Package:
1. Full Time / Permanent
2. €70k – €75k+ Basic (Dependent on Experience & Open to Negotiation)
3. Annual Bonus (7.5%)
4. Health Insurance
5. Pension (4%/8%)
6. Paid Annual Leave
7. Parking
8. Educational Assistance
9. Relocation Budget (€)
Role:
The primary purpose of the Validation Supervisor is to lead the QE Validation Team and support any other QA activities on site as required.
Stakeholders: Engineering, Manufacturing, Supply Chain Management, Product Development and Corporate Quality Management and R&D.
Duties:
10. Lead Quality Engineering Team (7 Direct Reports)
11. Provide Quality Engineering support for New Product Development, Change Control and Feasibility Projects
12. Mentor QEs through projects and ensure completion of projects per timelines
13. Plan resources and timelines for validation lifecycle activities to support NPD / change control projects etc. in collaboration with engineering
14. Lead quality improvements in conjunction with Quality Manager
15. Complete Internal audits per the audit schedule
16. Support CAPA system
Experience:
17. Third Level Qualification in Science, Engineering, or related discipline
18. 5-8 Years Quality Engineering experience in Medical Device Industry utilizing Automated Equipment
19. Experience in Statistical Analysis / SPC / Validation of Automated Equipment