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 today!
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
