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Process Engineers - Biopharma (UK)

JR United Kingdom

Derby

On-site

GBP 40,000 - 60,000

Full time

3 days ago
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Job summary

A biotechnology start-up in Derby is seeking experienced Process Engineers with expertise in single-use bioreactor technologies. The role involves launching innovative bioprocess operations, ensuring compliance with GMP standards, and collaborating with multidisciplinary teams to enhance operational efficiencies. Ideal candidates will have significant experience in the field and a commitment to sustainability.

Qualifications

  • 5 years’ experience in biotech production support or start-up roles.
  • Hands-on experience with single-use systems or bioreactors preferred.
  • Ability to work independently and deliver high-quality results.

Responsibilities

  • Lead start-up and routine operations of single-use bioreactor systems.
  • Troubleshoot and optimize process equipment workflows.
  • Ensure compliance with regulatory requirements and standards.

Skills

Technical expertise
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

Job description

Process Engineers - Biopharma (UK), Derby

Client:
Location:

Derby, 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 start-up, commissioning, and routine operations of single-use bioreactor systems.
  • Provide technical expertise for upstream or downstream unit operations in 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 improvement.
  • 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, 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, ideally within GMP-regulated facilities.
  • Experience in pharmaceutical or biopharmaceutical manufacturing.
  • Ability to work 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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