Sr Manager, Regulatory Operations - Publishing & Registration Management (Devices)

In this role, a typical day will include:

• Oversee multiple regulatory operations projects, ensuring goals are met through effective management and oversight in support of medical device and/or pharmaceutical products
• Lead teams responsible for dossier preparation, Clinical Trial Disclosure, submission management, submission publishing, licensing, and labeling, ensuring timely and accurate submission of regulatory documents
• Make key decisions impacting project performance and success
• Apply project management, advanced problem-solving, effective communication, leadership, and industry-specific knowledge
• Adhere to Good Practice (GxP) regulations by following Standard Operating Procedures (SOPs), maintaining accurate documentation, and ensuring quality control
• Commit to continuous improvement and compliance with regulatory requirements

Preferred Qualifications/Skills/Experience:

• Demonstrate deep expertise in the regulatory submission lifecycle and associated processes for Class I, Class II, and Class III medical devices across the United States, European Union, and Canada
• Possess comprehensive knowledge of key regulatory submission platforms and portals, including the U.S. Food and Drug Administration (FDA) electronic Submission Template and Resource (eSTAR), Health Canada Regulatory Enrolment Process (REP), and European Union Notified Body submission portals.
• Experienced in managing export certification activities through the Center for Devices and Radiological Health (CDRH) Export Certification Application and Tracking System (CECATS), including Certificates to Foreign Government (CFG), Certificates of Exportability (COE), and European Union Free Sale Certificates (FSC).
• Lead the optimization and standardization of apostille, notarization, legalization, and country-specific documentation processes to support international regulatory submissions, accelerate approval timelines, and improve operational efficiency.
• Serve as a subject matter expert on global registration and submission pathways, providing strategic guidance for regulatory submissions and market access activities across the U.S., EU, Canada, and international markets.
• Identify and implement process improvements that reduce submission cycle times, enhance compliance, and improve the quality and consistency of regulatory documentation.