C&Q Engineer - GMP Pharma Commissioning & Validation

Adecco Portugal; Waterford; On-site; EUR 45,000 - 75,000; Full time

Job summary

A Commissioning & Qualification (C&Q) Engineer is sought to lead qualification activities for pharmaceutical facilities, focusing on GMP regulated lifecycle activities and utilities. This role involves hands-on testing, commissioning of laboratory systems, and collaboration with cross-functional teams to meet project milestones.

The position is on-site in Ireland for a 12-month contract, with standard business hours and flexibility to support critical project milestones in a fast-paced regulated

Qualifications

• Degree or equivalent qualification in Engineering, Life Sciences, or a related technical discipline.
• Experience in a C&Q, Validation, or Engineering role within the pharmaceutical, biotechnology, or regulated manufacturing industry.
• Strong knowledge of GMP and qualification lifecycle activities
• Experience with manufacturing equipment, utilities, facilities, or laboratory systems qualification.

Skills

GMP knowledge

Qualification lifecycle

CAPEX projects

Laboratory systems qualification

Cross-functional collaboration

Education

Engineering/Life Sciences degree

Job description

A Commissioning & Qualification (C&Q) Engineer is sought to lead qualification activities for pharmaceutical facilities, focusing on GMP regulated lifecycle activities and utilities. This role involves hands-on testing, commissioning of laboratory systems, and collaboration with cross-functional teams to meet project milestones.

The position is on-site in Ireland for a 12-month contract, with standard business hours and flexibility to support critical project milestones in a fast-paced regulated