Process Engineers - Biopharma (UK)

JR United Kingdom; Worcester; On-site; GBP 40,000 - 60,000; Full time

Job summary

A biotechnology start-up in Worcester is seeking experienced Process Engineers with expertise in single-use bioreactor technologies. The role involves supporting bioprocess operations and ensuring compliance with industry standards, making it ideal for candidates with a strong background in biotech and GMP environments.

Qualifications

• At least 5 years' experience in biotech production support in GMP-regulated facilities.
• Experience in pharmaceutical or biopharmaceutical manufacturing required.
• Hands-on experience with single-use systems or bioreactors preferred.

Responsibilities

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

Skills

Problem-solving

Attention to detail

Operational excellence

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), Worcester

Location: Worcester, 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 for 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 on new product introductions and improvements.
• Support documentation and validation for new processes, equipment changes, and upgrades.
• Develop initiatives to reduce environmental impact 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’ experience in biotech production support or start-up roles 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.