Find Jobs
Find Jobs Near You – Available Work in Your Location
Skip to job details
DR
DEKA Research & Development
Product Complaints Engineer
Career Insights for Product Quality Engineer
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on New Hampshire data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Product Quality Engineer evaluates and tests products and manufacturing systems, to ensure that products are produced that meet quality and performance standards as well as safety and regulatory requirements. Develops product quality standards and monitors production and product testing.
$100,820 / year median in New Hampshire
+4% projected growth
Job Description
Product Complaints Engineer DEKA Research & Development - 3.7 Manchester, NH Job Details Full-time 22 hours ago Qualifications Customer communication Bachelor's degree in engineering Full Job Description DEKA R D, on behalf of Millyard Advanced Medical Products, is looking for a Product Complaints Engineer to work in a dynamic Medical Device Research and Development environment. The position reports to the Product Complaints Manager. This is a high visibility role with a significant direct impact in the Quality Management System. How you will make an impact: Responsible for reviewing complaints related to potential medical device issues. Perform product complaint evaluations with minimal direction, utilizing experience and product knowledge. Ensure that complaint documentation follows Good Documentation Practices; meets QMS requirements; and complies with U.S. Food and Drug Administration (FDA) regulations / other regulatory requirements. Identify and make sound decisions regarding medical device reporting to regulatory agencies. Interface with Third Party Manufacturers, health care professionals, internal customers, and regulatory agencies. Participate in audits and CAPA investigations as they relate to complaint handling. Work with the forensic investigation team to align product investigations related to complaints. Generate reports to identify areas of process improvement. Develop product training aids. Contribute independently while also collaborating with other team members and departments needing product complaint information. Maintain positive and cooperative communication with co-workers, customers, contractors, and vendors. Serve as a subject matter expert on complaint handling. Perform other related duties as assigned under management supervision. Skills Needed to Be Successful Bachelor's degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Quality Engineering, or a related technical discipline required. Minimum of 3-5 years of experience in a regulated medical device, pharmaceutical, or life sciences environment, with direct responsibility for complaint investigations, product quality investigations, product analysis, and complaint closure activities. Demonstrated experience conducting complaint investigations, determining root cause, documenting investigation results, and independently driving records to closure in compliance with established timelines. Working knowledge of FDA Quality System Regulations, Medical Device Reporting requirements, and applicable standards, including 21 CFR Parts 803 and 820; experience with