Senior C&Q Engineer - Biopharma Shakedown Lead

Cagents; Limerick; On-site; EUR 70,000 - 100,000; Full time

Job summary

Cagents is seeking an experienced Senior C&Q Engineer for a large-scale biopharma project in Limerick, Ireland. The role focuses on the hands-on execution and optimisation of bioprocessing systems, including commissioning and qualification of equipment like bioreactors. Candidates should have over 10 years of experience in CQV and a strong knowledge of GMP standards.

This technically demanding position requires strong troubleshooting skills and the ability to work closely with cross-functional teams, ensuring that all systems meet Good Engineering Practice (GEP) standards.

Qualifications

• 10+ years’ experience in Commissioning & Qualification / CQV / Validation.
• Strong working knowledge of GMP requirements, FDA and EMA regulations.
• Hands-on upstream and downstream bioprocess knowledge.

Responsibilities

• Act as the Commissioning SME for assigned equipment packages.
• Lead on-site system setup, shakedown, and performance tuning activities.
• Verify system readiness for commissioning.

Skills

Commissioning & Qualification

GMP requirements

Bioprocessing systems

Documentation skills

Troubleshooting capabilities

Education

Degree in Engineering, Biotechnology, Pharmaceutical Sciences, or related discipline

Tools

Bioreactors

Filtration and concentration systems

Job description

Cagents is seeking an experienced Senior C&Q Engineer for a large-scale biopharma project in Limerick, Ireland. The role focuses on the hands-on execution and optimisation of bioprocessing systems, including commissioning and qualification of equipment like bioreactors. Candidates should have over 10 years of experience in CQV and a strong knowledge of GMP standards.

This technically demanding position requires strong troubleshooting skills and the ability to work closely with cross-functional teams, ensuring that all systems meet Good Engineering Practice (GEP) standards.