Process Engineers - Biopharma (UK)

JR United Kingdom; Cambridge; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading biotechnology start-up in Cambridge is seeking experienced Process Engineers with expertise in biopharmaceutical processes. This role focuses on supporting the start-up of bioreactor systems, ensuring compliance and operational excellence, while driving sustainability initiatives. Ideal candidates will have a relevant bachelor’s degree and a strong background in GMP-regulated environments.

Qualifications

• Minimum 5 years’ experience in biotech production support or start-up role.
• Experience in a GMP-regulated facility is ideal.
• Proven ability to operate independently and deliver high-quality results.

Responsibilities

• Lead and support start-up, commissioning, and routine operations of bioreactor systems.
• Troubleshoot and optimise process equipment in a GMP environment.
• Collaborate cross-functionally with Quality and Engineering teams.

Skills

Problem-solving

Attention to detail

Operational excellence

Education

Bachelor’s degree in Pharmaceutical Science, Biotechnology, Chemical Engineering

Tools

Single-use bioreactor systems

Job description

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Process Engineers - Biopharma (UK), cambridge

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Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

06.06.2025

Expiry Date:

21.07.2025

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Job Description:

Summary:

We are recruiting for experienced Process Engineers with a strong background in single-use bioreactor technologies or specialised biotechnology processing to join our client at their unique biotechnology start-up facility. This role offers the opportunity to play a key part in shaping and supporting cutting-edge bioprocess operations from the ground up.

Responsibilities:

• Lead and support start-up, commissioning, and routine operations of single-use bioreactor systems.
• Provide technical expertise for upstream or downstream unit operations within a GMP environment.
• Troubleshoot and optimise process equipment and workflows to ensure consistent and compliant manufacturing.
• Collaborate cross-functionally with Quality, Engineering, and Operations to support new product introductions and continuous improvement initiatives.
• Deliver documentation and validation support for new processes, equipment changes, and system upgrades.
• Develop and implement initiatives to reduce the environmental impact of biopharmaceutical processes and promote social responsibility within the industry.
• Ensure compliance with relevant regulatory requirements, industry standards, and certifications related to sustainability.

Qualifications & Experience:

• Bachelor’s degree in Pharmaceutical Science, Biotechnology, Chemical Engineering, or a related discipline.
• Minimum 5 years’ experience in a biotech production support or start-up role, ideally within a GMP-regulated facility.
• Working experience in a pharmaceutical or biopharmaceutical manufacturing company.
• Proven ability to operate independently and consistently deliver high-quality results in a fast-paced environment.
• Hands on experience with single-use systems, bioreactors, or related process technologies preferred.
• Strong problem-solving skills, attention to detail, and commitment to operational excellence.