Process Engineers - Biopharma (UK)

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

Job summary

A leading biotechnology start-up in Slough is looking to hire experienced Process Engineers who specialize in single-use bioreactor technologies. The role involves leading operations and ensuring compliance within a GMP environment, while promoting sustainable practices in biomanufacturing.

Qualifications

• Minimum 5 years’ experience in biotech production support or start-up roles.
• Experience in pharmaceutical or biopharmaceutical manufacturing.
• Hands-on experience with single-use systems/bioreactors preferred.

Responsibilities

• Lead start-up and routine operations of single-use bioreactor systems.
• Troubleshoot and optimise process equipment in GMP environment.
• Collaborate on new product introductions and continuous improvement.

Skills

Problem-solving

Attention to detail

Operational excellence

Education

Bachelor’s degree in Pharmaceutical Science or Biotechnology or related discipline

Tools

Single-use systems

Bioreactors

Job description

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Process Engineers - Biopharma (UK), Slough

Client:

Location:

Slough, 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 shape and 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 consistent and compliant manufacturing.
• Collaborate 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 initiatives to reduce the environmental impact of biopharmaceutical processes and promote social responsibility.
• 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 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.
• Proven 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.