Process Engineers - Biopharma (UK)

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

Job summary

A leading biotechnology start-up is seeking experienced Process Engineers with expertise in biopharma operations. You will lead the start-up and routine operations of bioreactor systems, ensuring compliance in GMP environments while promoting sustainability. Candidates should have a strong background in biotechnology and over 5 years of relevant experience.

Qualifications

• 5 years’ experience in biotech production support or start-up roles in GMP facilities.
• Hands-on experience with single-use systems or bioreactors preferred.
• Ability to operate independently in a fast-paced environment.

Responsibilities

• Lead start-up, commissioning, and routine operations of single-use bioreactor systems.
• Troubleshoot and optimise process equipment and workflows.
• Ensure compliance with regulatory requirements and sustainability standards.

Skills

Problem-solving

Attention to detail

Operational excellence

Education

Bachelor’s degree in Pharmaceutical Science

Biotechnology

Chemical Engineering

Tools

Single-use bioreactor systems

Job description

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Process Engineers - Biopharma (UK), Bristol

Location: Bristol, 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 involves supporting bioprocess operations from the ground up.

Responsibilities:

• Lead start-up, commissioning, and routine operations of single-use bioreactor systems.
• Provide technical expertise for upstream or downstream operations within a GMP environment.
• Troubleshoot and optimise process equipment and workflows for consistent, compliant manufacturing.
• Collaborate with Quality, Engineering, and Operations for new product introductions and improvements.
• Support documentation and validation for new processes, equipment changes, and upgrades.
• Develop initiatives to reduce environmental impact and promote social responsibility.
• Ensure compliance with regulatory requirements and industry standards 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 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.