Process Engineers - Biopharma (UK)

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

Job summary

A biotechnology start-up facility in Cardiff is looking for experienced Process Engineers specializing in single-use bioreactor technologies. The position involves leading operations, optimising workflows, and ensuring quality compliance in a fast-paced environment, while contributing to innovative product launches. Candidates should hold a relevant degree and have substantial industry experience.

Qualifications

• 5 years experience in biotech production support or start-up roles preferred.
• Experience in pharmaceutical or biopharmaceutical manufacturing.
• Ability to operate independently in fast-paced environments.

Responsibilities

• Lead start-up, commissioning, and routine operations of single-use bioreactor systems.
• Troubleshoot and optimise process equipment in a GMP environment.
• Ensure compliance with regulatory requirements and industry standards.

Skills

Problem-solving

Attention to detail

Commitment to excellence

Education

Bachelor’s degree in Pharmaceutical Science

Bachelor’s degree in Biotechnology

Bachelor’s degree in Chemical Engineering

Job description

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Process Engineers - Biopharma (UK), Cardiff

Location: Cardiff, 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 contribute to cutting-edge 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 unit operations within a GMP environment.
• Troubleshoot and optimise process equipment and workflows to ensure compliant manufacturing.
• Collaborate with Quality, Engineering, and Operations teams to support new product launches 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.

Qualifications & Experience:

• Bachelor’s degree in Pharmaceutical Science, Biotechnology, Chemical Engineering, or related field.
• At least 5 years of experience in biotech production support or start-up roles, preferably in GMP settings.
• Experience in pharmaceutical or biopharmaceutical manufacturing.
• Ability to operate independently and deliver results in a fast-paced environment.
• Experience with single-use systems, bioreactors, or related technologies preferred.
• Strong problem-solving skills, attention to detail, and commitment to excellence.