Biotechnology Jobs

• London
• Hybrid
• Director

Leads the design and delivery of health economics and outcomes research (HEOR) evidence for a portfolio of HIV treatment and prevention medicines, spanning real-world evidence, clinical outcome assessments, evidence synthesis and economic modelling. Sets COA and patient-centred outcomes strategy, partners with R&D, medical affairs, market access and external payers/HTA bodies, and oversees study quality, compliance and budget within a matrix organisation.

• London
• Hybrid · 2–3 days in office
• Mid-level

Lead advanced analytics projects within ViiV's Medical function, translating strategic priorities into analytical approaches, measurement frameworks and actionable insights. Build models, oversee dashboard design with vendors, and advance AI/ML and agentic workflows across Medical Analytics while partnering with Commercial, Digital and Data Governance teams.

Python · R · SQL +1

• Guildford
• Mid-level
• Permanent

Hands-on laboratory role analysing pharmaceutical samples including APIs, medicines, herbal products and packaging for MHRA Laboratories. Uses HPLC, GC, GC/LC-MS, IR, Raman, UV, dissolution and wet chemistry, with responsibility for drafting reports, validating data, equipment calibration and maintaining an ISO/IEC 17025 quality system. Works within a team of around 30 analytical scientists, independently coordinating project workloads.

Microsoft Word · Microsoft Excel

• United Kingdom
• Remote
• Mid-level

Coordinates and oversees clinical trial activities for assigned studies, including regulatory document review, (e)TMF management, and site file compilation. Provides finance support such as raising POs, vendor creation, budget tracking and invoicing using CERPS, Ariba, Fiori and Veeva Payments. Trains new staff and works within a matrixed FSP team.

Veeva Payments · CERPS · Ariba +5

• London
• Remote
• Mid-level

Manages a portfolio of clinical research studies end to end, leading cross-functional teams and client relationships for Patient Cloud products such as eCOA/ePRO, eConsent and virtual trials. Involves risk assessment, study documentation and milestone tracking, with flexibility needed to work American time zones.

MS Office Suite · Google Workspace

• Maidenhead
• Mid-level

Oversees vendor delivery of medical evaluations for individual case safety reports, applying medical and scientific judgment on causality, expectedness and seriousness. Trains Medical Evaluators, sets assessment frameworks and drives process improvements across Global Safety and Pharmacovigilance. Requires deep pharmacovigilance knowledge and cross-functional stakeholder work.

• Macclesfield
• On-site
• Senior
• Permanent

Perform routine and non-routine analytical testing of pharmaceutical oral drug products and new modalities using HPLC, Karl Fischer, dissolution and mass spectrometry. Review data for GLS and GMP compliance, investigate out-of-specification results, and develop, optimise and validate analytical methods while training colleagues and driving continuous improvement at a client's Macclesfield facility.

HPLC · Karl Fischer · Mass Spectrometry +1

• Macclesfield
• On-site
• Mid-level
• Permanent

Perform routine and non-routine analytical testing of pharmaceutical oral drug products and new modalities using HPLC, Karl Fischer, dissolution and mass spectrometry. Review data for GLS and GMP compliance, investigate out-of-specification results, and develop and validate analytical methods while training colleagues and supporting client projects at a Macclesfield pharma facility.

HPLC · Karl Fischer · Mass Spectrometry +1

• Huntingdon
• On-site
• Entry level

Performs laboratory-based technical and operational support for in vivo genetic toxicology studies, including the in vivo micronucleus test and COMET assay, under GLP and SOP compliance. Duties cover cell stock maintenance, reagent and media preparation, calibration checks, slide preparation, accurate data recording, QC checks and stock takes, with findings reported to the Study Director.

HASAWA · COSHH

• Reading
• Senior

Conducts site qualification, initiation, monitoring and close-out visits for a dedicated sponsor program, ensuring GCP compliance, patient safety and data integrity. Builds investigator relationships, resolves queries, maintains inspection-ready documentation and mentors junior team members, with up to 40-60% regional travel.

Investigator Site Files · Trial Master Files

• Reading
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for a pharmaceutical sponsor as an embedded member of IQVIA's Clinical Functional Service Partnership team. Monitors patient safety, data integrity and protocol compliance, mentors junior staff, and travels up to 40-60% of the time within the region.

Investigator Site Files (ISF) · Trial Master Files (TMF)

• London
• On-site
• Director
• Permanent

Leads CMC regulatory strategy for global submissions including IND, CTA, BLA and MAA, and oversees agency correspondence and compliance for mRNA products. Reviews submissions for readiness, drives health authority interactions, and advises manufacturing and quality teams on change controls and regulatory guidance across vaccines, oncology and rare disease programmes.

IND · CTA · BLA +1

• London
• On-site
• Entry level
• Internship

A 12-month industrial placement in Pfizer's Peptide Drug Product Development group, working alongside formulation scientists and analytical chemists. The role involves preparing and evaluating peptide formulations, running solubility and stability studies, and gaining hands-on experience with HPLC/UPLC and biophysical characterisation methods.

HPLC · UPLC

• Woking
• On-site
• Senior

Owns the product and go-to-market strategy for Digital CMC at IDBS, identifying high-value opportunities to digitise CMC development, submission readiness, technology transfer and lifecycle management. Translates real-world CMC problems into business cases and roadmap priorities, applying structured scientific data, workflow automation and agentic AI. Market-facing role reporting to the Director, Strategic Operations, partnering with biopharma customers and cross-functional teams.

ELN · LIMS · MES +7

• Bedford
• On-site
• £41,832 pa
• Mid-level · manages people

Hands-on leadership of a pharmaceutical warehouse shift, overseeing receipt, storage and dispatch of chilled and controlled drugs while managing and developing a team. Ensures MHRA compliance through audits, root cause analysis and CAPAs, plus health and safety, budget monitoring and continuous improvement of workflows.

WMS · Six Sigma