TRABAJO REGULATORY AFFAIRS MEDICAL DEVICE

Job qualifications required: ms preferred, bs or comparable required minimum of 5-7 years experience in regulatory affairs in medical device industry with focus...

Job qualifications required: regulatory affairs experience in the medical device industry is mandatory [minimum 10 years with bs/ba, or 7 years with ms preferred]...

Job description the business relationship manager (brm) will co-create, own, and drive the global it strategy for the assigned quality assurance and regulatory...

• knowledge of applicable clinical research regulatory requirements, i... we create intelligent connections to accelerate the development and commercialization of...

Liderar y coordinar con bsn medical cali la disponibilidad de todos los documentos requeridos para asegurar un proceso de registro, actualización o renovación exitoso...

Bsos ensure that all regulatory systems are effectively supporting global regulatory operations, compliance, and business objectives... why you?   basic qualifications:...

Moderate experience in regulatory... comprehensive regulatory knowledge and understanding of pharmaceutical and or medical device product development...

Job description position reports to head of therapy areas general medicine vaccines & specialities (gemvacs) as part of local medical affairs department...

The position reports to the director, global government affairs... the director will work with corning’s global government affairs staff, business units, and government...

Serve as a scientific, clinical, and medical content expert and partner within all areas of medical affairs (e... medical directors, medical communications, medical...

Knowledge of local and/or international regulatory processes, including submissions to regulatory authorities and ethics committees... maintaining accurate and up-to-date...

Develop an understanding of operational and financial aspects of a medical device business...   support sales team members in the operating room with imaging and...

We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population...

Coordinating with regulatory and cts on ca submission and approval status to assure alignment with other site activation requirements... we create intelligent connections...

We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities... job responsibilities •    responsible for...

Demonstrated working knowledge of medical device quality systems regulations including iso cfr820, and 21cfr803... basic knowledge of medical terminology and human...

This role ensures the delivery of high-quality, compliant, and timely regulatory reports that meet the business needs and regulatory requirements across various...