Job Title: Validation Supervisor
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The primary objective of this role is to lead a Quality Engineering (QE) team and provide support for other QA activities on site as needed.
Key Responsibilities:
* Provide QE support for New Product Development (NPD), change control, and feasibility projects.
* Lead the Validation Quality Engineering team.
* Mentor Quality Engineers (QEs) through projects and ensure timely completion.
* Plan resources and timelines for validation lifecycle activities to support NPD, change control, and other projects.
* Lead quality improvements in conjunction with the Quality Manager.
* Conduct internal audits according to the audit schedule.
* Support the Corrective Action Preventative Action (CAPA) system.
Essential Functions:
* People Management
* Problem Solving and Analysis
* Attention to detail
* Change management
* Goal Setting
* Communication and Leadership
* Process Improvement
Work Experience Requirements:
* Minimum 5-8 years of overall experience
* Relevant experience in the medical device industry or equivalent regulated industry
* Desirable: People Management experience
Education Requirements:
* Degree in an Engineering or Science discipline
* Quality Engineering qualification or equivalent
* Certified Quality Engineer qualification or equivalent
This position requires a strong understanding of quality assurance principles, process improvement, and people management. The ideal candidate will have relevant experience in the medical device industry and be able to lead a team effectively.
Estimated Salary: $80,000 - $120,000 per annum, depending on experience