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Associate Director, Regulatory Labeling Strategy (Remote)
Boston, Massachusetts
Vertex Pharmaceuticals Incorporated
Job Description General Summary: The Regulatory Labeling Associate Director will be responsible for strategic development of global labeling (CCDS, USPI, EU SmPC and other markets as necessary) on one or more marketed products. This role ma...
12d
| Job Type | Full Time |
Sr Director, Regulatory Affairs
Boston, Massachusetts
JOB TITLE: Senior Sales Operations Analyst LOCATION: Seaport, Boston, MA (hybrid 3 days in office) DEPARTMENT: Business Analytics DATE PREPARED: 04/22/2025 JOB SUMMARY: The Senior Sales Operations Analyst will aid the continued success of f...
12d
| Job Type | Full Time |
Senior Manager, CMC Radiopharmaceuticals
Paramus, New Jersey
Senior Manager, CMC Radiopharmaceuticals Job Locations US-NJ-Paramus ID 2025-1895 Category CMC Type Regular Full-Time Overview The Senior Manager, CMC, Radiopharmaceuticals (RPT) will be working on CMC aspects for SK Life Science Inc.'s RPT...
12d
| Job Type | Full Time |
Associate Director, CMC Regulatory Affairs
Foster City, California
Position Summary The Associate Director of CMC Regulatory Affairs provides support for all CMC regulatory activities related to the ongoing development, registration, and life-cycle management of RYTELO (imetelstat) and other potential futu...
12d
| Job Type | Full Time |
Regulatory Affairs Operations Senior Manager
Foster City, California
Position Summary The Regulatory Affairs Operations Senior Manager is responsible for the accurate and efficient execution of the Company's end-to-end submissions process as well as the maintenance of product data within the Company's Regula...
12d
| Job Type | Full Time |
Director, Vaccine Mature Products, CMC
Durham, North Carolina
Site Name: Italy - Siena, Belgium-Wavre, UK - London - New Oxford Street, USA - North Carolina - Durham Posted Date: Apr 30 2025 Director, Vaccine Mature Products, CMC Location: Siena, Italy / GSK HQ, UK / Wavre, Belgium / Poznan, Poland Di...
13d
| Job Type | Full Time |
Pharmacovigilance Quality Assurance Lead
Kalamazoo, Michigan
Role Description As the Pharmacovigilance (PV) Quality Assurance Team Lead within the Regulatory Affairs, Global Quality & Compliance (GQC) group, oversee the Quality Assurance (QA) PV program for Zoetis. Continuously develop and drive the ...
13d
| Job Type | Full Time |
Director, Quality Assurance/Regulatory Affairs, Hoxworth Blood Center
Cincinnati, Ohio
Director, Quality Assurance/Regulatory Affairs, Hoxworth Blood Center Current UC employees must apply internally via SuccessFactors Founded in 1819, the University of Cincinnati ranks among the nation's best urban public research universiti...
14d
| Job Type | Full Time |
(Senior) Regulatory Affairs Consultant /
King of Prussia, Pennsylvania
Parexel International Corporation
PMDAMHLW NDA 1. * NDA * USEU * * PMDAPMDAPMDA * NDACTDNDA * ODD 2. * * * * * * CRO10 * PMDAJNDACTD * PMDA * * * * Microsoft ExcelWordPower Point
14d
| Job Type | Full Time |
Regulatory Affairs Professional - CTA
King of Prussia, Pennsylvania
Parexel International Corporation
We are recruiting for experienced Regulatory Affairs Professionals on various levels. In this role, you will focus on clinical trial submissions. We are looking for someone who is experienced in CTA, EU-CTR knowledge and experience would be...
14d
| Job Type | Full Time |