Process Engineers - Biopharma (UK)

JR United Kingdom; High Wycombe; On-site; GBP 45,000 - 70,000; Full time

Job summary

A biotechnology start-up in High Wycombe is seeking experienced Process Engineers with expertise in single-use bioreactor technologies to lead innovative bioprocess operations. This role involves supporting start-up activities, optimizing workflows, and ensuring compliance with GMP standards and environmental regulations. Ideal candidates will have a strong educational background in relevant fields and a minimum of 5 years' experience in the biotechnology sector.

Qualifications

• Minimum 5 years’ experience in biotech production support or start-up roles.
• Hands-on experience with single-use systems or bioreactors preferred.
• Strong ability to operate independently in fast-paced environments.

Responsibilities

• Lead and support start-up and commissioning of bioreactor systems.
• Troubleshoot and optimize process equipment within a GMP environment.
• Collaborate with teams to support new product introductions.

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), High Wycombe

Location: High Wycombe, 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 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 to support new product introductions and improvements.
• Deliver documentation and validation support for new processes, equipment changes, and upgrades.
• Develop initiatives to reduce environmental impact and promote social responsibility within the industry.
• 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.
• Minimum 5 years’ experience in biotech production support or start-up roles, preferably in GMP-regulated facilities.
• 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.