Validation Supervisor

at  Hollister incorporated

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

RESPONSIBILITIES:

• Provide QE support for NPD/change control/feasibility etc. projects
• Lead Validation Quality Engineering team – Ostomy
• Mentor Ostomy 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 Ostomy engineering
• Support Ostomy Compliance activities as assigned and 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