Merit Medical Systems
Post Market Surveillance Specialist (Fixed-Term)
Utah - Virtual, USA
Sponsorship not specifiedDetected 5 days ago
Project ManagementFDA RegulatoryPharmacovigilanceMedical DevicesResearchCommunicationTime ManagementRegulatory Affairs
About the role
- Work Shift: DAY Work Schedule: Why Merit?
- This position is a fixed-term opportunity currently expected to run through March 2027.
- Interacts with various levels of management, international regulatory affairs/quality assurance, and global regulatory bodies on the adverse event reporting process.
Responsibilities
- Perform complaint investigations and assist with reporting decisions.
- Performs and reviews complaint investigations and makes recommendations for resolution.
- Maintains appropriate records for the Global Quality Assurance adverse event reporting system as defined in relevant procedures.
- Performs other duties and tasks, as needed.
Requirements
- Strong interpersonal skills and the ability to communicate well - verbally and in writing - with others.
Nice to have
- American Society for Quality (ASQ) Certifications - Certified Quality Auditor (CQA)
- Regulatory Affairs Certification - RAC (Global).
- Experience with electronic submissions.
- Computer skills/internet research
- Interpersonal/communication skills
- Quality system development/training
- Infectious Control Risk Category II:
- The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs.
Benefits
- Field of vision/peripheral
- Medical/Dental & Other Insurances (eligible the first of month after 30 days)
- 3 Weeks' Vacation | 1 Week Sick-Time | Paid Holidays
- 401K | Health Savings Account
- Low Cost Onsite Medical Clinic
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This listing is sourced directly from Merit Medical Systems's careers page and normalized into a canonical job model.