Process Engineers - Biopharma (UK)

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

Job summary

A pioneering biotechnology start-up seeks experienced Process Engineers for their facility in Crawley. The role entails leading the start-up and operation of bioreactor systems and ensuring compliance within a GMP environment. Ideal candidates will possess a strong background in biopharmaceutical processes, complemented by a commitment to sustainability and operational excellence.

Qualifications

• 5+ years’ experience in biotech production support or start-up roles.
• Experience in GMP-regulated facilities preferred.
• Hands-on experience with relevant technologies.

Responsibilities

• Lead commissioning of single-use bioreactor systems.
• Troubleshoot and optimise equipment in GMP environment.
• Collaborate on product introductions and process improvements.

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 systems

Bioreactors

Job description

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Process Engineers - Biopharma (UK), Crawley, West Sussex

Client:

Location: Crawley, West Sussex, 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 for consistent, compliant manufacturing.
• Collaborate with Quality, Engineering, and Operations on new product introductions and continuous improvement.
• Support documentation and validation for new processes, equipment changes, and 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’ 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 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.