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Post Market Surveillance Specialist in Andover, MA at Eliassen Group

Date Posted: 3/13/2019

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.