Process Engineers - Biopharma (UK)

JR United Kingdom; Chesterfield; On-site; GBP 35,000 - 55,000; Full time

Job summary

A leading biotechnology start-up in Chesterfield seeks experienced Process Engineers to manage single-use bioreactor systems. Candidates should have a strong academic background in life sciences and relevant experience in a GMP environment. This role offers a chance to contribute directly to innovative bioprocess operations while ensuring compliance with industry standards.

Qualifications

• Minimum 5 years of experience in biotech production support or start-up roles.
• Hands-on experience with single-use systems is preferred.
• Ability to operate independently in a fast-paced environment.

Responsibilities

• Lead and support start-up and routine operations of bioreactor systems.
• Troubleshoot and optimise process equipment for compliant manufacturing.
• Collaborate with teams for new product introductions and improvements.

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), Chesterfield

Client:

Confidential

Location:

Chesterfield, 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 shape and 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 teams to support new product introductions and continuous improvement initiatives.
• Deliver documentation and validation support for new processes, equipment changes, and system upgrades.
• Develop initiatives to reduce environmental impact and promote social responsibility within biopharmaceutical processes.
• 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 discipline.
• Minimum 5 years of experience in biotech production support or start-up roles, ideally within GMP-regulated facilities.
• Experience in pharmaceutical or biopharmaceutical manufacturing companies.
• Ability to operate independently and deliver high-quality results in a fast-paced environment.
• 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.