TRABAJO REGULATORY AFFAIRS MEDICAL DEVICE
(84 ofertas de trabajo)
Listado de trabajos de Regulatory affairs medical device
Global lead, medical affairs, respiratory job details | olympus corporation of the americas
The glmar is part of the growing medical affairs division within the broader medical and scientific affairs (msa) of olympus... posting notes: || united states...
Global lead - medical affairs, gastroenterology job details | olympus corporation of the americas
) comprehensive medical affairs proficiencies (e... active medical license... the glmag is part of the growing medical affairs division within the broader medical...
Has a broad understanding of the global medical device regulatory landscape, regulatory submissions (e... job description the senior specialist, regulatory affairs...
Senior regulatory affairs specialist with experience in clinical trials
Proven ability to manage regulatory submissions and interactions with regulatory agencies... minimum of 2 years of experience in regulatory affairs within the pharmaceutical...
Medical affairs manager fixed term (1-year)
medical affairs manager fixed term (1-year) live what you will do let’s do this... proven ability as a medical expert in a complex matrix environment...
regulatory affairs analyst your task and responsabilities support to the regulatory affairs area in the preparation and submission of dossiers for...
Regulatory affairs manager (barcelona)
Arthada, a leading company in offering specialised hr services to the pharmaceutical sector, is recruiting for an international pharmaceutical company focused on...
Brm, quality assurance and regulatory affairs job details | olympus corporation of the americas
Job description the business relationship manager (brm) will co-create, own, and drive the global it strategy for the assigned quality assurance and regulatory...
Regulatory affairs associate ii - job details | teva pharmaceuticals
The opportunity to lead and proactively manage all regulatory activities associated with development, registration and maintenance of drug master files according...
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• knowledge of applicable clinical research regulatory requirements, i... we create intelligent connections to accelerate the development and commercialization of...
Senior manager, development and regulatory operations
Bsos ensure that all regulatory systems are effectively supporting global regulatory operations, compliance, and business objectives... why you? basic qualifications:...
A minimum of 12 years of experience in healthcare, pharmaceutical and/or medical device industry... posting notes: || united states (us) || massachusetts (us-ma)...
Understanding of technology security and regulatory requirements... domain architecture assist in the integration of technology solutions across research and development...
Manager of medical content, global job details | olympus corporation of the americas
Posting notes: || united states (us) || massachusetts (us-ma) || westborough || medical affairs ... assuming responsibility for the incorporation of the medical...
Associate medical director (vaccines)
Job description position reports to head of therapy areas general medicine vaccines & specialities (gemvacs) as part of local medical affairs department...
Director, government affairs, mexico
The position reports to the director, global government affairs... the director will work with corning’s global government affairs staff, business units, and government...
Senior medical science liaison – respiratory (guadalajara/ monterrey)
Serve as a scientific, clinical, and medical content expert and partner within all areas of medical affairs (e... medical directors, medical communications, medical...
Senior medical science liaison – oncology
Adhere to gsk policies and procedures for msl and medical affairs, supporting the safe and appropriate use of research compounds and products, and partnering with...
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