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Junior Quality Engineer

DEKA Research and Development
United States, New Hampshire, Manchester
340 Commercial Street (Show on map)
Apr 04, 2025
DEKA Research & Development, located in Manchester, NH, isseeking a Junior Quality Engineer to provide design quality support in a dynamic, fast-paced environment of medical device R&D and manufacturing.

How you will make an impact as a Junior Quality Engineer:
  • Work cooperatively with other team members and in compliance with applicable standards and regulations such as 21 CFR 820 and ISO 13485:2016
    • Evaluate project and design compliance to applicable standards and regulations
  • Use critical thinking and analysis to determine the best approach and provide guidance on QMS compliance to design team members
  • Support development of complex electromechanical devices including software through quality system processes
  • Participate in Risk Management activities in accordance with ISO 14971:2019 such as FMEAs and Risk Analysis
  • Assist in the development, implementationand approval of Device Master Records and Device History Records
  • Participate in investigations resulting in root cause and corrective actions through use of data analysis, inductive and deductive reasoning, and problem solving skills
    • Coordinate the efforts of individuals and teams performing investigations
  • Ensure the accurate documentation and recording of information to be used in communication with partners and regulatory bodies
  • Support system and process improvements using six sigma tools
  • Support reliability and statistical analysis
  • Support in internal and external audits
To be successful in this role as a Junior Quality Engineer, you will need the following skills:
  • Bachelor's degree in Biomedical, Mechanical, Electrical, ora related engineering discipline
  • Ability to work as part of a multidisciplinary team
  • Excellent verbal and written communication skills, as well asattention to detail
  • Ability to understand and provide guidance on quality system procedures
  • 1+ years of experience in any suitable occupation related to quality control of medical devices preferred
  • Completion of Capstone, Co-Op, or Internship project in the medical device field preferred
  • Experience with medical devices and Risk Analysis and Design Transfer preferred
  • Experience with compliance to applicable standards and regulations such as 21 CFR 820 and ISO 13485:2016 preferred

About DEKA:

One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age.

Behind DEKA's brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.


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