Senior Manager, CMC Site Scheduling - Cell & Gene Therapy
Boston, Massachusetts
Vertex Pharmaceuticals Incorporated
Job Description General Position Summary: The Senior Manager for Site Scheduling is responsible for performing multiple activities in support of the T1 D program at Vertex Cell & Gene Therapy. The role applies proficiency in scheduling prod...
16d
| Job Type | Full Time |
Senior Director, Regulatory Labeling
Boston, Massachusetts
Vertex Pharmaceuticals Incorporated
Job Description General Summary: The Senior Director, Regulatory Labeling is regulatory labeling leader with expert technical and operational experience in regulatory labeling, globally, and is responsible for overseeing the development and...
16d
| Job Type | Full Time |
Director, Regulatory Strategy, Pain
Boston, Massachusetts
Vertex Pharmaceuticals Incorporated
Job Description General Summary: The Regulatory Strategy Director will be responsible for the development and implementation of innovative global/regional regulatory strategies for new product development within the Vertex portfolio. This p...
16d
| Job Type | Full Time |
Sr Director, Regulatory Affairs
Boston, Massachusetts
JOB TITLE: Sr. Director, Global Regulatory Affairs REPORTS TO: Vice President, Regulatory Affairs LOCATION: Boston MA DATE PREPARED: April 17, 2025 JOB SUMMARY: AVEO Oncology is seeking an experienced Senior Director, Regulatory Affairs who...
16d
| 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...
17d
| 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...
17d
| 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...
17d
| 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 ...
18d
| 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...
18d
| 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
18d
| Job Type | Full Time |