About this role
Regulatory Specialist at Globus Medical. Location: Audubon, Pennsylvania, United States. Role: preparing submissions, submitting filings, reviewing labeling Requirements: Prepare and submit FDA regulatory submissions (510(k), IDE, PMA), review labeling and documentation, coordinate with cross-functional teams; 2+ years regulatory affairs experience in medical device industry; bachelor’s degree or equivalent. Category: Research and Development (R&D) Seniority: Entry Level Tools: Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Teams Commitment: Full Time Workplace: Onsite Languages: English