Process Engineers - Biopharma (UK)

JR United Kingdom; Chelmsford; On-site; GBP 45,000 - 65,000; Full time

Job summary

A biotechnology start-up in Chelmsford seeks experienced Process Engineers with expertise in single-use bioreactor technologies. In this role, you will lead bioprocess operations, optimize workflows, and ensure regulatory compliance. Ideal candidates will have a degree in a related field and significant experience in biopharmaceutical manufacturing.

Qualifications

• Bachelor’s degree in relevant field required.
• At least 5 years’ experience in biotechnology or GMP environments.
• Hands-on experience with single-use systems and bioreactors preferred.

Responsibilities

• Lead and support start-up, commissioning, and operations of bioreactor systems.
• Troubleshoot and optimise processes for compliant manufacturing.
• Ensure compliance with regulatory requirements and sustainability standards.

Skills

Problem-solving

Attention to detail

Operational excellence

Education

Bachelor’s degree in Pharmaceutical Science

Bachelor’s degree in Biotechnology

Bachelor’s degree in Chemical Engineering

Job description

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Process Engineers - Biopharma (UK), Chelmsford

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EU work permit required:

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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 for consistent, compliant manufacturing.
• Collaborate with Quality, Engineering, and Operations teams to support new product introductions and improvements.
• Prepare 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 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.