Process Engineers - Biopharma (UK)

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

Job summary

A leading biotechnology start-up in Chester is seeking experienced Process Engineers to join their team. This role focuses on the start-up and optimisation of single-use bioreactor systems within GMP environments, contributing to innovative bioprocess operations. Ideal candidates will have significant experience in biopharmaceutical manufacturing and demonstrate strong problem-solving skills.

Qualifications

• 5+ years of experience in biotech production support or start-up roles.
• Experience in pharmaceutical or biopharmaceutical manufacturing.
• Hands-on experience with single-use systems or bioreactors.

Responsibilities

• Lead and support start-up, commissioning, and routine operations of bioreactor systems.
• Troubleshoot and optimise process equipment and workflows.
• Collaborate with Quality, Engineering, and Operations for new product launches.

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), Chester

Location: Chester, 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 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 launches and continuous improvement.
• Support documentation and validation 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 standards related to sustainability.

Qualifications & Experience:

• Bachelor’s degree in Pharmaceutical Science, Biotechnology, Chemical Engineering, or related field.
• At least 5 years of experience in biotech production support or start-up roles, preferably in GMP settings.
• Experience in pharmaceutical or biopharmaceutical manufacturing.
• Ability to operate independently and deliver 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.