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:
* Provide QE support for NPD/change control/feasibility etc. projects
* Lead Validation Quality Engineering team
* 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.
* Lead quality improvements in conjunction with Quality Manager
* Complete Internal audits per the audit schedule
* Support CAPA system Essential Functions of the Role:
* People Management
* Problem Solving and Analyzing
* Attention to detail
* Change management
* Goal Setting
* Communicating/Leading
* 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 At Wallace Myers International Recruitment Agency we specialise in sourcing professionals for key industries and services. See our website for more details.
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For more info see Skills:
Quality Assurance Quality Professional Validation Medical Devices