+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 Director of Quality & Regulatory is responsible for oversight execution and continuous improvement of the company's Quality Management System across all functions suppliers and manufacturing partners leading and executing global domestic regulatory strategy filings compliance ...

Piper Health and Sciences is actively seeking a Quality Assurance Specialist – Supplier Quality to work for a large global biotechnology company. · ...

+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. · ...

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. · PharmD degree required · Minimum of 3 years ...

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 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 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 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 Mortgage Quality Assurance Specialist is responsible for ensuring compliance with internal policies and regulatory guidelines throughout the mortgage origination and servicing process. · Conduct 100% review of loan files and prepare and submit HMDA data reporting monthly to t ...

The Mortgage Quality Assurance Specialist is responsible for ensuring compliance with internal policies and regulatory guidelines throughout the mortgage origination and servicing process. · ...

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 ...

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 Quality Improvement Specialist conducts incident reviews and ensures compliance with external incident reporting requirements.This position takes the lead on conducting investigations in a timely, thorough and objective manner and in accordance with all regulatory requirement ...

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 ...

The company is seeking a Medical Quality Assurance Specialist on their Veteran Affairs Services team. You will work closely with medical providers and the Veterans Administration to ensure the documentation process is complete and accurate. · Review and audit exam reports sent ov ...

The Quality Specialist is responsible for ensuring that a product meets specific requirements for the company and its customers.The Quality Specialist may also handle customer complaints, investigate nonconformances and address any daily quality issues with other staff. · ...