Regulatory Affairs Specialist - Wilmington

Job summary: Regulatory Affairs Specialist to join one of our growing Medical Device clients in Audubon, PA. · ...

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 ...

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

IntePros is currently looking for a Sr. Regulatory Affairs Specialist to join one of our growing Medical Device clients in Audubon, PA. · ...

IntePros is currently looking for a Lead Regulatory Affairs Specialist to join one of our growing medical device/manufacturing clients in Audubon, PA. · ...

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, ...

The Abramson Cancer Center (ACC) of the University of Pennsylvania is a world leader in developing and conducting innovative clinical trials for the prevention, diagnosis, and treatment of cancer. · ...

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 ...

The Regulatory Affairs Specialist is responsible for preparing, reviewing, and maintaining regulatory submissions and documentation required for US FDA approvals of high-risk medical devices. · ...

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 Abramson Cancer Center at the University of Pennsylvania seeks a full-time Regulatory Affairs Specialist-CC to participate in coordinating Phase I-V clinical trials. · ...

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. · ...

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 ...

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

At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a cultu ...

+We move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. · ...

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. · ...

+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 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 ...