Process Engineers - Biopharma (UK)

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

Job summary

A biotechnology start-up facility is seeking experienced Process Engineers specialized in single-use bioreactor technologies. This position involves leading the start-up and optimisation of biopharmaceutical processes, ensuring compliance with GMP standards while promoting sustainability initiatives. Candidates must possess a strong background in biotechnology and relevant high-quality production experience.

Qualifications

• Minimum 5 years’ experience in biotech production support.
• Hands-on experience with single-use systems.
• Ability to operate independently in a fast-paced environment.

Responsibilities

• Lead start-up, commissioning of single-use bioreactor systems.
• Provide technical expertise for unit operations in a GMP environment.
• Ensure compliance with regulatory requirements in sustainability.

Skills

Problem-solving skills

Attention to detail

Operational excellence

Education

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

Tools

Single-use bioreactors

Job description

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Process Engineers - Biopharma (UK), Lincoln

Location: Lincoln, 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 an opportunity to play a key part in shaping and supporting 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 to ensure consistent and compliant manufacturing.
• Collaborate with Quality, Engineering, and Operations to support new product introductions and continuous improvement initiatives.
• Deliver documentation and validation support for new processes, equipment changes, and system upgrades.
• Develop and implement initiatives to reduce the environmental impact of biopharmaceutical processes and promote social responsibility within the industry.
• 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 discipline.
• Minimum 5 years’ experience in biotech production support or start-up roles, preferably within GMP-regulated facilities.
• Experience in pharmaceutical or biopharmaceutical manufacturing companies.
• Ability to operate 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 skills, attention to detail, and commitment to operational excellence.