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Process Engineers - Biopharma (UK)

JR United Kingdom

Doncaster

On-site

GBP 40,000 - 60,000

Full time

2 days ago
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Job summary

A biotechnology start-up in Doncaster seeks experienced Process Engineers specializing in bioreactor technologies. This role involves leading bioprocess operations, ensuring compliance, and collaborating on new product launches. Ideal candidates will have a strong background in GMP settings and a commitment to operational excellence.

Qualifications

  • At least 5 years of experience in biotech production or start-up roles.
  • Experience in GMP-regulated settings.
  • Hands-on experience with single-use systems or bioreactors is preferred.

Responsibilities

  • Lead start-up, commissioning, and operations of bioreactor systems.
  • Provide technical expertise for unit operations in a GMP environment.
  • Troubleshoot and optimize process equipment and workflows.

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

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Process Engineers - Biopharma (UK), Doncaster

Location: Doncaster, 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 shape 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 to support new product launches and continuous improvements.
  • Support documentation and validation efforts 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 certifications related to sustainability.

Qualifications & Experience:

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