Quality Auditor

Trane Italia•Noblesville, IN

1d•Onsite

About The Position

As a world leader in creating comfortable, sustainable, and efficient climate solutions for buildings, homes and transportation, it's our responsibility to put the planet first. For us at Trane Technologies, and through our businesses including Trane® and Thermo King, sustainability is not just how we do business—it is our business. Do you dare to look at the world's challenges and see impactful possibilities? Do you want to contribute to making a better future? If the answer is yes, we invite you to consider joining us in boldly challenging what's possible for a sustainable world. Learn about our benefits designed for you to Thrive at work and at home. We boldly go. As a Quality Auditor, you will perform quality audits to validate operational performance of temperature-controlled storage units, refrigerators/freezers and thawing systems. Cross-trained to perform specialty functions.

Requirements

1-3 years manufacturing related experience
High school diploma or GED required.
Must be able to read and understand work instructions in English.

Nice To Haves

MRP/ERP preferred
Wiring skills/training preferred and electrical knowledge will be developed after hire.

Responsibilities

Promotes values as demonstrated in personal productivity and quality of work, management of internal/external relationships, actively seeking out and participating in Continuous Improvement practices, and willingness to engage and support team initiatives.
Comply with workplace safety procedures.
Regular and reliable attendance, which includes punctuality and working scheduled overtime, is necessary to meet our commitment to provide quality products and service to our customers.
Perform quality audits
Unit preparation
Unit start up procedures and validation
Unit shut down procedures and validation
Wiring and electrical performance of unit
Visual review acceptance of unit
Calibration of units
Performs quality audits and documentation of work performed
Follows work instruction to determine the process required.
Record measurements as needed.
Ensure that device history records are completed according to FDA GMP requirements.
Complete nonconformance records according to established procedures and GMP requirements.
Troubleshoot equipment failures.
Various assembly activities.
Train new employees by demonstrating work.