Job Description
My client has a requirement for a Validation Team Leader for their facility in County Mayo.
You will need to have 5-8 Years Quality Engineering experience in the Medical Device Industry utilizing Automated Equipment.
Your responsibilities will involve leading the Quality Team (7) and supporting New Product Introductions.
A Full Time / Permanent role, we are offering a Relocation Budget for successful candidates who require moving to County Mayo – APPLY TODAY
Job Title: Validation Team Leader
Direct Reports: (7)
Location: County Mayo
Package:
- Full Time / Permanent
- €70k – €75k+ Basic (Dependent on Experience & Open to Negotiation)
- Annual Bonus (7.5%)
- Health Insurance
- Pension (4%/8%)
- Paid Annual Leave
- Parking
- Educational Assistance
- 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:
- Lead Quality Engineering Team (7 Direct Reports)
- Provide Quality Engineering support for New Product Development, Change Control and Feasibility Projects
- Mentor QEs through projects and ensure completion of projects per timelines
- Plan resources and timelines for validation lifecycle activities to support NPD / change control projects etc. in collaboration with engineering
- Lead quality improvements in conjunction with Quality Manager
- Complete Internal audits per the audit schedule
- Support CAPA system
Experience:
- Third Level Qualification in Science, Engineering, or related discipline
- 5-8 Years Quality Engineering experience in Medical Device Industry utilizing Automated Equipment
- Experience in Statistical Analysis / SPC / Validation of Automated Equipment