Strong data validation and quality control mindset
This role combines operational execution with applied regulatory knowledge to translate complex registration and financial data into clear insights for cross-functional partners
Job Summary
This role combines operational execution with applied regulatory knowledge to translate complex registration and financial data into clear insights for cross-functional partners.
The position is responsible for global MDS dashboard creation, weekly regulatory reporting, and supporting prioritization of international submissions to align with business goals.
Candidates must have a minimum of 5 years in data management or related disciplines, with preferred experience in regulatory affairs within the medical technology sector.
Matching Summary
This role combines operational execution with applied regulatory knowledge to translate complex registration and financial data into clear insights for cross-functional partners.
Salary
Base: $106,600.00 - $175,900.00 USD Annual; Bonus/Equity: Not specified; Benefits: Comprehensive Total Rewards program including performance-based culture and competitive package
Skills & Requirements
Must-have
Advanced Power BI and Excel skills
Experience with large regulatory datasets
Strong data validation and quality control mindset
Ability to analyze trends and inconsistencies
Microsoft Office 365 proficiency
Nice-to-have
International medical device submission lifecycle knowledge
Cross-functional communication without direct authority
Proactive risk escalation and diplomatic problem solving
Understanding of market access and revenue implications
Operational excellence in repetitive reporting cadences
Key Requirements
Minimum BA/BS in technical or scientific discipline
Minimum 5 years of data management experience
Preferred 2 years of regulatory affairs experience