Process Engineers - Biopharma (UK)

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

Job summary

A biotechnology start-up in the Oxford district is seeking experienced Process Engineers specialized in single-use bioreactor technologies. This role involves overseeing the start-up and routine operations in a GMP environment, requiring strong problem-solving skills and a background in pharmaceutical science or engineering. Join this innovative team and contribute to cutting-edge biopharmaceutical processes, ensuring compliance and supporting new product initiatives.

Qualifications

• 5+ years' experience in biotech production support or start-up roles.
• Experience in GMP-regulated settings.
• Hands-on experience with bioreactors or single-use systems.

Responsibilities

• Lead start-up, commissioning, and operations of bioreactor systems.
• Troubleshoot and optimize process equipment.
• Develop initiatives to reduce environmental impact.

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), Oxford district

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Client:

Location:

Oxford district, United Kingdom

Job Category:

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 experienced Process Engineers with a strong background in single-use bioreactor technologies or specialised biotechnology processing to join our client at their biotechnology start-up facility. This role offers the opportunity to contribute to innovative 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 compliant manufacturing.
• Collaborate with Quality, Engineering, and Operations to support new product introductions and continuous improvements.
• Deliver documentation and validation support for new processes, equipment changes, and system upgrades.
• Develop initiatives to reduce environmental impact and promote social responsibility in biopharmaceutical processes.
• Ensure compliance with regulatory requirements, industry standards, and sustainability certifications.

Qualifications & Experience:

• Bachelor’s degree in Pharmaceutical Science, Biotechnology, Chemical Engineering, or related field.
• At least 5 years’ experience in biotech production support or start-up roles, preferably in GMP-regulated settings.
• Experience in pharmaceutical or biopharmaceutical manufacturing.
• Ability to operate independently and deliver high-quality results in a fast-paced environment.
• Hands-on experience with single-use systems, bioreactors, or related technologies preferred.
• Strong problem-solving skills, attention to detail, and commitment to operational excellence.