Medical Device Manufacturing Engineer (Hybrid)

CREGG; Clonmel; Hybrid; Confidential; Full time

Job summary

CREGG is seeking a Manufacturing Engineer for our Clonmel site on a hybrid basis. The role focuses on introducing and validating new equipment, improving processes, and ensuring compliance with regulatory standards within a medical devices environment.

You will work with cross-functional teams to resolve issues, lead validation activities, and drive continuous improvement in equipment design, layout, and operational performance.

Qualifications

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

Responsibilities

• Introduce and validate new equipment.
• Analyze process specifications and performance requirements.
• Work with cross-functional teams to resolve production/engineering issues.
• Lead validation and qualification of equipment and processes.
• Drive continuous improvement and yield analyses.

Skills

Technical degree

Regulated environment

Medical devices

Education

NFQ Level 8

Tools

Automated equipment

Job description

CREGG is seeking a Manufacturing Engineer for our Clonmel site on a hybrid basis. The role focuses on introducing and validating new equipment, improving processes, and ensuring compliance with regulatory standards within a medical devices environment.

You will work with cross-functional teams to resolve issues, lead validation activities, and drive continuous improvement in equipment design, layout, and operational performance.