QA Compliance Engineer

Location: Deerfield, WI


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.

We offer competitive salaries and a comprehensive benefits package. 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

Skill Requirements:

  • 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

Required/ Preferred Education and Experience:

  • Four year degree

  • Minimum 5 years related experience in a regulated environment, preferably Medical Device Industry

Other Duties:

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job.  Duties, responsibilities, and activities will be reviewed periodically as duties and responsibilities change with business necessity.  Essential and marginal job functions are subject to modification.


ZOLL Medical Corporation appreciates and values diversity.  We are an Equal Opportunity Employer M/F/D/V. 


ADA:  The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990