QC Technician II

Job Overview 

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. 

Job Responsibilities and Essential Duties

• 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. 

Minimum Requirements

• High school diploma or equivalent required; associate or bachelor’s degree in science, Math, Business, or a related field preferred. 
• 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 work 1st shift Monday - Friday 8AM - 4:30PM
• Ability to work overtime preferred, but not required

Required Knowledge, Skills and Abilities

• Ability to perform functional testing, inspections, and basic measurements accurately. 
• Prior Instron testing experience or prior training in one of the following Instron operator courses—Series IX, Merlin, or Blue Hill—is preferred. 
• 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.

Environmental/Safety/Physical Work Conditions

• Ensures environmental consciousness and safe practices are exhibited in decisions 
• Use of computer and telephone equipment and other related office accessories/devices to complete assignments 
• May work extended hours during peak business cycles 
• Ability to lift up to 40 pounds occasionally and handle materials, test fixtures, and equipment. 
• Must be able to perform repetitive motions, including frequent use of hands, wrists, and fingers for sample preparation, testing, and instrument operation. 
• Must be able to remain in a stationary or standing position for extended periods during testing. 
• Close visual acuity required for sample preparation, reading measurements, and data verification. 
• Must follow all safety and environmental requirements of the QC laboratory environment.
• This role requires working in a clean room manufacturing environment that involves wearing full gowning/Personal Protective Equipment (PPE).

Pay range:  $27 - $29 / hour and is eligilbe for our Excellence Incentive Plan (EIP), an annual incentive program that rewards performance against financial and operational goals. 

#LI-BS1