Biotechnology Jobs

• Greater Poland
• Hybrid · 2–3 days in office
• €87,000 – €145,000 pa
• Director
• Permanent

Provides medical and scientific expertise in safety evaluation and risk management for GSK assets across clinical development and post-marketing settings. Leads signal detection, benefit-risk assessment, regulatory periodic reports and RMPs, working within a global cross-functional matrix alongside Clinical Operations, Regulatory and Biostatistics. Distinct for its strong focus on pharmacovigilance governance, safety strategy and scientific writing.

ICH · GVP · CIOMS

• London
• Hybrid · 2–3 days in office
• €87,000 – €145,000 pa
• Director
• Permanent

Provides medical and scientific expertise in safety evaluation and risk management for GSK assets across clinical development and post-marketing settings. Leads signal detection, periodic regulatory reports, RMPs and benefit-risk assessments within a global cross-functional matrix, presenting complex safety issues to senior governance committees. Distinct for its blend of pharmacovigilance strategy, regulatory writing and matrix leadership.

ICH · GVP · CIOMS

• 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

• Grimsby
• Entry level
• Permanent

Performs registration, preparation and analysis of samples, reading plates and validating results to required quality standards. Prepares media and QC, maintains records and HSE compliance, and supports continuous improvement and UKAS accreditation. Full-time, 37.5 hours over two shift patterns including weekends.

UKAS · ISO

• Barcelona, Spain
• Hybrid
• €63,600 – €118,000 pa
• Lead · manages people

Lead and develop a team of Central Monitors, shaping central and site monitoring strategies across a global development portfolio. Oversee trial-data surveillance, risk reviews and signal detection using Central Monitoring technology, translating complex risk signals into actionable insights for Clinical Trial Teams. Partners with clinical, data and risk-surveillance teams to strengthen risk-based monitoring and Risk-Based Quality Management.

Artificial Intelligence

• 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

• Harrow
• Remote
• Lead · manages people

Acts as functional lead on the core project team, driving site identification and country selection for clinical trials from award onwards. Designs protocol-specific site questionnaires, leads local teams through surveys, models enrolment scenarios, and presents data-driven strategies to sponsors. Also serves as SME for feasibility systems and may lead stand-alone feasibility studies.

• London
• On-site
• Senior

Finance lead for a designated disease area with full P&L ownership across UK & Ireland in-line and pipeline assets. Drives strategic planning, budgeting, monthly forecasting and pricing/reimbursement business cases, applying AI and advanced analytics, while partnering Commercial, Medical, Market Access and Global Finance. Office-based in London with at least 60% attendance.

AI

• Cambridge
• Hybrid · 3 days in office
• Senior

Lead UK direct tax compliance and group tax reporting for a FTSE 100 biopharmaceutical business, preparing and reviewing corporation tax computations, patent box and capital allowance claims, and quarterly and year-end tax provisions under Sarbanes-Oxley. Handle HMRC audit queries and negotiations, advise the UK business on legislation changes, and drive process efficiencies through automation and AI.

AI

• Reading
• Hybrid
• Mid-level

Supports clinical trials by designing, setting up and maintaining Interactive Response Technology (IRT) solutions, translating supply requirements into system specifications. Contributes to risk assessments, user acceptance testing and validation documentation, and advises study teams on IRT processes. Works with cross-functional global stakeholders on study startup, amendments and continuous improvement.

IRT · RTSM · IVRS +1

• London
• Remote
• Mid-level

Oversees medical coding activities across clinical studies, managing coding dictionaries such as MedDRA and WHODrug, reviewing coded data for accuracy and compliance, and preparing coding reports for medical review. Acts as subject matter expert, delivering training and partnering with Clinical Development, Pharmacovigilance and Data Management teams to drive process improvements and regulatory compliance.

MedDRA · WHODrug

• United Kingdom - Walton Oaks
• Senior

Conduct strategic regulatory activities for assigned products and markets, managing Marketing Authorisation applications, variations, renewals and NRA queries. Work with cross-functional teams and above-country hubs to maintain compliance, support clinical trial applications and share regulatory intelligence.

• 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

• Reading
• Remote
• Senior
• Permanent

Supports Pharmacometrics by programming, validating and delivering NONMEM-ready PK/PD datasets from SDTM/ADaM sources using advanced R, covering pre-lock and post-lock clinical data. Includes QC of datasets from external partners and of custom R packages, plus liaison with Data Management, Biostatistics and Bioanalytical teams and regulatory submission deliverables.

R · NONMEM · SDTM +1