The core responsibility of the Quality Inspector Technician is to perform quality inspections while providing overall support to both Quality and cross-functional departments as necessary.

Additional responsibilities include conducting inspection of all incoming orthosis design components, mid-process checks, and a final outgoing inspection on devices prior to shipment. The QC tech will initiate NCMRs for nonconforming materials and devices, offering testing support to quality and engineering as well.

Responsibilities 

• Conduct inspection of incoming product components.
• Initiate NCMRs for nonconforming materials; conducting data collection and testing for NCMRs as appropriate.
• Ability to sort materials and components as needed.
• Assist with rework, device servicing, and repairs. (NCMRs)
• Perform in-process quality inspections and checks, as well as final inspection and device testing prior to outgoing shipments.
• Provide quality support to New Product Development, as well as execution of tasks and assignments for QC Manager on an ad hoc basis.

Qualifications 

• 3 Years’ Quality Inspection experience within the medical device industry.
• Experience writing nonconforming material reports
• High School or Trade school diploma required; some college preferred.
• FDA – GMP experience and training a plus.
• Technical training and/or certifications a plus.
• Electro-mechanical device background with assembly or inspection.
• Familiarity with components, materials testing, inspection tools, product rework, and equipment.
• Teamwork-oriented mindset with the ability to follow instructions and procedures; capability to independently complete forms and submit paperwork