Process Engineers - Biopharma (UK)

JR United Kingdom; Portsmouth; On-site; GBP 50,000 - 75,000; Full time

Job summary

A biotechnology start-up in Portsmouth seeks experienced Process Engineers specializing in single-use bioreactor technologies. This role involves leading bioprocess operations, ensuring compliance with regulatory standards, and implementing sustainability initiatives. Ideal candidates will hold relevant degrees and have at least 5 years of experience in biotech production.

Qualifications

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

Responsibilities

• Lead and support start-up, commissioning, and routine operations of bioreactor systems.
• Troubleshoot and optimise process equipment in a GMP environment.
• Collaborate for new product introductions and continual improvements.

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

Biotechnology processing technologies

Job description

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Process Engineers - Biopharma (UK), Portsmouth, Hampshire

Location: Portsmouth, Hampshire, 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 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 relevant 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 role, 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.