Regulatory Affairs Ectd Jobs

PAI Holdings LLC - Parsippany, NJ, US

Science or technological field plus at least 3 years in Pharmaceutical, Regulatory Affairs, Regulatory Publishing, Quality or scientific background is required. ECTD publishing and/or SPL experience Regulatory Affairs Ectd Work careers...

from: ziprecruiter.com - More than 30 days ago

Exeltis - Florham Park, NJ, US

and international co-workers to achieve goals, and leading such groups with respect to regulatory affairs work. * Managing the organization, preparation and review of new ANDAs, amendments, supplements, annual Regulatory Affairs Ectd careers...

from: ziprecruiter.com - More than 30 days ago

driftwood grove - Somerset, NJ, US

Manager of Regulatory Affairs in Somerset NJ. Fast growing company with great management team. Good writing and communication skills are required CMC experience required Experience with ANDA/IND/NDA ectd...

from: jobvertise.com - 3 days ago

Garuda Therapeutics, Inc. - Cambridge, MA, US

QUALIFICATIONS * Bachelor's degree in a scientific discipline is required, advanced degree is preferred * A minimum of 8 years of experience in regulatory affairs with a focus on CMC documentation and CMC life regulatory operation ectd...

from: ziprecruiter.com - More than 30 days ago

Kezar Life Sciences - South San Francisco, California

to regulatory affairs (e.g., regulatory impact assessments for change management, regulatory inspection support). Drive a culture of continuous improvement to ensure compliance with Kezar standards, procedures regulatory submission publisher...

from: resume-library.com (+1 source) - 3 days ago

Abacus Service Corporation - Princeton, New Jersey

Description: Regulatory Affairs Operations Associate to support submission review, publishing in eCTD format and archiving for ANDAs, NDAs, sNDAs, INDs, DMFs, annual reports and safety reports regulatory operations specialist ectd ectd...

from: resume-library.com - 9 days ago

Enanta Pharmaceuticals, Inc. - Watertown, Massachusetts, USA

, or related pharmaceutical field preferred. • 12+ years of experience in the pharmaceutical, biotechnology or related industry. • 8+ years of experience in regulatory affairs CMC or a related ectd submissions specialist...

from: Ivyexec.com - 7 days ago

The Fountain Group LLC - Princeton, New Jersey

Contract Duration: 12+ months Pay Range: $44 - $58/Hour W2 Description Regulatory Affairs Operations Associate to support submission review, publishing in eCTD format and archiving for ANDAs, NDAs regulatory affairs ectd knowledge...

from: resume-library.com - 9 days ago

Katalyst Healthcares & Life Sciences - Santa Clara, California

the Regulatory Affairs with electronic submission to FDA by preparing the documents under CRT folder with compliance to eCTD guidelines. Reviews the programming and data management related documents, e.g., case control regulatory affairs ectd...

from: resume-library.com - 12 days ago

IQVIA - Berkshire, UK

and variation strategies Broad understanding of the requirements to place the products on the market within EU Experience with Regulatory Affairs and Microsoft Office software and databases (e.g. eCTD publishing

from: Pharmadiversityjobboard.com - 17 days ago