Biotechnology Jobs

• Oxford
• On-site
• Mid-level
• Temporary

Hands-on individual contributor role operating production equipment for mRNA vaccine manufacturing at the Harwell site, following cGMP, SOPs and safety requirements. Involves troubleshooting equipment and digital issues, basic maintenance, documentation with Quality Assurance, and RCA/CAPA investigations, with exposure to continuous improvement and Generative AI tools.

Generative AI

• Oxford
• On-site
• Entry level
• Temporary

Operate manufacturing equipment for mRNA vaccine production under cGMP and SOPs, maintaining documentation, gowning and housekeeping standards. Partner with Quality Assurance on batch disposition, lead root cause analysis and CAPA for deviations, and troubleshoot equipment and digital system issues. Work 100% onsite with digital and Generative AI-enabled manufacturing technologies.

Generative AI

• Stevenage
• On-site
• Entry level

Support GMP compliance in a multi-product cell and gene therapy facility, reviewing batch manufacturing and QC records, managing controlled documentation, and preparing patient-specific labels. Work with cross-functional teams on batch release, quality events and inspection readiness, on a Sunday–Wednesday shift pattern.

• London
• On-site
• Junior

Hands-on lab role in a biology team, running experiments across process development, product testing and platform R&D, maintaining iPSC lines and differentiation cultures, and sharing lab operations duties. Data generated feeds directly into how processes and platforms evolve, with structured training from SOP-based work towards independent execution.

Excel · GraphPad Prism

• Cambridge, United States
• Hybrid · 3 days in office
• Director

Lead end-to-end clinical trial material planning, vendor management, packaging, labeling, inventory and global distribution for an AI-first drug discovery company. Act as the clinical supply authority within a lean Pharmaceutical Sciences & CMC team, building scalable systems and vendor networks while partnering closely with Clinical Operations and CROs.

IRT · RTSM

• Stevenage
• On-site
• Entry level
• Shift work

Hands-on manufacturing role producing autologous cell therapies, with roughly 85% of time spent in a GMP cleanroom operating cell-processing equipment, completing documentation and supporting environmental monitoring. Two levels are open: an entry-level Associate Operator and an Operator I for those with GMP or cleanroom experience who take on cell culture, sampling and drug product inspection duties.

GMP Cleanroom · Cell-Processing Equipment

• 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.

• Cambridge
• Director

Leads business process mapping, design and optimisation across CMC Regulatory Affairs, from development and registration through post-approval lifecycle management. Partners with IT, data owners and cross-functional teams to translate regulatory needs into digital, automation and AI use cases, then drives implementation, adoption and KPI measurement. Distinct for combining regulatory operations expertise with AI-enabled capability building in a global matrixed pharma environment.

Veeva Vault · Planisware · Signavio +2

• Swindon
• On-site
• Entry level
• Permanent

Supports the routine running of a QC Microbiology laboratory: booking in samples, maintaining reagent, media and consumable stock, ordering supplies, performing equipment checks and second-analyst checks, and helping clean classified cleanrooms. Also writes and updates SOPs, specifications and scientific reports while working to GMP standards. No previous laboratory experience is required.

Microsoft Word · Microsoft Excel

• Swindon
• On-site
• Shift work

Operate aseptic filling lines and manufacture pharmaceuticals to SOPs and Batch Manufacturing Records, performing filling, packaging, in-process checks, line changeovers and cleaning. Work in cleanrooms on Double Days, 24/7 or Night shifts, using HMI-controlled CIP/SIP systems, autoclaves and SAP, and support validation and new product introduction.

SAP · HMI · CIP +2

• Glasgow
• £39,906 – £46,049 pa
• Entry level
• Contract

Develops high-throughput Python workflows to analyse coarse-grained molecular-dynamics simulations of engineered protein assemblies, extracting geometric, topological and structural descriptors such as curvature, lumen dimensions and packing order. Builds structure-property relationships and reusable, version-controlled pipelines feeding predictive and active-learning models, within an interdisciplinary team spanning computational chemistry, machine learning, protein science and engineering.

Martini · GROMACS · VMD +2

• IM92AP
• On-site
• £29,000 – £32,000 pa
• Mid-level
• Permanent

The QC Analyst role involves performing quality control testing of raw materials, intermediates, and finished products in a regulated manufacturing environment. Responsibilities include analytical testing, environmental monitoring, and maintaining compliance with GMP standards. The role offers exposure to a variety of analytical techniques and technologies, supporting continuous improvement initiatives.

• London
• Hybrid · 2–3 days in office
• €81,000 – €135,000 pa
• Mid-level
• Contract

Owns defined planning process areas within GSK's ERP Evolution Programme, ensuring the global S/4 Planning template integrates with OMP, APO and other planning tools across Rx and Vx supply chains. Leads design, configuration input, documentation, testing, data migration and business readiness for UAT, cutover and post-go-live support, working with SAP functional experts, GPO, PLM, Quality and site teams.

SAP ECC · S/4HANA · OMP +2

• Leeds
• On-site
• Senior

Lead early-phase clinical trials as Principal Investigator or Project Physician, taking studies from start-up through closeout and the Clinical Study Report. Work across first-in-human studies, multiple therapeutic areas and an NHS Trust collaboration, with on-call cover and mentoring of less experienced physicians.

MHRA · cGMP · NHS Trust

• Harrow
• Remote
• Mid-level

Manage worldwide post-approval regulatory activities for biological and plasma products, focusing on CMC variations, renewals, market expansions and annual reports. Assess change controls, review quality control and production study reports, and coordinate submission content with manufacturing, supply chain and QA teams. Client-dedicated role working in Regulatory Information Management systems such as Veeva Vault.

Veeva Vault · Word · PowerPoint +1