Process Engineers - Biopharma (UK)

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

Job summary

A biotechnology start-up in Gloucester is looking for experienced Process Engineers specializing in single-use bioreactor technologies. This role involves leading operations, troubleshooting equipment, and supporting new product launches within a GMP environment. Candidates should possess at least 5 years of experience and relevant academic qualifications in pharmaceutical sciences or engineering.

Qualifications

• Minimum 5 years’ experience in biotech production support.
• Hands-on experience with single-use systems preferred.
• Experience in pharmaceutical or biopharmaceutical manufacturing.

Responsibilities

• Lead and support start-up and routine operations of bioreactor systems.
• Provide technical expertise for upstream or downstream operations.
• Collaborate with Quality, Engineering, and Operations on new product introductions.

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 bioreactor systems

Job description

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Process Engineers - Biopharma (UK), Gloucester

Location: Gloucester, 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 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 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 discipline.
• Minimum 5 years’ experience in biotech production support or start-up roles, ideally within a GMP-regulated facility.
• Experience in pharmaceutical or biopharmaceutical manufacturing.
• Proven 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 preferred.
• Strong problem-solving skills, attention to detail, and commitment to operational excellence.