RA Specialist I - Jackie
Hybrid after 30 days Mondays and Tuesdays on site, the third day candidate’s choice. 8:00 to 4:30 however we are flexible. Experience in IVD medical device industry. is required
1 yearn - $40/hour pay
Provide regulatory support for IVD products with multiple product groups with clinical diagnostics. Assembles low to medium complexity regulatory submissions to support world wide product registration. IVDR Technical file maintenance and monitoring of change requests. Process improvements for SOPs related to full transition to IVDR. Basic analytical, communication, problem solving, and critical thinking skills to meet daily job responsibilities. Interface daily with desktop publisher, technical writers and regulatory specialists. Work collaboratively with Marketing, R & D, QA, Planning and Manufacturing teams.
How You'll Make An Impact:
What You Bring:
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