Summary:
The primary purpose of the Validation Supervisor role is to lead a QE Validation team and support any other QA activities on site as required.
Responsibilities:
1. Provide QE support for NPD/change control/feasibility etc. projects
2. Lead Validation Quality Engineering team
3. Mentor QEs through projects and ensure completion of projects per timelines
4. Plan resources and timelines for validation lifecycle activities to support NPD/change control projects etc.
5. Lead quality improvements in conjunction with Quality Manager
6. Complete Internal audits per the audit schedule
7. Support CAPA system
Essential Functions of the Role:
1. People Management
2. Problem Solving and Analyzing
3. Attention to detail
4. Change management
5. Goal Setting
6. Communicating/Leading
7. Processes Improvement
Work Experience Requirements:
* Number of Overall Years Necessary: 5-8
* Relevant experience in the medical device industry or equivalent regulated industry
* People Management experience desirable
Education Requirements:
* Degree in Engineering/Science Discipline and Quality Engineering Qualification or equivalent
* Certified Quality Engineer qualification or equivalent
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