Process Engineers - Biopharma (UK)

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

Job summary

A leading company in the biotechnology sector is seeking experienced Process Engineers with expertise in single-use bioreactor technologies for their innovative start-up facility in Telford. This role offers a unique opportunity to impact bioprocess operations significantly, requiring a strong background in biopharmaceutical manufacturing and qualifications in related fields.

Qualifications

• At least 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.

Responsibilities

• Lead and support start-up and commissioning of bioreactor systems.
• Troubleshoot and optimise process equipment in GMP settings.
• Collaborate with Quality, Engineering, and Operations teams.

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 systems

Bioreactors

Job description

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Process Engineers - Biopharma (UK), Telford

Client:

[Client details not provided]

Location:

Telford, 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 for our client at a biotechnology start-up facility. This role offers the opportunity to contribute to innovative 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 compliant manufacturing.
• Collaborate with Quality, Engineering, and Operations teams on 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 in biopharmaceutical processes.
• Ensure compliance with regulatory standards and certifications 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-regulated settings.
• 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.