supply-chain nth-tier visibility and the practical use of AI in resilience practice, acting as the audit and regulatory interface for standards such as NIS2.

NIS2 · Business Continuity Software

• London
• Hybrid
• Lead · manages people

Serves as the clinical trial pharmacy subject matter expert across global oncology programmes, advising on investigational product handling, preparation, storage and accountability, and on hazardous drug and CSTD requirements. Develops pharmacy manuals and training for site pharmacists and study teams, supports audits and CAPAs, and oversees FSP pharmacists and external vendors. Hybrid role spanning London, Paris or Cambridge MA.

Closed System Transfer Devices

• Cambridge
• Senior
• Temporary

Hands-on upstream process development role delivering mammalian cell culture studies, including CHO-based fed-batch and perfusion processes, media and feed optimization, and bioreactor operation from ambr systems to bench-scale stirred tanks. Works under minimal supervision within a matrix CMC team, applying DoE and statistical analysis, supporting scale-up and tech transfer to GMP and CMO partners, and providing day-to-day technical coordination to technicians and operators.

ambr · ambr250 · Stirred-Tank Bioreactors +6