Analyst, Product Surveillance II in Minneapolis, MN at Volt

Date Posted: 11/6/2018

Job Snapshot

  • Employee Type:
  • Job Type:
  • Duration:
    44 weeks
  • Date Posted:
  • Job ID:
  • Contact Name
    Volt Branch
  • Phone

Job Description

Fieldglass: Job Posting

Contract-$33.00 depending on years of experience.  1 year contract, strong possibility of direct.

Volt Workforce Solutions has an outstanding opportunity for a well known industry leader in medical device.  This is for their Plymouth location.  Looking for entry to mid-level experience.

  •  Related experience in post market surveillance in a Medical Device or Pharmaceutical Industry. At least one year of experience with MDR and OUS regulatory reporting experience required. Knowledge of the use, development, and regulatory environment of medical devices.
  • Knowledge of 21 CFR Part 820, 198, Complaint Files, and 21 CFR Part 803, Medical Device Reporting.

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. Degreed applicants without medical, scientific, or complaint handling experience may be considered if they possess the strengths suitable for this position.

  • 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.
  • Medical Terminology or medical device reporting is a plus

Volt is an Equal Opportunity Employer