Senior Validation Engineer - GMP & CQV Lead (Dublin)

Cagents; Dublin; On-site; EUR 65,000 - 85,000; Full time

Job summary

Cagents is looking for a Senior Validation Engineer in Dublin, Ireland, to lead commissioning and validation activities for packaging and assembly lines. This role requires expertise in GMP compliance and 5-10 years of validation experience in the Pharmaceutical/Life Sciences industry.

As a Senior Validation Engineer, you will support project teams by developing and executing validation protocols, ensuring all documentation is compliant, and collaborating with cross-functional teams to achieve timely delivery and compliance.

Qualifications

• Bachelor’s degree in Engineering preferred; relevant experience may substitute for education.
• Minimum 5-10 years of experience in validation roles within the Pharmaceutical/Life Sciences industry.
• Strong knowledge of packaging equipment, inspection systems, and serialization/aggregation solutions.

Responsibilities

• Lead end-to-end validation activities in a GMP environment.
• Create and review validation documentation including Validation Master Plans.
• Support scoping, planning, and execution of validation projects.

Skills

GMP regulations

Validation documentation

Problem-solving

Communication

Risk-based validation

Education

Bachelor's degree in Engineering

Tools

Packaging equipment

Serialization systems

Job description

Cagents is looking for a Senior Validation Engineer in Dublin, Ireland, to lead commissioning and validation activities for packaging and assembly lines. This role requires expertise in GMP compliance and 5-10 years of validation experience in the Pharmaceutical/Life Sciences industry.

As a Senior Validation Engineer, you will support project teams by developing and executing validation protocols, ensuring all documentation is compliant, and collaborating with cross-functional teams to achieve timely delivery and compliance.