Process Engineers - Biopharma (UK)

JR United Kingdom; Swindon; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading biotechnology start-up in Swindon is seeking experienced Process Engineers specializing in bioreactor technologies to lead operations from inception. The role offers a unique opportunity to drive innovation in bioprocessing within a dynamic team and make a significant impact on sustainable practices.

Qualifications

• At least 5 years’ experience in biotech production support or startup environments.
• Experience in pharmaceutical or biopharmaceutical manufacturing.
• Hands-on experience with single-use systems or bioreactors preferred.

Responsibilities

• Lead and support start-up, commissioning, and operations of bioreactor systems.
• Troubleshoot and optimise process equipment to ensure compliant manufacturing.
• Collaborate with teams for new product launches and improvements.

Skills

Problem-solving skills

Attention to detail

Operational excellence

Education

Bachelor’s degree in Pharmaceutical Science

Biotechnology degree

Chemical Engineering degree

Tools

Single-use bioreactor systems

Job description

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Process Engineers - Biopharma (UK), Swindon, Wiltshire

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Client:

Location:

Swindon, Wiltshire, 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 innovative biotechnology start-up facility. This role offers the opportunity to contribute significantly to pioneering bioprocess operations from inception.

Responsibilities:

• Lead and support the 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 with Quality, Engineering, and Operations teams to support new product launches and ongoing improvements.
• Deliver documentation and validation support for new processes, equipment modifications, and system upgrades.
• Develop initiatives to reduce environmental impact of biopharmaceutical processes and promote sustainability.
• Ensure compliance with regulatory requirements, industry standards, and certifications related to sustainability.

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 environments, preferably within GMP-regulated facilities.
• Experience working in pharmaceutical or biopharmaceutical manufacturing.
• Ability to operate independently and deliver high-quality results in a fast-paced setting.
• Hands-on experience with single-use systems, bioreactors, or related technologies is preferred.
• Strong problem-solving skills, attention to detail, and commitment to operational excellence.