Summary

The Quality Control Technician II is responsible for the administration and execution of the Nonconforming Material Report (NCMR) process. This position manages the lifecycle of nonconforming material from NCMR creation through final disposition, ensuring compliance with quality system requirements and inventory controls. The role performs SAP transactions to place material on quality hold, maintain inventory segregation, and release material following approved disposition. The position also provides support to Incoming Inspection activities and serves as a backup resource for receiving inspection operations.

Job description

Job Overview

The Quality Control Technician II is responsible for the administration and execution of the Nonconforming Material Report (NCMR) process. This position manages the lifecycle of nonconforming material from NCMR creation through final disposition, ensuring compliance with quality system requirements and inventory controls. The role performs SAP transactions to place material on quality hold, maintain inventory segregation, and release material following approved disposition. The position also provides support to Incoming Inspection activities and serves as a backup resource for receiving inspection operations.

Job Responsibilities and Essential Duties

Create, initiate, and maintain Nonconforming Material Reports (NCMRs) in accordance with Quality System procedures.
Review nonconforming material documentation for accuracy, completeness, and compliance.
Coordinate NCMR activities between Manufacturing, Quality Engineering, Supplier Quality, Materials, and Operations.
Facilitate timely review and disposition of nonconforming material by the appropriate stakeholders.
Maintain NCMR metrics and provide status updates to management.
Ensure proper documentation of dispositions including: Use-As-Is, Rework, Return to Vendor (RTV), Scrap.
Verify all required approvals and supporting documentation are completed prior to NCMR closure.
Participate in Material Review Board (MRB) meetings as required.
Support investigations related to nonconforming material.
Maintain accurate inventory status for restricted, quarantined, and dispositioned materials.
Coordinate SAP material movements associated with NCMR dispositions.
Investigate and resolve inventory discrepancies related to quality holds and released material.

Minimum Requirements

A High School diploma, or equivalent, is required; 2 years technical school or equivalent experience preferred.
Minimum 3 years of experience in quality functions within a regulated environment; FDA-regulated medical device experience ideal.
Strong organizational and follow-up skills.
Strong written and verbal communication skills, attention to detail and data accuracy.
Experience using SAP or other ERP systems required.
Ability to interpret procedures, specifications, and manufacturing documentation.
Minimum 2 years of experience in a quality, manufacturing, or regulated industry environment.
Experience with NCMRs, nonconforming material control, or quality systems preferred.
Medical device, pharmaceutical, or other regulated industry experience preferred.

Requirements

High School diploma or equivalent required
Minimum 3 years of experience in quality functions within a regulated environment
Experience using SAP or other ERP systems required
Minimum 2 years of experience in a quality, manufacturing, or regulated industry environment
Strong organizational and follow-up skills
Strong written and verbal communication skills
Attention to detail and data accuracy
Ability to interpret procedures, specifications, and manufacturing documentation

Benefits

Health, Dental & Vision Insurance
401(k) Matching
Paid Time Off
Wellness Initiative
Health Assistance Resources
Life Insurance
Short & Long Term Disability
Flexible Spending Accounts
Commuter Benefits
Parental & Caregiver Leave
Tuition Reimbursement
Excellence Incentive Plan

Company overview

Getinge AB is a leading Swedish medical technology company founded in 1904 and headquartered in Gothenburg, Sweden. As a publicly traded company listed on Nasdaq Stockholm, Getinge specializes in developing and manufacturing advanced medical devices and solutions for healthcare and life sciences industries. The company operates through three core business areas: Life Science, Acute Care Therapies, and Surgical Workflows. Getinge's comprehensive product portfolio includes ventilators, heart-lung machines, anesthesia systems, surgical tables, sterilizers, washer-disinfectors, bioreactors, and digital health solutions. With approximately 12,000 employees worldwide, operations in 40 countries, and sales in over 135 countries, Getinge has established itself as a global leader in medical technology. The company maintains manufacturing facilities across Europe, Asia, and North America, with the United States representing its largest market. Getinge's commitment to innovation and patient safety has made it a trusted partner for hospitals, research laboratories, and pharmaceutical production facilities worldwide, dedicated to improving clinical outcomes and optimizing healthcare workflows.