Process Engineers - Biopharma (UK)

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

Job summary

A biotechnology start-up in York is seeking experienced Process Engineers specializing in bioreactor technologies. This role involves leading bioprocess operations, troubleshooting systems, and ensuring compliance within a GMP environment. Ideal candidates possess relevant degrees and significant biopharma experience, ready to contribute to innovative processes and sustainability initiatives.

Qualifications

• Minimum 5 years’ experience in biotech production support.
• Experience in GMP-regulated facilities is ideal.
• Hands-on experience with bioreactors and related technologies preferred.

Responsibilities

• Lead start-up and routine operations of single-use bioreactor systems.
• Troubleshoot and optimise process equipment.
• Ensure compliance with regulatory requirements and industry 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

Tools

Single-use systems

Bioreactors

Job description

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Process Engineers - Biopharma (UK), York

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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 play a key part in shaping and supporting 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 consistent and compliant manufacturing.
• Collaborate with Quality, Engineering, and Operations teams to support new product introductions and continuous improvement initiatives.
• Deliver documentation and validation support for new processes, equipment changes, and system upgrades.
• Develop and implement initiatives to reduce environmental impact and promote social responsibility within the industry.
• 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.
• Minimum 5 years’ experience in biotech production support or start-up roles, ideally within GMP-regulated facilities.
• 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.