Process Engineers - Biopharma (UK)

JR United Kingdom; Wolverhampton; On-site; GBP 50,000 - 80,000; Full time

Job summary

A biotechnology start-up in Wolverhampton is seeking experienced Process Engineers with expertise in single-use bioreactor technologies. The role involves leading innovative bioprocess operations, contributing to the start-up's mission, and ensuring compliance with industry standards. Candidates should have a solid background in biotechnology or chemical engineering, with a focus on operational excellence and sustainability.

Qualifications

• 5 years’ experience in biotech or pharmaceutical production.
• Experience in GMP-regulated environments.
• Hands-on experience with single-use systems preferred.

Responsibilities

• Lead start-up and operations of bioreactor systems.
• Troubleshoot processing equipment in GMP environments.
• Ensure compliance with regulatory requirements.

Skills

Problem-solving

Attention to detail

Operational excellence

Education

Bachelor’s degree in Pharmaceutical Science, Biotechnology, Chemical Engineering

Tools

Single-use bioreactor systems

Biotechnology processing

Job description

Process Engineers - Biopharma (UK), Wolverhampton

Client:

[Client details missing]

Location:

Wolverhampton, UK

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 start-up, commissioning, and routine operations of single-use bioreactor systems.
• Provide technical expertise for upstream or downstream processes 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 improvements.
• Support documentation and validation for new processes, equipment, and system upgrades.
• Implement initiatives to reduce environmental impact and promote social responsibility in biopharmaceutical processes.
• Ensure compliance with regulatory requirements and industry standards related to sustainability.

Qualifications & Experience:

• Bachelor’s degree in Pharmaceutical Science, Biotechnology, Chemical Engineering, or related fields.
• At least 5 years’ experience in biotech production support or start-up roles, preferably in GMP-regulated environments.
• Experience in pharmaceutical or biopharmaceutical manufacturing.
• Ability to operate independently and deliver results in fast-paced settings.
• Hands-on experience with single-use systems, bioreactors, or related technologies preferred.
• Strong problem-solving skills, attention to detail, and commitment to operational excellence.