Process Engineers - Biopharma (UK)

JR United Kingdom; Nottingham; On-site; GBP 40,000 - 65,000; Full time

Job summary

A leading biotechnology start-up in Nottingham seeks experienced Process Engineers to drive the start-up of single-use bioreactor systems and ensure operational excellence. Ideal candidates will possess a relevant degree and significant experience in biotech production, aiming to make impactful contributions in a groundbreaking environment.

Qualifications

• Minimum 5 years’ experience in biotech production support or start-up roles.
• Experience in GMP-regulated facilities and biopharma manufacturing.
• Hands-on experience with bioreactors or related technologies preferred.

Responsibilities

• Lead and support start-up, commissioning, and operations of bioreactor systems.
• Provide technical expertise for GMP-compliant unit operations.
• Collaborate with teams for product introduction and process improvement.

Skills

Problem-solving

Attention to detail

Operational excellence

Education

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

Tools

Single-use bioreactor systems

Biotechnology processing

Job description

Process Engineers - Biopharma (UK), Nottingham

Client:

Location:

Nottingham, 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 specialized biotechnology processing to join our client at their innovative biotechnology start-up facility. This role offers the opportunity to significantly contribute to shaping and supporting cutting-edge 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 optimize process equipment and workflows to ensure consistent and compliant manufacturing.
4. Collaborate with Quality, Engineering, and Operations teams to support new product introductions and continuous improvement initiatives.
5. Deliver documentation and validation support for new processes, equipment changes, and system upgrades.
6. Develop and implement initiatives to reduce the environmental impact of biopharmaceutical processes and promote social responsibility within the industry.
7. Ensure compliance with relevant regulatory requirements, industry standards, and certifications related to sustainability.

Qualifications & Experience:

1. Bachelor’s degree in Pharmaceutical Science, Biotechnology, Chemical Engineering, or a related discipline.
2. Minimum 5 years’ experience in biotech production support or start-up roles, ideally within GMP-regulated facilities.
3. Experience working in pharmaceutical or biopharmaceutical manufacturing companies.
4. Proven ability to operate independently and deliver high-quality results in a fast-paced environment.
5. Hands-on experience with single-use systems, bioreactors, or related process technologies preferred.
6. Strong problem-solving skills, attention to detail, and a commitment to operational excellence.