ZOLL Medical-posted 3 months ago
Intern
Pawtucket, RI
101-250 employees
Computer and Electronic Product Manufacturing

ZOLL Medical is a growing, innovation-driven company on the forefront of delivering medical devices to save lives, and software solutions to improve efficiency. With customers in more than 140 countries, we continue to expand our reach, as well as our product offerings. Hospitals, emergency medical services (EMS), and others trust us to provide high-quality products and exceptional customer service. ZOLL products are used every day across the globe to save the lives of people who suffer sudden cardiac arrest. From Real CPR Help technology-an industry first-to the world's only wearable defibrillator, our capabilities and features set us apart. But none of this would be possible without the motivation and dedication of ZOLL employees, and we're invested in their success. This position runs from January 2026 to August 2026 and requires candidates to be enrolled in a degree program at the start of the Co-op.

  • Assist Supplier Quality Engineers with reviews of supplier performance data, in evaluation and validation of supplier change requests, generates brokerage component MCOs and supplier validation summaries, along with driving improvements in supplier's delivered quality for both new product introductions and sustaining products.
  • Demonstrate ability to work with suppliers and other members of ZOLL's quality department in identifying possible root causes of recurring defects/issues and implementing systemic process improvements.
  • Provide daily quality support for issues arising in incoming inspection, MRB and on the production lines, using sound engineering judgement in the disposition of product through the material review board process.
  • Maintain the Supplier History database, Supplier Corrective Action Database, and Supplier audit schedule.
  • Perform other duties as required.
  • Desire and ability to comprehend and comply with standards and regulations such as ISO13485, ISO9001, and FDA 21 CFR Part 820.
  • Must be currently pursuing a Bachelor's degree or above in an Engineering discipline.
  • Must be a self-managed, hard-working, self-motivated individual.
  • Excellent verbal and written communication skills.
  • Proficient in most common PC based applications (Word, Excel, PowerPoint, Project, Visio, etc.)
  • Experience working in a fast-paced environment with diverse multidisciplinary teams.
  • Background in quality and engineering processes.
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