Post Market Surveillance Specialist in Andover, MA at Eliassen Group

Date Posted: 12/9/2019

Job Snapshot

  • Employee Type:
  • Location:
    Andover, MA
  • Job Type:
  • Experience:
    Not Specified
  • Date Posted:

Job Description

We have an excellent opportunity available for a Post Market Surveillance Specialist with one of the most respected companies in the Life Sciences industry. Our client is a multi-billion dollar leader in the manufacturing of innovative products in the Medical Device space. If you are passionate about making an impact with a company, who’s goal it is to improve the quality of life for millions of people, we’d like to talk with you! 

This is a contract position that is expected to go, at least, for 6 months.

In this role you will be responsible for: 

  • Handling the receipt, processing, monitoring, and reporting of product defect complaints
  • Making MDR determination
  • Investigating and documenting all activities and creating the summaries of the investigation
  • Ensuring the process is completed in accordance with standard procedures.
  • Following complaint files through completion.
  • Determining complaint codes (Product & Incident). 

The client would like to see:

  • Experience in post-market complaints in an FDA regulated industry.
  • Bachelor’s degree in engineering, clinical sciences or
  • Proficiency in MS Office Suite
  • Working knowledge of FDA regulations and standards such as ISO 13485 and FDA Quality System Requirements.