Biotechnology Jobs

• London
• Hybrid
• Director

Provides medical and scientific leadership for pharmacovigilance and risk management of oncology assets in clinical development, interpreting safety data, detecting and escalating signals, and delivering benefit-risk recommendations. Represents Safety on cross-functional clinical matrix teams and governance committees, and interacts with regulatory authorities. Hybrid role based in the UK, Belgium, Poland or Italy.

• Poznan Grunwaldzka
• Hybrid
• £410,250 – £683,750 pa
• Director

Provides medical and scientific leadership in safety evaluation and risk management for oncology assets in clinical development, interpreting safety data, escalating signals and delivering evidence-based benefit-risk recommendations. Leads Safety Review Teams and cross-functional matrix groups, representing Safety to governance committees and regulatory authorities. Hybrid role based in the UK, Belgium, Poland or Italy.

• Livingston
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for a dedicated clinical trial program, ensuring GCP compliance, patient safety and data integrity. Builds relationships with investigators, resolves data queries, mentors junior staff and travels up to 40-60% within the region.

Investigator Site Files · Trial Master Files

• Oxford
• On-site
• Mid-level

Hands-on automation engineering role supporting drug product packaging and drug substance manufacturing at a new mRNA facility. Involves commissioning and optimising Emerson DeltaV and Allen-Bradley/Rockwell PLC systems, automated labelling and secondary packaging equipment, plus GxP validation, root cause analysis and lifecycle documentation. Works independently as a technical specialist across manufacturing, engineering, quality and digital teams.

Emerson DeltaV · Allen-Bradley · Rockwell Automation +7

• Uxbridge
• Director

Serves as primary medical accountability for Phase 1–3 clinical trials in neuroscience, leading medical monitoring, safety assessment and benefit/risk analysis within a matrixed study delivery team. Partners with clinical scientists on protocol design, site interactions and health authority submissions, and builds relationships with principal investigators and thought leaders.

• London
• On-site
• Lead · manages people

Own the manufacture of electromechanical automation systems and sterile GMP plastic consumables, driving yield, quality and cost improvements while scaling volume. Lead greenfield facility build-out, supplier and contract manufacturer management, and grow the manufacturing team alongside the Head of Engineering.

ISO 13485 · ERP · MRP +3

• 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

• Portsmouth
• On-site
• Entry level
• Permanent

Performs laboratory test work in line with SOPs, recording raw data and flagging delays or deviations to management. Reviews testing requirements and safety data, troubleshoots instrumentation, and helps maintain lab systems such as purchasing, calibration and materials inventory. Based on-site in Portsmouth within a validation and lab operations team.

• Slough
• On-site
• Senior
• Permanent

Performs routine, non-routine and stability testing of biologic drug substances using ELISA, cell-based potency assays and Biacore (SPR), while coordinating assay activities and managing project priorities and timelines. Acts as a technical subject matter expert, mentoring colleagues and supporting method development, validation, troubleshooting and GMP-compliant documentation within a client-facing analytical service department.

ELISA · Biacore · Vi-CELL +2

• London
• Hybrid
• Senior

Designs end-to-end data solutions spanning data integration, data warehousing, master data management, governance and analytics for a biopharmaceutical company. Translates business requirements into data models, data flows and integration patterns, and leads architecture and design reviews across enterprise applications and cloud data platforms.

SaaS · APIs · Cloud Data Platforms

• London
• Lead

Serves as subject matter expert in COA endpoint strategy, instrument development and regulatory strategy, advising pharma and biotech sponsors and representing the company as an external scientific thought leader. Leads qualitative research supporting content validity, oversees internal project teams, mentors consultants and supports business development through proposals and client presentations.