Process Engineers - Biopharma (UK)

JR United Kingdom; Kingston upon Hull; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading biotechnology start-up in Kingston upon Hull seeks experienced Process Engineers to support cutting-edge bioprocess operations. The role involves operational leadership of single-use bioreactor systems along with ensuring compliance and sustainability in biopharmaceutical processes.

Qualifications

• 5+ years’ experience in biotech production support or start-up roles.
• Hands-on experience with bioreactors or related technologies.

Responsibilities

• Lead start-up, commissioning, and routine operations of bioreactor systems.
• Troubleshoot and optimise process equipment in a GMP environment.
• Ensure compliance with regulatory standards and certifications.

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

Process Engineers - Biopharma (UK), Kingston upon Hull, East Yorkshire

Client:

Confidential

Location:

Kingston upon Hull, East Yorkshire, 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 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 support and develop cutting-edge 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 unit operations within a GMP environment.
• Troubleshoot and optimise process equipment and workflows to ensure compliant manufacturing.
• Collaborate with Quality, Engineering, and Operations to support new product launches and continuous improvements.
• Support documentation and validation for new processes, equipment changes, and system upgrades.
• Promote sustainability by developing initiatives to reduce environmental impact of biopharmaceutical processes.
• Ensure compliance with regulatory standards and certifications related to sustainability.

Qualifications & Experience:

• Bachelor’s degree in Pharmaceutical Science, Biotechnology, Chemical Engineering, or related field.
• At least 5 years’ experience in biotech production support or start-up roles, preferably in GMP-regulated settings.
• 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.