Associate Biomedical /MDR Vigilance Specialist

 Associate Biomedical / MDR Vigilance Specialist with 0-1 years experience.

Contract position for 12-24 months to work onsite in Mounds View, MN. 

As an Associate MDR/Vigilance Specialist, you will have the responsibility and authority to document and evaluate product feedback and product analysis results for products to determine complaint status and regulatory reporting status in conjunction with US and OUS regulatory guidelines.

Top 3 things the manager is looking for: 

1. Strong communication and writing/documentation skills

2. Biomedical, Biological, Medical Scribe other health care professional experience.

Top 3 Tasks or Responsibilities in scope for this role: 

1. Reviewing and documenting incoming medical device complaint info.

2. Making decisions on whether or not a report to the FDA is needed.

3. Reaching out to the field for further info on complaints

Top things looking for in a candidates experience:

1.  Strong attention to detail

2.  Strong analytical skills (problem solving critical thinking)

3.  Writing ability

4 Computer proficiency such as: (MS Office, SAP, etc)