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Viant Medical in Fort Wayne, IN, is hiring a Quality Inspector to maintain QMS elements in line with ISO 13485 and FDA 21 CFR 820. You will inspect parts, read drawings, and document results, ensuring compliance and timely throughput.
The role requires 2+ years of medical device inspection experience, GD&T knowledge, and the ability to interpret prints. On-site responsibilities include safety adherence and teamwork in a climate-controlled environment.
We partner and innovate with our customers to provide the highest quality, life enhancing medical devices in the world.
2nd shift
This position will work to maintain elements of Quality Management Systems (QMS) in accordance with ISO 13485 and FDA 21 CFR 820 requirements as well as company protocols.
Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. We do this through our depth and breadth of capabilities, end-to-end integration, technical expertise, and relentless focus on our customers and on operational excellence. With nearly 6,000 associates across 24 locations worldwide, we offer a unique combination of small-company service and attention with big-company resources. For more information, visit viantmedical.com or follow us on LinkedIn.
Viant provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Viant complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities.