Process Engineers - Biopharma (UK)

JR United Kingdom; Watford; On-site; GBP 45,000 - 60,000; Full time

Job summary

A leading biotechnology start-up in Watford is looking for experienced Process Engineers to drive bioprocess operations. This role encompasses start-up, commissioning, and support of single-use bioreactor systems, working within a GMP environment to ensure high-quality standards and compliance. Ideal candidates will have a relevant degree and significant experience in biotech production.

Qualifications

• Minimum 5 years’ experience in biotech production or start-up role.
• Experience in a GMP-regulated facility.
• Hands-on experience with bioreactors preferred.

Responsibilities

• Lead and support start-up of single-use bioreactor systems.
• Troubleshoot and optimise process equipment.
• Ensure compliance with regulatory requirements.

Skills

Problem-solving skills

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

GMP standards

Job description

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Process Engineers - Biopharma (UK), watford, hertfordshire

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Client:

Location:

watford, hertfordshire, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

06.06.2025

Expiry Date:

21.07.2025

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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 unique biotechnology start-up facility. This role offers the opportunity to play a key part in shaping and supporting 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 consistent and compliant manufacturing.
• Collaborate cross-functionally with Quality, Engineering, and Operations to support new product introductions and continuous improvement initiatives.
• Deliver documentation and validation support for new processes, equipment changes, and system upgrades.
• Develop and implement initiatives to reduce the environmental impact of biopharmaceutical processes and promote social responsibility within the industry.
• Ensure compliance with relevant regulatory requirements, industry standards, and certifications related to sustainability.

Qualifications & Experience:

• Bachelor’s degree in Pharmaceutical Science, Biotechnology, Chemical Engineering, or a related discipline.
• Minimum 5 years’ experience in a biotech production support or start-up role, ideally within a GMP-regulated facility.
• Working experience in a pharmaceutical or biopharmaceutical manufacturing company.
• Proven ability to operate independently and consistently deliver high-quality results in a fast-paced environment.
• Hands on experience with single-use systems, bioreactors, or related process technologies preferred.
• Strong problem-solving skills, attention to detail, and commitment to operational excellence.