Validation Engineer

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

Validation Engineer Hybrid
About the role:

Our Clonmel based client are now recruiting for a Validation (Manufacturing) Engineer to join their team.

An excellent Hybrid working opportunity to work with a leading medical devices company.

This is a Projects role involving equipment introduction, line moves, equipment validation, equipment qualification, process improvements, line upgrades.

Responsibilities:

• Responsible for the introduction and validation of new equipment
• Analyses process, product, material or equipment specifications and performance requirements.
• Work with cross-functional teams to identify and resolve production/engineering issues.
• Summarises, analyses, and draws conclusions from test results leading to effective technical resolution.
• Transfer and validation of equipment from one clean room to another.
• Continuous Improvement & Yield Analysis.
• Continually seeks to drive / improvements in process equipment design, layout and operational performance.
• Engaging with technicians, operators, and other cross-functional teams to ensure business process success.
• Root cause analysis using Lean tools and techniques.
• Writing and improving process procedures.
• Demonstrates good working knowledge and application of validation techniques and associated regulatory requirements..

Qualifications and Experience:

• NFQ Level 8 in a Technical Discipline (Science, Biomedical, Mechanical, Manufacturing, etc.)
• Minimum 2-5 years’ experience working at an Engineering level, ideally in Medical Device industry or other highly regulated environment.