Regulatory Affairs Specialist - Creedmoor, NC, US

The Regulatory Affairs Specialist is responsible to develop and execute the regulatory strategy for new product development, design changes, and field safety corrections, · Author EU MDR technical files and will contribute to other international regulatory submissions. · Particip ...

Job summaryThe Regulatory Affairs Specialist is responsible to develop and execute the regulatory strategy for new product development... · ...

We are seeking a Regulatory Affairs Specialist to support regulatory submissions lifecycle management compliance activities for pharmaceutical medical device products. · This is a W2 contract role supporting ongoing regulatory operations in a fast-paced GxP environment. · Prepare ...

We are seeking a Regulatory Affairs Specialist to support regulatory submissions lifecycle management and compliance activities for pharmaceutical or medical device products. · 2–5+ years of Regulatory Affairs experience (Pharma Biotech or Medical Devices) · Strong knowledge of F ...

The Regulatory Affairs Specialist will be responsible for a wide variety of regulatory activities for sustaining products including medical devices and Software as Medical Device (SaMD) and regulatory operation. · ...

Perform assessment of CMC changes, identifying global regulatory requirements. · ...

Teleflex is investing in our capability to drive material cost improvement opportunities as part of a strategic corporate approach to reversing recent trends in cost escalation and generating significant stakeholder value. · ...

Teleflex is investing in our capability to drive material cost improvement opportunities as part of a strategic corporate approach to reversing recent trends in cost escalation and generating significant stakeholder value. · ...

Teleflex is investing in our capability to drive material cost improvement opportunities as part of a strategic corporate approach to reversing recent trends in cost escalation and generating significant stakeholder value. · ...

Developing global regulatory submissions for medical device industry with EU MDR experience required. · ...

· The Specialist supports the coordination and delivery of public affairs, stakeholder engagement, community relations, and communications activities across Carnival Corporation's global destination portfolio. · This role requires addressing complex operational challenges in a d ...

++This position performs specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for regulatory approval. · +++Prepares robust regulatory applications to achieve departmental and organizational objectives. · Creats reviews and ...

This is an administrative contract role responsible for providing essential operational and coordination support within a Medical Affairs function.The position focuses on processing and tracking contracts, purchase requests, purchase orders, and invoices. · ...

This is an administrative contract role responsible for providing essential operational and coordination support within a Medical Affairs function. · ...

This is an administrative contract role responsible for providing essential operational and coordination support within a Medical Affairs function. The position focuses on processing and tracking contracts, purchase requests, purchase orders, and invoices. · The role is well suit ...

Independently manage essential regulatory documentation for submission to country/regional/site Institutional Review Boards (IRB), Ethics Committees (EC), Competent Authorities (CA) and/or other Regulatory Bodies for all clinical studies performed globally. Assist/Advise project ...

This position will independently manage essential regulatory documentation for submission to country/regional/site Institutional Review Boards (IRB), Ethics Committees (EC), Competent Authorities (CA) and/or other Regulatory Bodies. The Regulatory Affairs Specialist will interact ...

Corrections professionals who foster a humane and secure environment and ensure public safety by preparing individuals for successful reentry into our communities. · ...

This position will provide information and guidance to students and others regarding the VA Educational benefits process while ensuring compliance with the Department of Veterans Affairs (DVA). · Serves as a VA School Certifying Official for veteran students receiving Federal GI ...

+The Associate Regulatory Affairs Manager will support the development review and submission of regulatory documents for medical devices and IVD products. · +The Associate Regulatory Affairs Manager will support the development review and submission of regulatory documents for me ...