Pharma Validation Engineer: Process/Equipment & GMP

Servier Group; Ireland; On-site; EUR 55,000 - 75,000; Full time

Job summary

Servier Group in Ireland seeks a Validation Engineer in the Quality division to coordinate, execute and report Process, Transport and Cleaning Validation activities, and to support equipment, facility and utility qualifications. You will prepare protocols, maintain validation documentation and support audits, root cause investigations and improvements to stay in a validated state.

The role requires 2–3 years of validation experience, a science or engineering degree, GMP exposure and strong

Qualifications

• Minimum 2–3 years validation experience.
• Third level degree in a Scientific or Engineering Discipline.
• Good knowledge of validation procedures and execution.
• Pharmaceutical experience.
• Experience in a GMP regulated environment.

Responsibilities

• Coordinate, execute and report Process, Transport and Cleaning Validation activities.
• Support equipment/system/facility/utility and laboratory qualification activities.
• Protocol preparation and Report writing.

Skills

Validation expertise

Process validation

GMP experience

Communication skills

Organisational skills

Education

Science/Engineering degree

Job description

Servier Group in Ireland seeks a Validation Engineer in the Quality division to coordinate, execute and report Process, Transport and Cleaning Validation activities, and to support equipment, facility and utility qualifications. You will prepare protocols, maintain validation documentation and support audits, root cause investigations and improvements to stay in a validated state.

The role requires 2–3 years of validation experience, a science or engineering degree, GMP exposure and strong