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Viant Medical in Fort Wayne, IN is seeking a Quality Inspector to uphold ISO 13485 and FDA 21 CFR 820 standards, ensuring parts destined for life-saving devices meet exact print specifications.
You will read blueprints, perform inspections, document results, and maintain a tidy, compliant workspace while adhering to safety policies; shifts include 1st and 2nd with full-time hours.
At a glance
Company: Viant Medical
Location: Fort Wayne, IN (on-site)
Job Type: Full-Time
Pay Range: Competitive hourly pay (based on experience)
Shift: 1st Shift (2 openings); 2nd Shift also recruiting
Overtime: As needed
Experience Level: 2+ years inspection experience (medical device or regulated manufacturing)
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This role maintains elements of Viant Medical’s Quality Management System in accordance with ISO 13485 and FDA 21 CFR 820 requirements. Quality Inspectors are essential to confirming that parts destined for life-saving and life-enhancing medical devices meet exact print specifications before they leave the Fort Wayne facility.
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In this role, you will:
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Employees choose Viant Medical because of:
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Pay: Competitive hourly pay (based on experience)
Benefits (Day 1 Eligibility):
Schedule:
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Viant Medical is a global design and manufacturing services provider for the medtech industry, serving surgical technologies, orthopedics, cardiac and interventional, bioelectronics, bioprocessing, drug delivery, and diagnostics and lab markets. Viant partners with medical device makers from design and development through manufacturing, assembly, and packaging, and its Fort Wayne facility is FDA registered and ISO certified.