What are the responsibilities and job description for the Biomedical Engineer position at Bentley Global Resources and Staffing Services?
**US Citizen or Green Card/Permanent Resident ONLY**
**WE DO NOT work with 3rd parties**
Education Required: Bachelors Degree
Years’ Experience Required: 0-2 years
Schedule:
- Onsite Monday and Tuesday
- Remote Wednesday, Thursday, and Friday
In this exciting role 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.
In conjunction with US and OUS regulatory reporting criteria, the Associate MDR/Vigilance Specialist compiles regulatory agency reports for submission.
As part of complaint closure activities this individual performs activities to monitor complaint activity to ensure timely review of product feedback, product analysis, product formal investigation, and any associated follow-up actions that pertain to complaint closure.
Responsibilities include the following but not limited to:
- Apply policies and procedures to comply with FDA and OUS regulations.
- Monitors the company's drug or medical devices surveillance program including the intake, protocol development, evaluation, processing, and follow-up on adverse event reports, complying with government regulations.
- Evaluate incoming information to determine Medical Device Reporting and Vigilance reporting eligibility.
- Ensures complete, accurate, and timely submission of Medical Device Reports (MDRs), Vigilance Reports (VR) Adverse Drug Experience (ADE) data or adverse reaction data as required by regulatory agencies.
- Interface and collaborate with internal and external contacts to ensure appropriate collection of complaint information in an efficient and customer focused manner.
- Maintain awareness of new products, government regulations and requirements.
- Acts as a liaison internally and with external collaborators to develop programs and processes to meet regulatory reporting requirements
- Other duties as assigned.
Salary : $22 - $27