Regulatory Affairs Specialist (remote)

Marquee Staffing
CA, US
$20-$22 an hour
Remote
Temporary
Quick Apply

Medical manufacturer is hiring a Regulatory Affairs Specialist on a temporary basis. This is a 6-month contract working 100% remote.

You will be responsible for submitting change notifications, and updating documentation changes to legal entities.

Schedule : Monday thru Friday 8am to 4 : 30pm

Compensation : $20-22 / hr

  • Submit change notification to multiple Notified Bodies
  • Submit change notification to both EU Authorized Reps
  • Submit Change notification to all international Authorized Reps
  • Submit change notification to all international Distributors
  • Update Technical Documentation for address and manufacturing changes of 2 legal entities The more detailed requirements of these activities are below;
  • Work cross functionally to draw up details of manufacturing and address changes
  • Track and follow-up communication with all international Distributors and Authorized Reps
  • Update international licenses as required by international Distributors and Authorized Reps
  • Review and approve Change Orders regarding manufacturing and address changes for both businesses
  • Represent RA in Project Safari meetings
  • Update clinical, post-market, summary of technical documentation and input any new documents from cross-functional teams into Technical Documentation
  • Submit Label Checklists to labeling team
  • Reserve and apply new UDI for address and manufacturing changes
  • Track and follow-up communication of changes with all State License bodies for both businesses Qualifications / Requirements
  • Must have experience using Office 365; Outlook, Word, Excel and Access
  • Must work independently and productively with minimal supervision
  • Previous medical device experience in a Regulatory Affairs capacity
  • Previous experience registering medical devices internationally and the EU
  • Great understanding of FDA CFR relating to med device and med device registration
  • Previous experience drawing up med device Technical Documentation
  • Preferred experience with state licensing bodies
  • Strong attention to detail
  • Enthusiastic about learning
  • Self-Motivated and team player
  • Critical thinking & Analytical skills
  • 19 days ago
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