The Sr. CMC Regulatory Affairs Specialist performs regulatory assessment of changes. Interpreting the current, approved and planned clinical regulatory landscape by contributing to the regulatory submission form process. A typical...
Since its inception in 2014 by pioneering Bitcoin enthusiasts, Tether has not only launched the first 'stablecoin', USDT, but also expanded its horizons into Tether Data, Tether Power, Tether Edu, and more. Our platforms and tokens...
Hobson Prior is seeking a motivated Senior Regulatory Affairs Specialist focused on device development. The successful candidate will ensure regulatory compliance and support the development and commercialization of innovative medical devices.
With the Senior Vice President, Government Affairs, manages State governmental affairs for FINRA. The position serves as a central point of contact between FINRA, state financial services regulators and the North American Securities Administrators...
About My Client My client is at the forefront of oncology innovation, particularly in hematology and oncology, to improve outcomes for patients with relapsed or refractory cancers. With a robust intellectual property...
Aptar is a leader in the development and manufacture of dosing, delivery, closure, and protection systems for the pharmaceutical and consumer industries. With 3 Business Segments, Pharma, Beauty and Closures, Aptar has a turnover of $3.5 billion...
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,...
This position, under the direction of the Executive Director, supervises and manages the Regulatory Programs Division.The position includes but is not limited to being responsible for the leadership and management of the Division, including budget...
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.