Quality Control Inspector II

Company Overview:

AVS is an early-stage medical device company focused on safely and effectively treating severely calcified arterial disease. It was founded in 2018 by Hitinder Gurm, M.D., Interventional Cardiologist and Chief Clinical Officer at University of Michigan, and Robert Chisena, Ph.D., Chief Technical Officer at AVS. We are redefining interventional therapy for severely calcified lesions with our Pulse IVL System, which uses a novel pulsatile mechanism of action to shatter calcium and expand narrowed vessels, all with a single device. To learn more about pulsatile intravascular lithotripsy, visit

In May of 2026, Stryker acquired Amplitude Vascular Systems, a medical device company focused on safely and effectively treating severely calcified arterial disease.

Stryker is a global leader in medical technologies and, together with our customers, we are driven to make healthcare better.

We offer innovative products and services in MedSurg, Neurotechnology and Orthopedics that help improve patient and healthcare outcomes. Alongside our customers around the world, we impact more than 150 million patients annually.

More information is available at

Position Summary:

Under general supervision, assembles components that may include sub-assemblies, manual components and electrical components and all other related components to contribute to completion of a variety of products. Adheres to safety, quality and quantity standards and follows directions and blueprints to meet product specifications.

About the Role

The QC Inspector II perform inspections of the manufacturing process. Conducts dimensional and electrical inspection of sub-assemblies or final systems assemblies. Interprets prints, manufacturing drawings, diagrams, wire cards and lists in approving or rejecting in-process or final assemblies.

Under general supervision, follows written and/or verbal instructions to perform moderately complex Quality Control tasks.

Key Responsibilities

• Inspects raw materials, components and finished products to ensure conformance to specification.
• Perform inspection of the production lines and document all findings.
• Performs quality control inspections in accordance with FDA, ISO, and other applicable regulations / guidelines.
• Accurately records inspection results to ensure proper segregation of accepted and rejected products.
• Will follow team practices and company policies to:
• Conduct Incoming/ In-process Quality Control activities associated with components, assemblies, and/ or electro-mechanical products
• OR
• Conduct Final Quality Control Release activities associated with completed customer orders/ products
• Will ensure acceptance activities, including documentation requirements (depending on the situation, this may include review of packaging, labeling, product literature, and/ or revision levels) are met for accepted products.
• Will comply with all quality, regulatory, and documentation procedures and policies.
• Will follow Line Clearance Policy, maintaining inspection gear and overall workstation cleanliness and organization.
• Will provide customer service support to internal customers (Quality, Operations, Materials, Engineering, or Divisional teams)
• Will interact with internal customers to resolve quality control issues.
• Will execute projects independently.
• May train and mentor QC Inspectors I’s.
• May provide inspection technique, process, or procedure training to others.
• May interact with suppliers and other external customers to resolve quality control issues.
• May work from engineering schematics or blueprints to perform accurate checks and tests.
• May work with calibrated gauges, tools, and equipment.
• May represent team during Internal/ External audits.
• May help devise and utilize non-standard inspection procedures.
• May participate in or lead QA improvement projects.
• May be required to operate a CMM (Coordinate Measuring Machines) or similar equipment.

Required Qualifications

• High school diploma or its equivalent .
• Preferred Education/Training-GD&T training, ASQ Certified Quality Inspector (CQI) or equivalent certification/ experience, Formal technical/ Quality control training or equivalent experience
• 2+ years of experience in quality inspection in the medical device industry, preferred
• Ability to meet work schedule and meet overtime requirements, including weekends
• Ability to read and understand procedures, safety sheets, instructions and policies in English
• Ability to carry out verbal instructions and communicate verbally in English
• Excellent problem-solving and analytical skills
• Attention to detail
• Some problem-solving skills are required.
• Documentation and reporting skills
• Teamwork and collaboration
• Basic computer and math skills to calibrate and measure specifications
• Ability to use measuring devices like gauges, meters, calipers and computers.
• In-depth understanding of company standards.
• Up-to-date knowledge of federal and industry standards and best practices.