We are seeking a highly experienced and motivated Manager, Regulatory Affairs, to join our growing Regulatory Affairs team. This role is critical to ensuring compliance with US regulatory requirements and supporting the development, approval, and lifecycle management of medical devices. The ideal candidate will possess deep expertise in U.S. FDA regulations, and have a good general understanding of EU MDR, and international standards, and will contribute to strategic regulatory planning and execution. Responsibilities:
Lead regulatory strategy and submissions for Class II and III medical devices in the U.S.
Prepare and manage regulatory submissions including 510(k), PMA Supplements, annual reports
Serve as the US regulatory lead on cross-functional project teams, ensuring alignment with clinical, quality, and R&D functions.
Interpret and apply regulatory requirements to product development, labeling, and review of advertising and promotional materials.
Monitor changes in regulatory requirements and communicate impact to internal stakeholders.
Support audits and inspections by regulatory authorities.
Lead post-market regulatory assessments and submissions, including periodic reports, vigilance reporting, and regulatory renewals.
Manage complaint handling activities, ensuring timely investigation, documentation, and regulatory reporting in compliance with applicable standards.
Requirements:
Bachelor's degree in engineering, life sciences, pharmacy, or related field. Advanced degree preferred.
Minimum 10 years of experience in regulatory affairs within the medical device industry.
Proven track record of successful submissions to FDA
In-depth knowledge of FDA 21 CFR 820, ISO 13485, and other applicable standards.
Strong communication, leadership, and project management skills.
Experience with eQMS systems and electronic document control preferred
Numbers & Facts
Location
Mossville, IL
Skills
Advertisingunmatched
Biologyunmatched
Code of Federal Regulationsunmatched
Communication Skillsunmatched
Cross-Functionalunmatched
Document Controlunmatched
Documentationunmatched
FDA (Food and Drug Administration)unmatched
FDA Requirementsunmatched
Healthcare Qualityunmatched
ISO (International Organization for Standardization)unmatched
Interpret Regulationsunmatched
Leadershipunmatched
Maintain Complianceunmatched
Market Analysisunmatched
Medical Equipmentunmatched
Monitor Regulationsunmatched
Pharmacyunmatched
Product Developmentunmatched
Project/Program Managementunmatched
Regulationsunmatched
Regulatory Complianceunmatched
Regulatory Reportsunmatched
Regulatory Requirementsunmatched
Regulatory Submissionsunmatched
Research & Development (R&D)unmatched
Strategic Planningunmatched
Team Lead/Managerunmatched
Time Managementunmatched
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