Associate MDR/Vigilance Specialist

Three Point Solutions, Inc.
  • Mounds View, MN
  • $25–$30 Per Hour
  • Contractor
  • Instant Apply
16 days ago

Job Description

Job Title:          Associate MDR/Vigilance Specialist

Client:              Medical Device Manufacturing Company
Location:         Mounds View, MN 55112

 

Duration:         2 Years + Possible Extension
Shift:                1st Shift | Onsite

 

Description:

Job Summary

Support Medical Device Reporting (MDR), complaint handling, adverse event reporting, and medical device surveillance activities while ensuring regulatory and quality compliance.

Job Responsibilities

Key Responsibilities

·         Process and review MDR complaint records.

·         Support complaint handling and medical device surveillance.

·         Manage adverse event report intake, evaluation, processing, and follow-up.

·         Maintain accurate MDR and ADE records.

·         Review clinical databases and analyze safety data.

·         Prepare safety summaries and regulatory reports.

·         Ensure compliance with regulatory requirements and quality procedures.

·         Support regulatory reporting programs and processes.

·         Collaborate with internal teams and stakeholders.

·         Complete assigned projects and maintain accurate documentation.

Numbers & Facts

LocationMounds View, MN
Job TypeContractor
Salary$25–$30 Per Hour

Qualifications

Required Skills

·         Medical Device Reporting (MDR)

·         Complaint Handling

·         Regulatory Compliance

·         Medical Device Surveillance

·         Adverse Event / ADE Reporting

·         Clinical Database Review

·         Safety Data Management

·         Data Analysis & Documentation

·         Strong Critical Thinking

·         Excellent Organization & Time Management

·         Cross-functional Collaboration

 

Top Hiring Needs

·         Previous MDR experience

·         Excellent organizational and time-management skills

·         Strong critical-thinking skills

 

Qualifications

·         Bachelor's Degree required

·         1–3 years of relevant experience

·         Medical device or regulated-industry experience preferred

·         Clinical background (RN/healthcare professional) preferred

·         Biomedical Engineering background is a strong plus

·         Understanding of quality systems and regulatory requirements

 

Role Level

·         Entry-level individual contributor

·         Works under close supervision

·         Handles routine/less-complex projects

·         Supports process improvements and regulatory activities

About Company

Medical Device Manufacturing Company

Skills

  • Medical Device Reporting

Skills

  • Adverse Eventsunmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Medical Equipmentunmatched
  • Medical Office Administrationunmatched
  • Surveillanceunmatched

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