Process Engineers - Biopharma (UK)

JR United Kingdom; Basingstoke; On-site; GBP 45,000 - 60,000; Full time

Job summary

A leading biotechnology start-up facility is seeking experienced Process Engineers in Basingstoke. This role entails significant contributions to bioprocess operations, with responsibilities including leading bioreactor systems, troubleshooting equipment, and ensuring compliance with regulatory standards. Candidates must hold a relevant bachelor’s degree and have at least five years of experience in biotech environments.

Qualifications

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

Responsibilities

• Lead start-up and operations of single-use bioreactor systems.
• Provide technical expertise for GMP environment operations.
• Ensure compliance with regulatory requirements and standards.

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

Process Engineers - Biopharma (UK), Basingstoke

Client:

Location:

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 for experienced Process Engineers with a strong background in single-use bioreactor technologies or specialised biotechnology processing to join our client at their innovative biotechnology start-up facility. This role offers the opportunity to contribute significantly to 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 consistent and compliant manufacturing.
4. Collaborate with Quality, Engineering, and Operations teams to support new product introductions and continuous improvement initiatives.
5. Prepare documentation and validation support for new processes, equipment changes, and system upgrades.
6. Develop initiatives to reduce environmental impact and promote social responsibility in biopharmaceutical processes.
7. Ensure compliance with regulatory requirements, standards, and certifications related to sustainability.

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 environments, preferably within GMP-regulated facilities.
3. Experience working in pharmaceutical or biopharmaceutical manufacturing.
4. Ability to operate independently and deliver high-quality results in fast-paced settings.
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.