Job Description
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 change requests for 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 R & D, QA, Planning and Manufacturing teams.
How You'll Make An Impact:
- Strong prioritization skills, flexibility and ability to handle multiple projects simultaneously while meeting deadlines
- Ability to communicate effectively with employees across multiple departments
- Highly organized and detail-oriented. Good time management.
- Technical aptitude for understanding IVD product features
- Understanding ...
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