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.

Customer

We focus on our customers’ success

Innovation

We create better solutions

Collaboration

We create success together

Inclusion

We always interact with others respectfully

Candor

We are open and honest with one another

Integrity

We do the right things and do things right

Key Accountabilities and Responsibilities

1. 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.

2. 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.

3. Review all product non-conformances and determine necessary corrective actions.

4. Monitor/track QA/QC department metrics and develop continuous improvement plans that drive site Gs&Os.

5. Oversee incoming/in-process sub-components and finished goods. 

6. Support Quality Engineering and Manufacturing Engineering in the resolution of non-conforming materials.

7. Supervises Associates in a manner that fosters a safe work environment and self-directed team approach.

8. Promotes an atmosphere of diversity, open communication and trust, affording opportunities for training and growth.

9. Identifies, arranges and/or provides training to ensure a safe, efficient, quality work environment with focus on continuous improvement through Lean manufacturing principles.

10. Facilitates communication, coordination and conflict resolution within and among work groups.

11. Provides leadership to Associates in all areas including:  hiring, performance management, coaching, counseling, and corrective actions.

12. Performs other functions as required.

Job 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.

Salary for this position is $91,575 - $134,310 per year

U.S. Applicants: EOE/AA Disability/Veteran