Senior Regulatory Affairs Specialist - West Chester, PA

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 ...

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 ...

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 ...

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

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 ...

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 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 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 Regulatory Affairs Sr. Specialist is responsible for influencing department regulatory processes and procedures. · The position includes supporting internal and external customer regulatory requests. · Bachelor's with 5+ years of medical device, pharmaceutical or regulatory e ...

This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week. The Medical Affairs Specialist at West is a global function dedicated to supporting the company's clinical activities and aligning with strategic goals to maintain high standards for pa ...

+The Medical Affairs Specialist at West is a global function dedicated to supporting the company's clinical activities and aligning with strategic goals to maintain high standards for patient safety and support regulatory obligations. · ...

The Medical Affairs Specialist at West is a global function dedicated to supporting the company's clinical activities and aligning with strategic goals to maintain high standards for patient safety and support regulatory obligations. · PharmD degree required · Minimum of 3 years ...

+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. · ...

This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week who evaluates supplier regulatory declarations for compliance authors and maintains material compliance certifications and responds to internal and external customer and/or agency regula ...

We have an incredible opportunity for a Scientific Affairs Specialist II to join ICON's Scientific Affairs team.This role assists in scientific knowledge and expertise across assay technologies, laboratory services, and clinical trial applications. · ...

The Abramson Cancer Center (ACC) of the University of Pennsylvania seeks a Regulatory Affairs Specialist-CC to coordinate Phase I-V clinical trials. · Prepare and process all regulatory documentation through IRB, CTSRMC, FDA. · Organize and maintain regulatory affairs documentati ...

We have an incredible opportunity for a Scientific Affairs Specialist I to join ICON's Scientific Affairs team.The role assists in scientific knowledge and expertise across assay technologies, laboratory services, and clinical trial applications. · ...

We have an incredible opportunity for a Scientific Affairs Specialist I to join ICON's Scientific Affairs team. The role assists in scientific knowledge and expertise across assay technologies, laboratory services, and clinical trial applications. · ...

The Abramson Cancer Center (ACC) of the University of Pennsylvania seeks a full-time Regulatory Affairs Specialist-CC to participate in the coordination of Phase I-V clinical trials. · The successful candidate will prepare and process all regulatory documentation through the IRB, ...