Hybrid Validation Engineer - Medical Devices

CREGG Group; Tipperary; Hybrid; EUR 48,000 - 75,000; Full time

Job summary

CREGG Group in Ireland is seeking a Validation (Manufacturing) Engineer to join a Clonmel-based team on a hybrid basis. The role focuses on equipment introduction, validation, qualification, and process improvements within a highly regulated medical device environment.

Responsibilities include validating new equipment, analyzing specifications, collaborating with cross-functional teams, transferring equipment between clean rooms, and applying Lean tools for continuous improvements.

Qualifications

• NFQ Level 8 in a technical discipline.
• 2–5 years’ engineering experience in regulated environments.
• Experience in validation techniques and regulatory requirements.
• Background in medical devices preferred.

Responsibilities

• Lead introduction and validation of new equipment.
• Analyze specifications and performance requirements.
• Collaborate with cross-functional teams to resolve issues.
• Transfer and validate equipment between clean rooms.
• Apply Lean tools for root cause analysis and improvements.

Skills

Validation

Manufacturing

Equipment validation

Lean tools

Education

NFQ Level 8

Job description

CREGG Group in Ireland is seeking a Validation (Manufacturing) Engineer to join a Clonmel-based team on a hybrid basis. The role focuses on equipment introduction, validation, qualification, and process improvements within a highly regulated medical device environment.

Responsibilities include validating new equipment, analyzing specifications, collaborating with cross-functional teams, transferring equipment between clean rooms, and applying Lean tools for continuous improvements.