QC Technician II

Getinge; Wayne (AL); On-site; USD 37,000 - 43,000; Full time

Benefits offered by this job

Health, Dental, and Vision insurance

401k plan with company match

Paid Time Off

Wellness initiative & Health resources

Life Insurance

Short and Long Term Disability

Flexible Spending Accounts

Commuter Benefits

Parental and Caregiver Leave

Tuition Reimbursement

Job summary

Getinge in Wayne, NJ is seeking a Quality Control Technician II to manage the Nonconforming Material Report (NCMR) process and ensure compliance with quality systems. You will execute SAP transactions, support Incoming Inspection, and backup receiving inspection operations.

The role requires at least 3 years in a regulated quality function, experience with NCMRs, and strong documentation skills. This on-site position offers an incentive plan and a weekday schedule.

Qualifications

• Minimum 3 years of experience in quality functions within a regulated environment.
• FDA-regulated medical device experience ideal.
• Experience using SAP or other ERP systems.
• 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.

Responsibilities

• 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.

Skills

Organizational skills

Attention to detail

Communication skills

Data accuracy

Education

High School diploma or equivalent

Technical school experience

Tools

SAP

Job description

With a passion for life

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers.

Are you looking for an inspiring career? You just found it.

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.

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.