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ZM
Zoll Medical Corporation
Quality Assurance Compliance Engineer
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Based on Massachusetts data
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What they do
A Quality Assurance Auditor regularly evaluates the quality control systems in place and verifies compliance with quality and safety standards.
$70,678 / year median in Massachusetts
-4% projected decline
Job Description
Quality Assurance Compliance Engineer Zoll Medical Corporation - 3.4 Chelmsford, MA Job Details $90,000 - $110,000 a year 1 day ago Qualifications Bachelor's degree Full Job Description Acute Care Technology 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 Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Products include AEDs, trauma kits, ventilators, temperature management solutions, and more. 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. Due to the on‑site requirements of this position, applicants are expected to reside within a reasonable commuting distance of the designated work location (Chelmsford, MA). This role does not offer relocation. ZOLL Medical does not provide immigration-related sponsorship for this role. Do not apply for this role if you will need ZOLL immigration sponsorship (e.g. H1B, TN, STEM, OPT, etc.) either now or in the future. 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 Support managers and supervisors to define training requirements and ensure employees are trained to adequately perform their assigned responsibilities related to the Quality Management System. 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, MDSAP and