What types of biotech roles are common in Cambridge?

Common roles include research scientists, bioinformaticians, clinical trial managers, and bioprocess engineers.

Are there opportunities for remote work in Cambridge's biotech sector?

While many roles require on-site presence, there are increasing opportunities for hybrid and remote work, especially for data-focused positions.

What are the key industries in Cambridge's biotech sector?

Key industries include genomics, pharmaceutical R&D, bioprocessing, and gene therapy.

How does the academic environment in Cambridge influence the biotech industry?

The strong academic presence, particularly from the University of Cambridge, fosters a culture of innovation and collaboration, driving advancements in biotechnology.

Biotechnology Jobs in Cambridge

Home to world-class research institutions and a thriving biotech ecosystem, Cambridge is a hub for innovation in genomics, pharmaceuticals, and bioprocessing.

Open roles

Salary range

£40k – £100k

Hiring companies

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Cambridge is renowned for its cutting-edge biotechnology sector, driven by a concentration of leading research institutions, universities, and innovative companies. The city hosts a vibrant ecosystem where academic excellence meets commercial ambition, making it a prime location for biotech professionals. Key players such as the Wellcome Sanger Institute and AstraZeneca are headquartered here, alongside numerous scaleups and research-heavy startups. The local biotech landscape is characterised by a strong focus on genomics, pharmaceutical R&D, and bioprocessing, with a mix of on-site and hybrid working arrangements.

Salary on the board

£40k – £100k

Based on advertised midpoints across the 13 priced listings posted in the last 12 months. Base salary only.

By seniority

£k base

Entry

1 job

Junior

1 job

Mid

6 jobs

Senior

100

2 jobs

Lead

3 jobs

Live jobs

81 live roles

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Executive Director, Regulatory Affairs Strategy - Cell Therapy

This role leads global regulatory strategy for high-profile cell therapy programs, shaping end-to-end development from discovery to approval. The individual will direct complex health authority engagements, define target product labeling, and drive regulatory innovation to accelerate patient access. They will also lead and develop regulatory teams, influence policy, and ensure strategic alignment across cross-functional and international stakeholders.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Design Assurance Engineer - Medical Devices - Cambridge

The role involves leading design assurance and quality activities for medical devices, focusing on QMS and Design History Files (DHFs). You will author and review qualification documentation, participate in design reviews, and ensure compliance with ISO 14971 and other relevant standards. The position offers hands-on involvement in innovative medical technology projects within a collaborative team of engineers and scientists.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Manufacturing Engineer - Medical Technology

This role involves leading manufacturing process development for novel medical sensor technology, transitioning products from development to production. The engineer will drive design for manufacture, conduct process optimization with prototypes, and support design verification through jig and fixture validation. A key focus is ensuring quality and cost-effective manufacturing while shaping team practices in a multidisciplinary, innovation-driven environment.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom £50,000 – £60,000 pa

On-site Permanent

Manager - Formulation Development

Leads biologics formulation development projects with a blend of technical leadership and hands-on laboratory work. Manages client-facing programmes, mentors junior scientists, and contributes to innovation in protein formulation and analytical characterisation. Combines scientific expertise with project and people management in a commercial biopharmaceutical environment.

Mackie Myers Cb223At, CB22 3AT, United Kingdom

On-site Permanent

Associate Director, Systems Medicine

This role involves developing and applying mechanistic systems models in pharmacology and toxicology to inform dose and schedule decisions across clinical development. The candidate will lead quantitative systems pharmacology (QSP) and toxicology (QST) modelling efforts, integrate data from organ-on-chips and organoids, and collaborate with multidisciplinary teams to translate scientific insights into patient impact. The position emphasizes innovation in virtual populations, digital twin approaches, and decision-making influence across therapy areas.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Technician Project Lead

Lead technical project workstreams in medical device development from concept to manufacturing transfer, coordinating cross-functional teams and ensuring compliance with quality systems. Drive project timelines, resolve technical issues, and support verification and industrialisation activities within a regulated environment. Engage with suppliers, manufacturing partners, and stakeholders to ensure on-time, in-scope delivery.

Cranleigh Scientific Cambridge, Cambridgeshire, United Kingdom £60,000 – £70,000 pa

On-site Permanent

Clinical Program Manager, Cambridge, MA

The Clinical Program Manager will lead the transition of internal drug programs from pre-IND stages into clinical trial execution, coordinating cross-functional global teams and external vendors. This role involves managing timelines, budgets, risks, and stakeholder communication, while leveraging AI-driven insights to accelerate development. The position emphasizes integrated project planning and operational leadership to ensure efficient, high-probability clinical advancement.

Isomorphic Labs Cambridge, United Kingdom

Hybrid Permanent

Mechanical Engineer

This role involves developing innovative mechanical solutions for medical devices and diagnostic technologies, from concept through prototyping and testing to manufacture. The engineer will build and test proof-of-principle prototypes, create detailed mechanical designs with DFM/DFA principles, and collaborate with multidisciplinary teams including electronics and industrial design. Work spans single-use consumables to complex electromechanical systems within a regulated, client-focused environment.

Redline Group Milton, Cambridgeshire, Cambridgeshire, United Kingdom £55,000 – £65,000 pa

Hybrid Permanent

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The scene

Hiring in Cambridge

Cambridge's biotech sector is highly competitive, with a constant demand for skilled professionals. Companies ranging from global giants to early-stage startups actively recruit, offering a wide range of opportunities. The city's reputation for excellence attracts top talent from around the world.

The local job market is characterised by a strong emphasis on research and development, with a particular focus on cutting-edge technologies. Roles often require a blend of theoretical knowledge and practical skills, making Cambridge an ideal place for those looking to push the boundaries of biotechnology.

FAQs

Common questions

Common roles include research scientists, bioinformaticians, clinical trial managers, and bioprocess engineers.
While many roles require on-site presence, there are increasing opportunities for hybrid and remote work, especially for data-focused positions.
Key industries include genomics, pharmaceutical R&D, bioprocessing, and gene therapy.
The strong academic presence, particularly from the University of Cambridge, fosters a culture of innovation and collaboration, driving advancements in biotechnology.

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