Biotechnology Jobs in Leicester

Associate Director, Safety Epidemiology – Global Patient Safety

Lead the design and execution of post-authorisation safety studies using real-world data to assess and communicate the safety profiles of AstraZeneca’s medicines. Provide strategic epidemiological input to regulatory submissions, safety signal evaluations, and diversity initiatives, collaborating with internal teams and external partners. Drive methodological excellence in pharmacoepidemiology and contribute to global patient safety decision-making across a broad product portfolio.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Associate Director, R&D Project Management

Leads the operational delivery of high-impact, global R&D projects within a cross-functional biotech environment. Focuses on strategic planning, budget and timeline management, risk mitigation, and stakeholder reporting. Provides mentorship to junior project management staff and ensures robust project execution across drug research, development, and manufacturing.

CSL

Hybrid Permanent

Biologics Account Manager

This role involves driving clinical demand for respiratory biologics by building strategic relationships with healthcare professionals and multi-disciplinary teams across a defined UK territory. The Account Manager will lead formulary access, support homecare utilization, and collaborate with cross-functional teams to implement account plans in complex secondary care environments. Success requires strong commercial acumen, stakeholder influence, and deep understanding of the NHS commissioning landscape.

AstraZeneca Sheffield, United Kingdom

On-site Permanent

(Fixed Term) Manufacturing Associate I

Operate and maintain mRNA vaccine production equipment in compliance with cGMP and safety standards, executing manufacturing processes, troubleshooting equipment and digital systems, and supporting quality documentation and continuous improvement initiatives. Work within a cross-functional team to ensure timely batch release and operational excellence in a fast-paced, highly regulated environment.

Moderna Oxford, United Kingdom

On-site Temporary

(Fixed Term) Manufacturing Associate I

Operate production equipment for mRNA vaccine manufacturing in compliance with cGMP and safety standards. Perform routine maintenance, support deviation investigations, and contribute to continuous improvement in a highly regulated, technology-driven environment. Work collaboratively with QA and cross-functional teams to ensure timely batch disposition and operational excellence.

Moderna

On-site Temporary

Associate Director, Clinical Trial Disclosure & Transparency

This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA 801, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while managing redaction of confidential information for public release. They act as a key liaison with regulatory bodies and internal teams, driving process efficiency and vendor performance across the clinical development lifecycle.

CSL

Associate Principal Scientist - In Vivo Pharmacology

Lead and direct in vivo pharmacology studies within multidisciplinary teams to advance preclinical drug discovery programmes targeting kidney diseases such as CKD, AKI, and diabetic nephropathy. Design and interpret translational studies using disease models, support target validation, and guide therapeutic development through biomarker and efficacy analysis. Collaborate with biotech and pharma partners while mentoring scientists and shaping scientific strategy.

Proclinical Nottingham, Nottinghamshire, United Kingdom £50,000 – £500,000 pa

Analytical Chemist, Pharmaceutical (HPLC) 12 month fixed term

Perform analytical and stability testing of pharmaceutical and nutraceutical products using HPLC, GC/MS, and wet chemistry techniques in a GMP-regulated environment. Responsibilities include data entry into LIMS, equipment calibration, troubleshooting, and supporting audit readiness. The role also involves training junior staff and contributing to quality investigations and cross-laboratory support.

NMS Recruit Ltd t/a Russell Taylor Group Swadlincote, Derbyshire, DE11 0AG, United Kingdom £30,000 – £33,956 pa

On-site Contract

Production Process Engineer

Production Process EngineerCastle Donington, DerbyshireAre you passionate about continuous improvement and process efficiency? Do you want to play a key role in helping a growing employee-owned manufacturing business achieve its lean, quality and productivity goals?We are looking for an experienced...

Medstrom Diseworth, Leicestershire, DE74 2QD, United Kingdom £48,000 pa

Service Engineer

We're not just looking for an already-qualified service engineer - we're looking for someone who's spent time troubleshooting lab or clean air equipment and wants to build a career around it.We're recruiting on behalf of a specialist manufacturer of laboratory...

H Squared Talent Ltd Cossall, Nottinghamshire, United Kingdom £33,000 – £37,000 pa

Validation/ Quality Assurance Specialist, Pharmaceutical

The Validation/Quality Assurance Specialist will plan and execute validation activities, author and maintain validation protocols, and collaborate with cross-functional teams to ensure compliance with GMP standards. The role involves maintaining validated status, supporting regulatory inspections, and contributing to the Site Validation Master Plan.

NMS Recruit Ltd t/a Russell Taylor Group Swadlincote, Derbyshire, DE11 0AG, United Kingdom £30,000 – £34,000 pa

On-site Permanent

Mechanical Design Engineer

Cure Talent is delighted to partner a leading UK manufacturer specializing in the design and production of high-quality packaging machinery solutions for the medical device industry.We are seeking a Mechanical Design Engineer to join this company’s engineering team. The ideal...

Cure Talent Castle Donington, Leicestershire, United Kingdom £35,000 – £45,000 pa