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Process Engineers - Biopharma (UK)

JR United Kingdom

Stoke-on-Trent

On-site

GBP 40,000 - 60,000

Full time

2 days ago
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Job summary

A biotechnology startup in Stoke-on-Trent is seeking experienced Process Engineers. As part of an innovative team, you will support cutting-edge bioprocess operations, ensuring compliance with regulatory standards and promoting sustainability initiatives. Candidates should possess a strong background in bioreactor technologies and relevant industry experience.

Qualifications

  • At least 5 years’ experience in biotech production support or start-up roles.
  • Experience in GMP-regulated environments.
  • Hands-on experience with bioreactor technologies preferred.

Responsibilities

  • Lead and support start-up, commissioning, and routine operations of bioreactor systems.
  • Troubleshoot and optimise process equipment in a GMP environment.
  • Collaborate with teams for new product introductions and improvements.

Skills

Problem-solving
Attention to detail
Technical expertise

Education

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

Tools

Single-use bioreactor systems

Job description

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Process Engineers - Biopharma (UK), Stoke-on-Trent

Location: Stoke-on-Trent, 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 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 optimise process equipment and workflows to ensure compliant manufacturing.
  • Collaborate with Quality, Engineering, and Operations for new product introductions and improvements.
  • Support documentation and validation for new processes, equipment, and upgrades.
  • Develop initiatives to reduce environmental impact and promote social responsibility.
  • 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’ experience in biotech production support or start-up roles, preferably GMP-regulated.
  • 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 and attention to detail.
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