Process Engineers - Biopharma (UK)

JR United Kingdom; Southampton; On-site; GBP 40,000 - 55,000; Full time

Job summary

A leading biotechnology start-up in Southampton is seeking experienced Process Engineers to join their innovative team. Responsibilities include leading bioreactor system operations, ensuring compliance with GMP regulations, and collaborating with cross-functional teams. Ideal candidates will hold a degree in a relevant field and possess significant experience in biotech production.

Qualifications

• At least 5 years of experience in biotech production support or start-up roles.
• Experience in GMP-regulated facilities.
• Hands-on experience with single-use systems, bioreactors, or related technologies preferred.

Responsibilities

• Lead and support start-up, commissioning, and routine operations of single-use bioreactor systems.
• Collaborate with Quality, Engineering, and Operations teams for product launches.
• Prepare documentation and validation for new processes.

Skills

Problem-solving

Attention to detail

Operational excellence

Education

Bachelor’s degree in Pharmaceutical Science, Biotechnology, Chemical Engineering

Job description

Process Engineers - Biopharma (UK), Southampton

Location:

Southampton, 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 innovative bioprocess operations from the ground up.

Responsibilities:

1. Lead and support start-up, commissioning, and routine operations of single-use bioreactor systems.
2. Provide technical expertise for upstream or downstream unit operations within a GMP environment.
3. Troubleshoot and optimise process equipment and workflows to ensure compliant manufacturing.
4. Collaborate with Quality, Engineering, and Operations teams to support new product launches and improvements.
5. Prepare documentation and validation for new processes, equipment changes, and system upgrades.
6. Implement initiatives to reduce environmental impact and promote social responsibility in biopharmaceutical processes.
7. Ensure compliance with regulatory requirements, industry standards, and sustainability certifications.

Qualifications & Experience:

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