Merit Medical Systems

Merit Medical Systems

Post Market Surveillance Specialist (Fixed-Term)

Utah - Virtual, USA

Sponsorship not specifiedDetected 128 days ago
Project ManagementFDA RegulatoryPharmacovigilanceMedical DevicesResearchCommunicationTime ManagementRegulatory Affairs

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odds of building a lasting career here

37Risky
Cap-exempt (no lottery)0
Sponsors this role80
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

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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

Company info

  • Together, we are making a difference in the lives of patients around the world.

This listing is sourced directly from Merit Medical Systems's careers page and normalized into a canonical job model.