Location: Saint Paul,MN, USA
Role: Product Surveillance Analyst
Location: St. Paul, MN - 55117/100% onsite position
Duration: 11 Months contract to hire
Shift Timings: 7 AM to 4 PM OR 9 AM to 6 PM
Position will be located either at Plymouth, MN, location at 5050 Nathan Lane N, or St. Paul, MN location
The ability to travel to both locations is a required.
Job Description:
Years Experience: 0 - 2 years
Skills: Related experience in post market surveillance in a Medical Device or Pharmaceutical Industry preferred.
Complaint handling, investigation of product performance experience nice to have
Someone with lab experience for investigation
Manage complaint file start to end good communication
Education: Four-year degree, preferably in the healthcare or science fields; or 2-year degree and relevant experience supporting complaint handling investigations, medical device reporting, or product analysis.
This position will analyze and submit complaints and/or investigate returned products from the field (some biohazard as they are used in surgery).
Degreed applicants without medical, scientific, or complaint handling experience may be considered if they possess the strengths suitable for this position.
Duties:
May perform multiple functions within the postmarket surveillance department.
Major responsibilities would include determining classification, review, and disposition of adverse events and medically related complaints for on-market products, including decisions on seriousness, reportability, and potential causality.
Complete FDA MDR and other outside competent authority regulatory reports