Leads the Chemistry, Manufacturing, and Controls (CMC) non-antibody team for cell and gene therapy technologies. The candidate will be responsible for assuring development and execution of global regulatory strategies for assigned cell and gene...
DIRECTOR, GLOBAL REG AFFAIRS STRATEGY LEAD - ONCOLOGY Growing $1.5Bn+ revenue, $7Bn market cap, 550-person biotech1 approved cancer blockbuster with 1 anticipated blockbuster in late...
**_What Regulatory Affairs and Clinical Submissions contributes to Cardinal Health_** The _Manager, Regulatory Affairs (Clinical Submissions)_ is responsible for ensuring compliance with regulatory requirements for clinical trials and...
About J2 Health: At J2 Health, we know that healthcare is complicated and falls short of what consumers deserve. J2 wants to change that by focusing on transforming a critical and underserved part of the healthcare ecosystem-...
Job Summary: This position is vital to ensuring the timely and high-quality delivery of the carve-out project, making a significant impact on the overall success of the regulatory affairs team. Key...
Job Description Hiring a Director of Regulatory Affairs - Lead the Charge in Compliance and Excellence Are you ready to make a significant impact at a full-service medical center and teaching hospital in the...
Summary Client is a leading company in lifestyle and culture that helps our customers realize their beauty and dreams. We share our core values Beautiful, Healthy, and Refreshing with our customers. As a...
Senior Director of Regulatory Affairs Job Ref: 112166 Category: Professional Department: OFFICE CORPORATE COMPLIANCE Location: 50 Water Street, 7th Floor, New York, NY 10004 Job Type: Regular Employment Type:...
Part of the Interparfums group founded in 1982, Interparfums USA develops, manufactures and distributes prestige perfumes and cosmetics as the exclusive worldwide licensee for Abercrombie & Fitch, Anna Sui, DKNY, Donna Karan, Dunhill, Graff,...
The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area.