QC Technician II - Wayne, NJ

Getinge•Wayne, NJ

1d•$27 - $29•Onsite

About The Position

The Quality Control Technician II performs acceptance testing and inspection activities on in-process and finished goods to ensure products meet established requirements. This role is responsible for executing testing and inspection tasks accurately, documenting results in a timely manner, and supporting quality system compliance in a regulated manufacturing environment.

Requirements

High school diploma or equivalent required
Minimum of 2 years of experience in a quality function or regulated environment, or a bachelor’s degree or Certified Quality Technician (CQT) certification.
Experience in an FDA-regulated environment preferred; medical device experience strongly preferred.
Ability to perform functional testing, inspections, and basic measurements accurately.
Competence in reviewing documentation for completeness and compliance.
Ability to perform basic math across multiple units of measure.
Ability to use electronic quality systems and databases (e.g., SAP) for data entry and record maintenance.
Strong attention to detail and commitment to data integrity.
Effective verbal and written communication skills.
Ability to work collaboratively in a team environment.
Demonstrated flexibility and willingness to learn new tasks and procedures.
Ability to work independently, manage multiple priorities, and adapt to changing workflows.
Proficiency with Microsoft Office Products or equivalent software applications.

Nice To Haves

associate or bachelor’s degree in science, Math, Business, or a related field preferred.
Prior Instron testing experience or prior training in one of the following Instron operator courses—Series IX, Merlin, or Blue Hill—is preferred.

Responsibilities

Perform functional acceptance testing, and inspections on products assembled on the manufacturing floor in accordance with approved procedures and test methods
Conduct independent review of Shop Floor Paperwork (SFP) to verify completeness and accuracy prior to product release or further processing.
Identify and subject non-conforming materials to the NCMR process in accordance with established quality procedures.
Accurately document test results, inspections, and related quality records.
Read, comprehend, and follow job instructions, procedures, protocols, and work-related documents, including verbal and written directions.
Train Inspectors on acceptance testing methods, applicable procedures, and newly implemented policies, as assigned.
Assess daily priorities and adjust own work schedule as needed to support operational requirements.
Participate in team meetings and quality-related discussions as required.
Serve as the final quality control checkpoint for finished products, exercising accountability for release decisions to ensure patient safety.
Apply critical thinking, logical reasoning, and strong attention to detail when evaluating product acceptability and quality record completeness.
Collect, record, and maintain data required for Statistical Process Control (SPC) monitoring.
Perform routine SPC data trending to identify shifts, patterns, or early indicators of process instability.
Escalate emerging trends, anomalies, or risks to Quality Management to support proactive decision-making.
Develop an understanding of the full production workflow—from raw materials through final assembly—to improve judgment during final release.
Support the transition toward a proactive Quality Control environment by identifying opportunities to prevent defects rather than react to them.
Perform additional duties as assigned; responsibilities listed are not exhaustive.