QA Compliance Engineer

Location: Deerfield, WI, United States of America


At ZOLL, we're passionate about improving patient outcomes and helping save lives.

We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions.

The Resuscitation division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service.

At ZOLL, you won’t just have a job. You’ll have a career—and a purpose.

Join our team. It’s a great time to be a part of ZOLL!

Job Summary

This individual will drive Quality Improvements through the Corrective and Preventative Action program in a cross functional environment. Support the Organizations Internal Audit program and participate in external audits to ensure we maintain regulatory compliance. Assist with content review for Quality System documents and regulatory communication.

Essential Functions
  • Review CAPA(s) for appropriate content Monitor and Manage CAPA KPl(s) to objectives
  • Ability to lead a cross-functional team through CAPA
  • Maintain and look for opportunities to continuously improve the CAPA process and compliance to all applicable regulations
  • Conduct appraisals program yearly or as needed for CAPA Leads Assist in the development, training and expectation for CAPA Leads Assist in the management and scheduling for Internal Auditing Ensure internal audit finding response time meets internal targets Ensure timely closure of internal audit responses
  • Participate in external audits related to manufacturing site under QMS umbrella Ensure timely QS compliance related to SOP review
  • Assist in the review of Health Risk Assessment's
  • Assist in the development and review of Competent Authority, Registrar and Regulatory Agency correspondence

Required/Preferred Education and Experience
  • Four-year degree required
  • Minimum 5 years related experience in a regulated environment, preferably Medical Device Industry preferred

Knowledge, Skills and Abilities
  • Excellent written, verbal and interpersonal communication skills Proficient time management and project management skills
  • Experience with FDA QSR, ISO13485, MDD and MDR, ISO14971 for Medical Devices
  • Proficient with auditing techniques

ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients' lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives.