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Viant is a global medical device design and manufacturing services provider that partners with customers to deliver high‑quality, life‑enhancing medical devices. This role focuses on maintaining elements of Quality Management Systems in line with ISO 13485 and FDA 21 CFR 820, and company protocols.
You will work on reliability and precision inspection, reading blueprints, and ensuring documentation accuracy while adhering to safety and quality standards.
Posted Wednesday, July 29, 2026 at 4:00 AM
We partner and innovate with our customers to provide the highest quality, life enhancing medical devices in the world.
1 st Shift (M-F 7am-3pm)
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.