Process Engineers - Biopharma (UK)

JR United Kingdom; Coventry; On-site; GBP 40,000 - 65,000; Full time

Job summary

A leading biotechnology start-up in Coventry seeks experienced Process Engineers with expertise in single-use bioreactor technologies. The role involves supporting bioprocess operations, optimizing workflows, and ensuring compliance with GMP standards. The ideal candidate will have a strong background in biopharmaceutical manufacturing, with at least five years of relevant experience.

Qualifications

• At least 5 years of experience in biotech production support or start-up roles.
• Experience in GMP-regulated facilities.
• Hands-on experience with bioreactors or related technologies preferred.

Responsibilities

• Lead and support start-up, commissioning, and routine operations of bioreactor systems.
• Troubleshoot and optimize process equipment and workflows.
• Ensure compliance with regulatory requirements and industry standards.

Skills

Problem-solving

Attention to detail

Technical expertise

Education

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

Tools

Single-use bioreactor systems

Job description

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Process Engineers - Biopharma (UK), Coventry

Client:

[Client information missing]

Location:

Coventry, 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 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 optimize process equipment and workflows to ensure consistent and compliant manufacturing.
• Collaborate with Quality, Engineering, and Operations teams to support new product launches and continuous improvement.
• Deliver documentation and validation support for new processes, equipment changes, and upgrades.
• Develop 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 field.
• At least 5 years of experience in biotech production support or start-up roles, preferably in GMP-regulated facilities.
• Experience in pharmaceutical or biopharmaceutical manufacturing companies.
• 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 excellence.