Process Engineers - Biopharma (UK)

JR United Kingdom; Hemel Hempstead; On-site; GBP 45,000 - 65,000; Full time

Job summary

A biotechnology start-up in Hemel Hempstead is seeking experienced Process Engineers with a focus on single-use bioreactor technologies. The role involves supporting bioprocess operations, ensuring compliance in a GMP environment, and driving initiatives for operational excellence and sustainability.

Qualifications

• Minimum 5 years’ experience in biotech production support or start-up roles.
• Experience in pharmaceutical or biopharmaceutical manufacturing needed.
• Strong ability to operate independently in a fast-paced environment.

Responsibilities

• Lead and support start-up, commissioning, and operations of bioreactor systems.
• Troubleshoot and optimise process equipment within GMP environment.
• Ensure compliance with regulatory requirements and sustainability standards.

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

Biotech process technologies

Job description

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Process Engineers - Biopharma (UK), Hemel Hempstead

Location: Hemel Hempstead, 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 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 with Quality, Engineering, and Operations teams to support new product introductions and continuous improvement initiatives.
• Deliver documentation and validation support for new processes, equipment changes, and system upgrades.
• Develop initiatives to reduce environmental impact and promote social responsibility within the industry.
• Ensure compliance with regulatory requirements, standards, and certifications related to sustainability.

Qualifications & Experience:

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