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 equivalent
• Proficiency in MS Office Suite
• Working knowledge of FDA regulations and standards such as ISO 13485 and FDA Quality System Requirements