Job Description:

• Responsible for managing the quality and compliance for applicable products and processes
• Adapt departmental plans and priorities to address resource and operational challenges
• Ensure quality and regulatory compliance with applicable regulations
• Acts as a liaison with the Divisions, Suppliers, Manufacturing, and Operations
• Manage complaints and develop new approaches to solve problems
• Identify and manage the execution of continuous improvement projects
• Assist the division in product evaluation from a quality assurance standpoint
• Ensure all quality issues are resolved to customer satisfaction

Requirements:

• Bachelor’s degree in Engineering, Science, or Technical Field
• At least 4 years of experience related to the design/operation of medical device or drug combination product platforms
• Must have experience with QSR/GMP/ISO requirements or other regulated industries
• Proficiency in analyzing and reporting data
• Advanced level skill in Microsoft Excel

Benefits:

• health insurance
• life and disability
• 401(k) contributions
• paid time off
• access to Employee Assistance Program
• access to Employee Resource Groups
• access to Employee Service Corp