Are you an experienced validation engineer looking for a new opportunity in Cork, Ireland?
Do you have experience with automation equipment in a manufacturing environment and within the life sciences industry?
Are you interested in joining a global leader in medical technologies?
Don't hesitate apply todayp>
Job Description
Our client are seeking an experienced validation engineer who can provide advanced technical and engineering support for upcoming projects in their manufacturing division.
This engineer will use the required engineering competencies to support their team.
Responsibilities
Responsible for managing and delivering key project tasks assigned
Work with automation vendors, engineering, and other functions in delivering key project task assigned
Generate, review, and approve project validation documentation URS, PFMEA's FAT, SAT, VP, IQ, OQ, PQ, reports, procedures, and other documents as required compliant with current Good Manufacturing Practices (GMP)
Execute validation qualification test protocols documents
Support debugging the automated system with structured problem solving and providing feedback to the project team and vendor
Support install of the automation system at the site in readiness for qualification.
Requirements
Level 8 Degree in Mechanical Engineering
Proven validation experience
2-4 years' experience in a manufacturing environment
Experience in an FDA regulated or regulated industry beneficial
Benefits
Competitive and attractive employee compensation package
Pension contributions
Health insurance
Paid public holidays
Location
Cork, Ireland
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