QC Technician II

Getinge

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.

Required Knowledge, Skills and Abilities

• 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.

This role is based in Wayne, NJ. The salary range for this position is $27.00 to $31.00 per hour

This role is eligible for participation in our Excellence Incentive Plan (EIP), an annual incentive program that rewards performance against financial and operational goals.

This shift reports at Monday - Friday 7:00 am to 3:30 pm EST

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About us

With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.

Benefits at Getinge:

At Getinge, we offer a comprehensive benefits package, which includes:

• Health, Dental, and Vision insurance benefits
• 401k plan with company match
• Paid Time Off
• Wellness initiative & Health Assistance Resources
• Life Insurance
• Short and Long Term Disability Benefits
• Health and Dependent Care Flexible Spending Accounts
• Commuter Benefits
• Parental and Caregiver Leave
• Tuition Reimbursement

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.

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© 2026 Getinge │ Getinge and GETINGE are trademarks or registered trademarks of Getinge AB, its subsidiaries or affiliates │All rights reserved. This information is aimed exclusively at healthcare professionals or other professional audiences and is for informational purposes only, is not exhaustive and therefore should not be relied upon as a replacement of the Instructions for Use, service manual or medical advice. Getinge shall bear no responsibility or liability for any action or omission of any party based upon this material, and reliance is solely at the user’s risk. Any therapy, solution or product mentioned might not be available or allowed in your country. Information may not be copied or used, in whole or in part, without written permission by Getinge. This information is intended for an international audience outside the US. Views, opinions, and assertions expressed are strictly those of the interviewed and do not necessarily reflect or represent the views of Getinge.