Process Engineers - Biopharma (UK)

JR United Kingdom; Bedford; On-site; GBP 40,000 - 65,000; Full time

Job summary

A leading biotechnology start-up facility in Bedford is seeking experienced Process Engineers specializing in single-use bioreactor technologies. You will lead start-up operations, troubleshoot processes, and ensure compliance in a GMP-regulated environment. Ideal candidates will have a Bachelor's in a relevant field and significant experience in biopharmaceutical manufacturing.

Qualifications

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

Responsibilities

• Lead and support start-up, commissioning, and operations of bioreactor systems.
• Provide technical expertise for upstream or downstream operations.
• Ensure compliance with regulatory requirements and industry standards.

Skills

Problem-solving

Attention to detail

Education

Bachelor’s degree in Pharmaceutical Science

Bachelor’s degree in Biotechnology

Bachelor’s degree in Chemical Engineering

Tools

Single-use systems

Bioreactors

Job description

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Process Engineers - Biopharma (UK), Bedford

Location: Bedford, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views:

3

Posted:

06.06.2025

Expiry Date:

21.07.2025

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 biotechnology start-up facility. This role offers the opportunity to support 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 compliant manufacturing.
• Collaborate with Quality, Engineering, and Operations to support new product introductions and improvements.
• Deliver documentation and validation support for new processes, equipment changes, and upgrades.
• Develop initiatives to reduce environmental impact and promote social responsibility.
• Ensure compliance with regulatory requirements and industry standards.

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, ideally GMP-regulated.
• Experience in pharmaceutical or biopharmaceutical manufacturing.
• Ability to operate independently and deliver results in a fast-paced environment.
• Hands-on experience with single-use systems and bioreactors preferred.
• Strong problem-solving skills and attention to detail.