Europe CQV Engineer: GMP Validation & Commissioning

Springtide; Dublin; On-site; EUR 70,000 - 100,000; Full time

Job summary

IPS is a global leader delivering commissioning, qualification and validation services for technically complex facilities in life sciences. The CQV Engineers/Consultants role involves on-site execution, documentation, and working across process, facilities and automation systems across Europe.

The position requires a degree in Engineering or Life Sciences, GMP project experience, IQ/OQ/PQ knowledge, and willingness to travel up to 100% to client sites.

Qualifications

• Degree in Engineering, Life Sciences or similar discipline
• Experience within Pharmaceutical, Biotech or Medical Device environments
• Experience with GMP-regulated projects
• Knowledge of IQ/OQ/PQ methodologies
• Experience with utilities, equipment, facilities, automation, or CSV preferred
• Ability to work on-site and travel across Europe when required

Responsibilities

• Develop and execute Commissioning, Qualification and Validation documentation
• Author IQ, OQ and PQ protocols and reports
• Support FATs, SATs and vendor testing activities
• Execute commissioning and qualification activities on-site
• Perform system walkdowns and punch-list management
• Review URS, FRS, DDS and technical specifications
• Support GMP compliance and regulatory requirements
• Investigate deviations and support CAPA activities
• Work across process, clean utility, facility and automation systems

Job description

IPS is a global leader delivering commissioning, qualification and validation services for technically complex facilities in life sciences. The CQV Engineers/Consultants role involves on-site execution, documentation, and working across process, facilities and automation systems across Europe.

The position requires a degree in Engineering or Life Sciences, GMP project experience, IQ/OQ/PQ knowledge, and willingness to travel up to 100% to client sites.