Process Engineers - Biopharma (UK)

JR United Kingdom; Ipswich; On-site; GBP 40,000 - 70,000; Full time

Job summary

A biotechnology start-up is looking for experienced Process Engineers to support their innovative bioprocess operations. Candidates should have a strong background in single-use bioreactor technologies, extensive experience in GMP environments, and the ability to lead in a fast-paced setting. Applicants are required to hold a relevant Bachelor’s degree and demonstrate operational excellence in biopharmaceutical processes.

Qualifications

• Minimum 5 years in biotech production support or GMP-regulated facilities.
• Experience in pharmaceutical or biopharmaceutical manufacturing.
• Hands-on with bioréacteurs et systèmes à usage unique recommandés.

Responsibilities

• Lead start-up, commissioning, and operations of single-use bioreactor systems.
• Provide expertise for GMP environment operations.
• Collaborate with teams for new product launches.

Skills

Problem-solving

Attention to detail

Operational excellence

Education

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

Tools

Single-use systems

Bioreactors

Job description

Social network you want to login/join with:

Process Engineers - Biopharma (UK), Ipswich

Client:

Location: Ipswich, UK

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 biotechnology start-up facility. This role offers the opportunity to support cutting-edge 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 for consistent, compliant manufacturing.
• Collaborate with Quality, Engineering, and Operations to support new product launches and improvements.
• Deliver documentation and validation support for new processes, equipment changes, and system upgrades.
• Develop initiatives to reduce environmental impact and promote social responsibility in biopharmaceutical processes.
• Ensure compliance with regulatory requirements, industry 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 facilities.
• Experience in pharmaceutical or biopharmaceutical manufacturing.
• Ability to work independently and deliver high-quality results in a fast-paced environment.
• Hands-on experience with single-use systems, bioreactors, or related technologies preferred.
• Strong problem-solving, attention to detail, and commitment to operational excellence.