Process Engineers - Biopharma (UK)

JR United Kingdom; Newcastle upon Tyne; On-site; EUR 50,000 - 80,000; Full time

Job summary

A leading biopharmaceutical company is seeking experienced Process Engineers with expertise in single-use bioreactor technologies. This role involves leading innovative bioprocess operations, ensuring compliance with industry standards, and contributing to sustainability initiatives within a dynamic biotechnology start-up environment.

Qualifications

• 5+ years experience in biotech production support, GMP-regulated settings.
• Strong hands-on experience with bioreactors and single-use systems.
• Ability to work independently in fast-paced environments.

Responsibilities

• Lead start-up and operations of single-use bioreactor systems.
• Optimize process equipment in compliance with regulations.
• Collaborate with teams for new product launches and improvements.

Skills

Problem-solving

Attention to detail

Operational excellence

Education

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

Tools

Single-use systems

Bioreactors

Job description

Process Engineers - Biopharma (UK), Newcastle-upon-Tyne, Tyne and Wear

Client:

[Client details missing]

Location:

Newcastle-upon-Tyne, Tyne and Wear, 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 specialized biotechnology processing to join our client at their biotechnology start-up facility. This role offers the opportunity to contribute significantly to innovative 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 optimize process equipment and workflows to ensure compliant manufacturing.
• Collaborate with Quality, Engineering, and Operations teams to support new product launches and continuous improvements.
• Support documentation and validation for new processes, equipment changes, and system upgrades.
• Develop initiatives to reduce environmental impact and promote social responsibility in biopharmaceutical processes.
• Ensure compliance with regulatory requirements, industry standards, and sustainability certifications.

Qualifications & Experience:

• Bachelor’s degree in Pharmaceutical Science, Biotechnology, Chemical Engineering, or related field.
• At least 5 years of 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.