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Sr. DQA Engineer

Sr. DQA Engineer

Job ID 
2017-1022
Job Locations 
US-MA-Chelmsford
Category 
Research & Development
Type 
Full-Time/Regular

More information about this job

Overview

ZOLL Medical Corporation is committed to developing technologies that help advance the practice of resuscitation. With products for pacing, defibrillation, circulation, ventilation, and fluid resuscitation, ZOLL provides a comprehensive set of technologies that can help clinicians, EMS professionals, and lay rescuers resuscitate sudden cardiac arrest or trauma victims. ZOLL also designs and markets software that automates the documentation and management of both clinical and non-clinical data.

We are looking for strong candidates who take initiative to continuously improve what they do in an effort to meet our customers' needs. We offer the challenge of working in a fast-paced team environment where your energy and expertise can help you to reach your full potential.

Responsibilities

Duties: Provide validation test development, execution, and results tracking for assigned projects in ZOLL Research & Development. Will conduct functional testing on all ZOLL deliverables, from standalone code to complete products and systems. Will be an active participant in product and subsystem requirements development, as well as Test Plan reviews.  Essential functions include:

 

  • Lead project validation test efforts
  • Implementing, reviewing and creating validation/verification test cases and test plans, both for DQA and the development teams.
  • Perform all testing as assigned
  • Identifying, reporting, and following up on test failures and observed defects
  • Work with the product development teams to isolate failure modes and capture methods to reproduce product problems
  • Reviewing and creating new/enhanced product requirements to ensure that the products are testable and meet both written and implied requirements

Qualifications

Requirements: Requires a Bachelor’s degree (or equivalent) in Biomedical Engineering, Software Engineering, Electrical Engineering, or a directly related field. 5+ years of experience in the Medical Device industry testing new products in a product development or research organization. Experience must include:

 

  • Knowledge and understanding of the underlying biomedical principals and how the products are used under clinical conditions strongly preferred
  • Clear understanding of effective software test design especially as it relates to system level testing of embedded systems
  • Working knowledge of Medical Device industry standards
  • Demonstrated accomplishments in the development of software and hardware testing processes and programs
  • Proficient with MS/Office, demonstrated ability to learn and use software engineering tools and applications in MS Windows and Linux environments
  • Excellent written, verbal and interpersonal skills

 

 

EOE/Minorities/Women/Vets/Disabled