Biotechnology Jobs

• Durham, United States
• Hybrid
• US$222,750 – US$371,250 pa
• Director

Leads end-to-end Model-Informed Drug Development and clinical pharmacology strategy across the drug development lifecycle, from first-in-human studies through filing and lifecycle management. Coordinates CPMS activities across assets, approves study designs and regulatory documents, and partners with digital medicine, translational imaging, biostatistics and AI/ML teams. Reports into the Respiratory, Immunology & Inflammation Research Unit within the new Clinical Pharmacology and Quantitative Medicine organisation.

MIDD · QSP · AI/ML

• Stevenage
• Hybrid · 2 days in office
• US$242,250 – US$403,750 pa
• Director · manages people

Leads the global development of a medicine from clinical Proof of Concept to approval in first major markets, acting as single point of accountability. Builds and directs a matrixed Medicine Development Team spanning clinical, medical, commercial and manufacturing, driving strategy, governance and go/no-go decisions. Hybrid role with at least two days on-site per week.

• Oxford
• On-site
• Mid-level · manages people
• Permanent

Leads the end-to-end event delivery workflow for gene edited and transgenic crops, from transformation output through sampling, molecular confirmation, QC review and handover. Designs and validates genotyping assays (PCR, qPCR, ddPCR, KASP, NGS) and builds stage-gate criteria, LIMS-enabled tracking and vendor strategies across corn and wheat programmes.

Endpoint PCR · qPCR · ddPCR +6

• United Kingdom
• Remote
• Senior

Acts as independent Principal Investigator overseeing qualitative in-trial research studies, from design through delivery, for pharmaceutical clients. Applies methods like interviews and surveys to capture patient experience data, manages project budgets and timelines, and contributes to proposals and client development. Requires CAQDAS expertise and strong scientific writing.

Atlas.ti · NVivo · MAXQDA +1

• Macclesfield
• On-site
• Senior
• Permanent

Designs and executes work plans for early drug discovery projects within a Protein Sciences team, supporting multiple projects and presenting results to clients. Hands-on role focused on recombinant protein expression using insect cell systems such as BEVS, S2 and Sf9, including construct design, baculovirus generation and troubleshooting difficult targets like membrane proteins.

BEVS · Sf9 · Sf21 +2

• Oxford
• On-site
• £40,000 pa
• Senior
• Permanent

Develops and optimises LC-MS workflows for low-input and single-cell proteomics and/or metabolomics, supporting researchers across the institute with experiment design, method development, data acquisition and interpretation. Works closely with bioinformatics, scientific computing and AI/ML teams, and helps build SOPs and training material for single-cell MS capability.

LC-MS · Flow Cytometry · Sequencing +5

• Burgess Hill
• Hybrid
• £49 – £86 ph
• Lead
• Contract

Leads authoring, review and lifecycle management of clinical and performance evaluation documentation for a global diagnostics organisation, including protocols, study reports, investigator brochures and regulatory submissions. Works cross-functionally with regulatory, quality, R&D and medical affairs teams, conducting literature reviews and synthesising complex clinical data under IVDR and GCP.

AI-enabled tools

• Cambridge
• On-site
• Entry level
• Contract

Hands-on laboratory role supporting a state-of-the-art multiomics facility, running Illumina and Nanopore sequencing, bulk RNA/DNA library prep and single-cell workflows such as 10x Genomics and Parse Bio. The post also covers lab automation, instrument maintenance, SOPs, purchasing and advising researchers on experimental design within a collaborative core-facility team.

Illumina · Nanopore · 10x Genomics +3

• London
• Lead

Ensures clinical trials comply with quality standards, SOPs and health authority regulations, partnering with site management and therapeutic area leads. Builds cluster quality plans, leads CAPA and root cause investigations, and supports audit and inspection readiness across internal and FSP teams. Also handles local regulatory intelligence and supplier quality assessments.

Quality Risk Management System

• London
• Hybrid
• Director · manages people

Leads the development and execution of international regulatory strategy across European and Rest of World markets, from first-in-human through post-marketing. Represents Global Regulatory Affairs on core development teams, manages project plans and resources, and advises senior management. Also a people manager within the International GRA leadership team, driving process improvement and regulatory policy engagement.

EMA

• 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

• 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

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

Hands-on health economics role leading the delivery of cost-utility and budget impact models in Excel and VBA for national HTA submissions to NICE, SMC and AWMSG. Partners with UK Market Access, Medical and Brand teams plus the global HEOR function, and also builds early cost-effectiveness models for future brands and indications.

Microsoft Excel · Microsoft VBA

• Belfast
• £35,000 – £37,532 pa
• Entry level
• Contract

A graduate-level KTP Associate role based at Norbrook Laboratories, working within the R&D team to develop a data-driven framework for pharmaceutical scale-up of liquid dosage veterinary medicines. The project focuses on predictive modelling of process parameters and product quality across scales, combining chemical engineering principles with statistical and hybrid data modelling, delivered in collaboration with Queen's University Belfast's School of Pharmacy.

• 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