Regulatory Affairs Ectd Jobs

SciPro - , NJ, United States

Operational Leadership Qualifications: 10+ years of Regulatory Affairs experience Strong Regulatory Operations experience, specifically eCTD submissions Broad knowledge of CMC, Quality and Quality Operations

from: linkedin.com - 7 days ago

Thor Companies - , NJ, United States

their Regulatory Affairs team on a long-term contract. The ideal candidate will have 1-3 years of experience, hands-on experience with publishing submissions in eCTD format, ANDA and Biologics experience.

from: linkedin.com - 7 days ago

Insmed Incorporated - Bridgewater, New Jersey

projects to support the regulatory department as assigned. Provide support in software validation and migration activities relating to new or existing systems in Regulatory Affairs Required Skills 5 years

from: resume-library.com - 14 days ago

Scienta - , MA, United States

Regulatory Affairs Strategy (In Industry) experience Scientific of clinical expertise in Auto-Immune Disease IND, BLA Experience If you would like too find out more please reach out to Anthony.hughes

from: linkedin.com - 7 days ago

Brio Group - , NC, United States

licenses Preferred Qualifications: Bachelor’s Degree Required 3+ years of experience in Regulatory Affairs submissions Strong expertise in IND lifecycle management and submissions Skilled in Regulatory

from: linkedin.com - 10 days ago

Xeris Pharmaceuticals, Inc. - Chicago, Illinois

Overview: The Regulatory Publishing Specialist is responsible for the formatting, publishing (PDF), eCTD compilation, review, and dispatch of regulatory submissions to Health Authorities within

from: resume-library.com - 22 days ago

Cypress HCM - San Diego, CA, United States

; Regulatory Affairs Certification a plus Strong pharmaceutical Regulatory Affairs experience with a focus on drug/biologics development Direct experience in preparing, submitting, and managing global

from: linkedin.com - 9 days ago

Thermo Fisher Scientific - High Point, North Carolina, United States of America

, and GMP and publishing and submitting these in eCTD format to the FDA. Additionally, this position requires representation and advisory support to the Regulatory Affairs (RA) team in R&D project teams

from: jobs.thermofisher.com - 30 days ago

University of Colorado Anschutz - Aurora, United States

and at different stages of the product lifecycle. Strong experience with eCTD format. 3 years of experience working in cell and/or gene therapy field. Regulatory Affairs Certification (RAC) Knowledge, Skills

from: jobrxiv.org - More than 30 days ago