TRABAJO ASSOCIATE REGULATORY SUBMISSIONS
(175 ofertas de trabajo)
Listado de trabajos de Associate regulatory submissions
Associate director, cmc regulatory affairs
Johnson & johnson is recruiting for an associate director, cmc regulatory affairs... reviews cmc regulatory dossiers for global submissions throughout the product...
Associate director, regulatory affairs
Collaborate with global regulatory teams and the global regulatory affairs (gra) function/teams to facilitate regulatory activities... the associate director, regulatory...
Regulatory affairs associate - johnson & johnson medtech
Ability to author and submit us, eu and international regulatory submissions to regulatory bodies... partners with other functions to define and obtain data to assist...
Junior associate, regulatory operations & systems management
The role reports to the associate director, regulatory operations & systems management... specific responsibilities regulatory systems compliance and managementensure...
Regulatory manager, clinical trials regulatory management- home-based, emea
Prepares and/or reviews regulatory documents to support clinical trial submissions... independently provides regulatory support for complex projects and programs...
Associate director, regulatory medical writing
Maintains and disseminates knowledge of industry, company, and regulatory guidelines... we are recruiting for an associate director to join the regulatory medical...
Technical regulatory associate
Preparare la documentazione di registrazione locale in collaborazione con il regulatory affairs di janssen-cilag, milano... preparare la documentazione di registrazione...
Senior associate/specialist, regulatory intelligence and analytics
Chance to build a broad and comprehensive knowledge on phv processes and requirements chance to expand knowledge on other areas covered by regulatory and clinical...
Regulatory affairs associate temporary
Organizes regulatory information, logs and tracking... maintains regulatory files/database and chronologies in good order... participate in the product development...
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Associate director, business analyst, ddit dev., regulatory affairs
Experience in regulatory affairs business processes is a plus (e... we are looking for an experienced individual in global drug development regulatory affairs to...
Regulatory affairs specialist ii (sports orthopedics) - medical device business services, inc.
Experience in worldwide regulatory systems preferred... the regulatory affairs specialist ii provides regulatory guidance to project teams in business planning and...
Experience with the preparation and approval of regulatory submissions for brand name prescription drugs to a major regulatory authority (e... msc/phd preferred...
Cmc regulatory affairs director
Strong understanding of regulatory affairs globally direct regulatory affairs cmc experience with submissions for synthetics and/or biologic and biotechnology...
Cmc regulatory affairs manager
Develops and builds expertise in regional regulatory requirements to ensure assurance of compliance of cmc submissions... they project manage global cmc regulatory...
Director, global regulatory leader (grl)
Global regulatory experience is required for the grl role... the director, global regulatory leader, is responsible for global regulatory strategies for select projects...
Director, regulatory operations
Proven track record of successful regulatory submissions and approvals... manage regulatory submissions and timelines, ensuring accuracy and completeness of documentation...
Senior study start up associate
Strong understanding of regulatory requirements and guidelines for clinical trials, including ich-gcp and local regulatory requirements... in addition to your competitive...
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