Regulatory Affairs Ectd Jobs

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Senior RA/Medical writer  

Remegen Biosciences - Rockville, Maryland

Were seeking a highly motivated, self-driven, and enthusiastic Regulatory Affairs writer to join our Regulatory Affairs Team. At RemeGen, our regulatory affairs group is responsible for drafting Regulatory Affairs Ectd Work careers...

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from: resume-library.com (+1 source) - 17 days ago

Senior Regulatory Affairs Manager  

Remegen Biosciences - Rockville, Maryland

(MS, MD, PharmD, PhD, etc.) in life science discipline, biological science, clinical research or any other healthcare field and 3 years of experience with regulatory affairs pharmaceutical Regulatory Affairs Ectd careers...

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from: resume-library.com (+1 source) - 17 days ago

Senior Manager, Regulatory Affairs CMC  

PTC Therapeutics, Inc. - South Plainfield, NJ

as a liaison between the Regulatory Affairs team and other PTC departments under supervision of the Regulatory Affairs – CMC management. The Senior Manager, Regulatory Affairs - CMC ensures adherence to relevant ectd...

from: PTC Therapeutics, Inc. - 4 days ago

Senior Manager, Regulatory Submissions (Remote)  

Amicus Therapeutics - Princeton, New Jersey

in the Vault Regulatory Information Management (RIM) system. They act as subject matter expert for producing a dossier based on submission strategy, and ensure compliance to required format (i.e. eCTD, NEES regulatory operation ectd...

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from: resume-library.com - 18 days ago

Regulatory Affairs Associate  

United Therapeutics - Blacksburg, Virginia

%. Preferred Qualifications - MS or Ph.D. in biochemistry, microbiology, virology, or epidemiology. - At least 3-years direct experience with regulatory affairs. - Background and experiences in infectious regulatory submission publisher...

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from: resume-library.com - 19 days ago

Senior Manager/Associate Director, Regulatory Affairs  

Novavax - Gaithersburg, MD, USA

: Bachelor's degree preferably in a scientific field; advanced degree desirable. A minimum of 8-10 years in the biotechnology industry with at least 6 years in Regulatory Affairs. Demonstrated understanding regulatory operations specialist ectd ectd...

from: applicantpro.com - 4 days ago

Senior Associate, Regulatory Operations (Remote)  

Amicus Therapeutics - Princeton, New Jersey

Experience Requirements - 1-2 years of Regulatory Affairs Operations experience with drugs and/or biologics - Experience using Veeva Vault Regulatory Information Management (RIM) or other RIM systems, Document ectd submissions specialist...

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from: resume-library.com - 21 days ago

Consultant - Regulatory Process Management - R&D  

Veeva Systems - Montchanin, Delaware

Register, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, CARA, Extedo eCTD Manager, Trackwise, or other regulatory information management systems or publishing tools. Consulting experience regulatory affairs ectd knowledge...

from: snapjobsearch.com - 17 days ago

SENIOR ASSOCIATE, REGULATORY OPERATIONS  

Vir Biotechnology, Inc - San Francisco, CA

, NeeS). Track regulatory commitments for assigned products and work with Regulatory Affairs to ensure routine and periodic reporting requirements are met. Provide subject matter expertise control regulatory affairs ectd...

from: Pharmadiversityjobboard.com - 18 days ago

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Senior Pharma Medical Writer  

Catalyst Careers - Baden-Würrtemberg

brochures, clinical modules of the eCTD for submission dossiers in Europe, Asia and USA, interacting with the teams from Clinical Development, Regulatory Affairs and Pharmacovigilance. Posting of clinical

from: staffingfuture.com - More than 30 days ago


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