Senior Regulatory Specialist - Newark, DE

This role focuses on high-level coordination across several departments and functional areas to ensure all filing dates and requirements are satisfied. · ...

Our client is seeking a Senior Regulatory Specialist to lead regulatory and compliance filings from start to finish for both the New Jersey and Delaware Regulatory teams. · Lead regulatory and compliance filings from initiation to completion for regional regulatory teams. · Captu ...

We are seeking a Senior Regulatory Specialist to lead regulatory filings for our New Jersey and Delaware teams. This role involves coordinating across departments to ensure all filing dates are met. · Lead regulatory filings from initiation to completion. · ...

Our client is seeking a Senior Regulatory Specialist to lead regulatory and compliance filings from start to finish for both the New Jersey and Delaware Regulatory teams. · ...

The Regulatory Specialist is responsible for supplier certification and the maintenance and review of all documentation related to supplier and ingredient approval. · Serve as the primary administrator and key contact for the TraceGains platform. · Maintain complete and accurate ...

The Regulatory Specialist is responsible for supplier certification and the maintenance and review of all documentation related to supplier and ingredient approval for Chesapeake Spice Company's Supplier and Item Approval Programs. · Serve as the primary administrator and key con ...

The Regulatory Specialist is responsible for supplier certification and the maintenance and review of all documentation related to supplier and ingredient approval for Chesapeake Spice Company's Supplier and Item Approval Programs. Serve as the primary administrator and key cont ...

The Regulatory Specialist is responsible for supplier certification and the maintenance and review of all documentation related to supplier and ingredient approval for Chesapeake Spice Company's Supplier and Item Approval Programs. · This role works closely with suppliers, Procur ...

The Regulatory Specialist is responsible for supplier certification and the maintenance and review of all documentation related to supplier and ingredient approval for Chesapeake Spice Company's Supplier and Item Approval Programs. · ...

Supports necessary regulatory activities required for product market entry. · ...

The Sr. Specialist, Regulatory Affairs, Medical is responsible for influencing department regulatory processes and procedures, · Develop and implement medical device regulatory strategies for West's administration and safety system product portfolio with an emphasis on gaining re ...

The Principal Specialist is responsible for influencing department regulatory processes and procedures, developing strategies for worldwide regulatory approval, preparing global submissions including Premarket Notifications, Global Registrations, Technical Documentation for CE Ma ...

The Principal Specialist, Regulatory Affairs (Medical Devices) is responsible for influencing department regulatory processes and procedures, · developing strategies for worldwide regulatory approval, · preparing global submissions including Premarket Notifications, · Global Regi ...

The Sr. Specialist, Regulatory Affairs is responsible for influencing department regulatory processes and procedures developing strategies authoring reviewing and supporting global registrations including Premarket Notifications China NMPA Registrations Technical Documentation fo ...

This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week. · The Principal Specialist, Regulatory Affairs (Medical Devices) is responsible for influencing department regulatory processes and procedures, developing strategies for worldwide regul ...

The Recall Regulatory Specialist III will be responsible for leading OUS field action execution activities including managing Field Action Strategy Team meetings and coordinating document packages to notify regulatory agencies of field action activities. · ...

Job Summary · The Sr. Specialist, Regulatory Affairs, Medical is responsible for influencing department regulatory processes and procedures. · ...

+Job summary · The Sr. Regulatory Affairs/Quality Specialist is responsible for leading and assisting with various regulatory submissions, authoring, and editing regulatory documentation and procedures, and participating in compliance activities. · ...

The Regulatory Affairs Sr. Specialist is responsible for influencing department regulatory processes and procedures, developing strategies, authorizing reviews, and supporting global registrations including Premarket Notifications. · The Sr. · ...

The Post Market · Regulatory Affairs Specialist is responsible for supporting post market regulatory affairs activities associated with complaint handling and MDR submissions.The specialist will oversee and directly support technical evaluations and investigation tasks required ...