Biotechnology Jobs

Ellison Institute of Technology · Oxford

Leads vector design strategy for gene edited and transgenic crop programmes, covering expression cassette architecture, guide RNA modules, donor templates and multiplex editing configurations. Owns the design-to-vector-release process, including construct QC, sequence management, vendor workflows and handover packages for transformation teams. Builds an industrial-grade vector design capability for corn, wheat and other strategic species, with SOPs, LIMS/ELN tracking and mentoring of scientists.

Ellison Institute of Technology · Oxford

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.

GSK · Zug, Switzerland · US$242,550 – US$404,250 pa

Senior physician leader providing medical oversight, safety evaluation and clinical data interpretation across lung cancer studies within a clinical programme team. Partners with the Senior Scientist and cross-functional groups on protocol design, regulatory interactions and external scientific engagement, while mentoring Medical Directors. Requires an on-site presence of at least two days a week at a GSK site.

GSK · Waltham, United States · US$222,750 – US$371,250 pa

Serves as the physician on oncology clinical programme teams for lung and head/neck cancers, leading medical monitoring, safety oversight and clinical data interpretation across Phase I–III studies. Partners with a Senior Scientist and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement, with on-site presence 2–3 days per week.

TRS Consulting · Birmingham · £50,000 – £55,000 pa

Servicing, installing, calibrating and repairing sophisticated laboratory automation and medical device systems at customer sites across Europe, including pathology departments, university research labs and pharmaceutical facilities. The role is heavily customer-facing and requires around three nights away from home per week, working on high-value electronics and electro-mechanical capital equipment.

TRS Consulting · Leeds · £50,000 – £55,000 pa

Servicing, installing, calibrating and repairing sophisticated laboratory automation and medical device systems at customer sites such as pathology departments, university research labs and pharmaceutical facilities. The role is heavily field-based, involving extensive European travel with around three nights away from home each week, and suits an electro-mechanical or electronics engineer with a customer-facing service background.

AstraZeneca · Norwich

Field-based medical role providing scientific leadership across the NHS haemato-oncology landscape in the North West, Midlands and East of England. You build insight-led territory plans, engage stakeholders through digital and in-person channels, support research and evidence generation, and translate field insights into cross-functional action while complying with the ABPI Code.

AstraZeneca · Cambridge

Field-based medical role providing scientific leadership across the NHS haemato-oncology landscape in the North West, Midlands and East of England. You will lead territory ecosystem planning, build trusted stakeholder partnerships, support research and evidence generation, and use digital channels to translate field insights into action while complying with the ABPI Code.

Ipsen · London

Field-based medical affairs role acting as a scientific partner to healthcare professionals and thought leaders across the East Midlands, Yorkshire and East of England. Involves non-promotional scientific exchange, medical education, advisory boards, and supporting investigator-sponsored and real-world evidence studies within a neuroscience portfolio, working closely with UK, Ireland and global teams.

IQVIA · Livingston

Coordinates laboratory study setup for a clinical research organisation, covering protocol and budget review, database setup, project plans, timelines and documentation. Presents protocol materials at kick-off and investigator meetings, manages scope changes and budget monitoring, and works with project management to improve processes across global Phase I-IV trials.

EMBL-EBI · Saffron Walden · £3,452 pm

Maintains microbial genomes in Ensembl, loading new annotations, coordinating releases and diagnosing data issues. Develops functional annotation and pangenome pipelines, evaluates taxon-specific annotation tools, and builds Nextflow or Snakemake workflows with Python, relational databases and HPC or cloud infrastructure.

Parexel · London

Leads cross-functional clinical trial teams for large pharma partnership clients, owning project plans, budgets, P&L, risk management and client relationships from Phase I to III. Requires strong CRO experience and oncology therapeutic expertise, with fully remote home-based working in a specified EMEA country.

Moderna · Oxford

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.

Moderna · Oxford

Hands-on maintenance of GMP manufacturing equipment at a new mRNA vaccine facility, including autoclaves, filling lines, isolators, TFF systems and chromatography skids. Acts as first responder to equipment failures, performing structured root-cause troubleshooting, preventative maintenance, CAPA work and cGMP documentation, while coordinating vendors and contractors. Includes on-call rotation for 24/7 operations and OJT delivery.

IQVIA · Reading

Monitors oncology clinical trial sites through selection, initiation, monitoring and close-out visits, ensuring GCP and ICH compliance. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within a biotech-focused team supporting emerging biopharma sponsors.