Medical Device - Regulatory/Compliance Specialist (6 months)
Peoplemark, Inc - Memphis, TN

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Medical Device - Regulatory/Compliance Specialist

IMMEDIATE NEED
LONG TERM (6 mo) ASSIGNMENT.

Qualifications

  • Experience within medical device adverse event area
  • Familiar with time tables of filing FDA MDR reports and complaint handling.
  • Must have excellent written and verbal communication skills
  • Expertise dealing with Chief Medical Officer and physicians.
  • SAP experience and big plus with recall coordination background.

Responsibilities

  • Primary function will be to handle information from complaint investigations.

Hourly rate will depend on exp and education.
Only qualified individuals need apply.

Medical Device - Regulatory/Compliance Specialist


Indeed - 17 months ago - save job
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