Supervisor, Quality

$91,575 - $134,310/Yr

Integer - Plymouth, MN

posted 2 days ago

Full-time
Plymouth, MN
Computer and Electronic Product Manufacturing

About the position

By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success. At Integer, our values are embedded in everything we do.

Responsibilities

  • Adheres to Integer values and all safety and quality requirements including, but not limited to: Quality Management Systems (QMS), Environmental Management Systems (EMS), U.S. Food and Drug Administration (FDA) regulations, Company policies and operating procedures, and other regulatory requirements.
  • Manage daily performance and attendance of Quality Assurance Technicians in the inspection and final release of sub-component parts and finished goods. Provide work direction and guidance throughout the shift on issues relating to Quality and schedule attainment.
  • Review all product non-conformances and determine necessary corrective actions.
  • Monitor/track QA/QC department metrics and develop continuous improvement plans that drive site Gs&Os.
  • Oversee incoming/in-process sub-components and finished goods.
  • Support Quality Engineering and Manufacturing Engineering in the resolution of non-conforming materials.
  • Supervises Associates in a manner that fosters a safe work environment and self-directed team approach.
  • Promotes an atmosphere of diversity, open communication and trust, affording opportunities for training and growth.
  • Identifies, arranges and/or provides training to ensure a safe, efficient, quality work environment with focus on continuous improvement through Lean manufacturing principles.
  • Facilitates communication, coordination and conflict resolution within and among work groups.
  • Provides leadership to Associates in all areas including: hiring, performance management, coaching, counseling, and corrective actions.
  • Performs other functions as required.

Requirements

  • Minimum Education: Bachelors in a related field.
  • Minimum Experience: At least 3-5 years of prior QA/QC Supervisory experience in a manufacturing environment preferred; medical device experience preferred.
  • Specialized Knowledge: ISO 1345, FDA 21 CFR Part 820 and other FDA requirements. Good Manufacturing Practices, Good Documentation Practices. Auditing training and experience preferred.
  • Special Skills: Geometric dimensioning and tolerancing (GD&T), gauging, and inspection methods.
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service