Biotechnology Jobs

• Kingsfold
• On-site
• £16 ph
• Entry level
• Temporary

Picking and packing client orders, receiving courier deliveries into inventory software, and following production orders for packaging in a GMP-regulated pharmaceutical environment. Involves cycle counts, waste disposal, SOP compliance and continuous improvement, working in ambient, refrigerated and frozen conditions down to -20°C.

Inventory Software

• Oxford
• On-site
• Entry level
• Permanent

Hands-on laboratory role supporting microbiology, molecular biology, sample processing and sequencing within the Pathogen Applications Team. Involves receiving and tracking clinical samples, preparing microbial cultures, running qPCR and sequencing workflows, and maintaining QC and documentation. Suits an early-career scientist with practical lab experience in a diagnostic or high-throughput environment.

Sequencing · Oracle Cloud

• Reading
• Mid-level

Embedded with a global pharmaceutical sponsor, you act as the clinical supply representative in cross-functional study teams, owning supply strategy, vendor oversight and risk mitigation. Work spans protocol interpretation, label text, demand forecasting, packaging campaigns, IRT setup and temperature excursion management, with a strategic rather than operational focus.

IRT · RTSM · ERP +4

• Reading
• Senior

Embedded with a global pharmaceutical sponsor, you own end-to-end clinical supply strategy across complex trials: protocol interpretation, label text, demand forecasting, packaging, IRT setup, distribution and temperature-excursion management. You lead vendor oversight, risk assessments and budget tracking while advising study teams and client leadership.

IRT · RTSM · ERP +3

• United Kingdom
• Remote
• Senior

Monitors investigator sites using a risk-based approach, conducting remote and on-site visits to assess protocol and regulatory compliance, performing SDR, SDV and CRF review, and documenting findings in reports. Acts as a site processes specialist ensuring trials follow ICH-GCP, applicable regulations and SOPs, while developing collaborative relationships with investigational sites and supporting audit readiness.

CTMS · Microsoft Office

• London
• On-site
• Mid-level

Owns end-to-end purchasing, invoicing and inventory for both electromechanical automation systems and GMP-grade sterile fluidic consumables, spanning supplier qualification, cost-down programmes and demand planning. Reports to the Hardware Lead and works across manufacturing, biology, engineering, quality and finance, building ERP/MRP-based planning in a hands-on, on-site role.

ERP · MRP

• Oxford
• On-site
• Lead
• Permanent

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.

ELN · LIMS

• Oxford
• Hybrid
• Entry level
• Internship

A 12-month industrial placement within a biotechnology company's community affairs team, based at an Oxford learning lab dedicated to STEAM education. The role involves developing and delivering hands-on science lessons with local schools, preparing lab materials and reagents, managing supplies, and supporting volunteers and scientists. It combines science communication and outreach with practical lab and administrative duties.

• Herzliya, Israel
• Lead

Drive external deal flow by building relationships across innovation hubs, universities, venture capital and corporate venture groups, then match opportunities to internal capability gaps. Own end-to-end partnership management, from screening and diligence through negotiation, vendor onboarding and contracting, while providing outside-in analysis on investment memos and assessing technical novelty.

• US - East Coast
• Director · manages people

Leads identification, evaluation and execution of strategic partnerships, licensing, M&A and co-development deals, from sourcing through due diligence, structuring and closing. Represents the company to biotech, pharma and academic partners, monitors competitive and market dynamics, and advises executive leadership on external innovation strategy post-launch.

• London
• Freelance

Monitors Phase I-IV clinical trials across UK sites, conducting evaluation, initiation, interim and close-out visits in line with GCP and sponsor requirements. Works closely with the Clinical Trial Manager and Lead CRA, handling source verification, eCRF/EDC data review, query resolution and site training. Requires oncology monitoring experience and involves travel plus mentoring of less experienced CRAs.

EDC · eCRF

• 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