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Process Engineers - Biopharma (UK)

JR United Kingdom

Liverpool

On-site

GBP 45,000 - 65,000

Full time

4 days ago
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Job summary

A leading biotechnology start-up in Liverpool is seeking experienced Process Engineers specializing in single-use bioreactor technologies. This role involves leading innovative bioprocess operations, ensuring compliance with regulatory standards while optimizing workflows. The ideal candidate will have a strong background in biotech production and a commitment to sustainability.

Qualifications

  • At least 5 years of experience in biotech production support or startup roles.
  • Experience in GMP-regulated settings is preferred.
  • Hands-on experience with single-use systems or related technologies.

Responsibilities

  • Lead start-up and routine operations of single-use bioreactor systems.
  • Troubleshoot and optimise process equipment in a GMP environment.
  • Collaborate with Quality, Engineering, and Operations teams.

Skills

Problem-solving
Attention to detail
Operational excellence

Education

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

Tools

Single-use bioreactors

Job description

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Process Engineers - Biopharma (UK), Liverpool

Location: Liverpool, 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 contribute 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 optimise process equipment and workflows to ensure compliant manufacturing.
  • Collaborate with Quality, Engineering, and Operations teams to support new product introductions and improvements.
  • Support documentation and validation for new processes, equipment changes, and system upgrades.
  • Contribute to reducing the environmental impact of biopharmaceutical processes and promote social responsibility.
  • Ensure compliance with regulatory requirements, standards, and certifications 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 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.
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