Are you a Regulatory Affairs professional looking to work independently and take ownership of the writing of CMC sections of DMF, BLA, and NDA submissions? Have you supported full product development activities from pre-clinical/clinical to FDA submissions? Are you interested in helping a company expand their client base in new countries? Do you have experience independently writing CMC sections of global regulatory submissions? This position could be for you!
If you're interested in a Lead Regulatory Affairs Specialist position with a well established pharmaceutical company in Madison, Wisconsin, apply here for more details!
Company Description Boyd Gaming Corporation has been successful in gaming jurisdiction in which we operate in the United States and is one of the premier casino entertainment companies in the United States. Never content to rest upon our successes, we will continue ...
...pass United States Department of Homeland Security background check to obtain a Transportation Worker Identification Credential (TWIC) card. Working knowledge of Microsoft Outlook, Word and Excel. Pass Forklift training and able to safely operate a forklift. Able...
...Job Title: Java Full Stack Developer (UI 70% / Backend 30%) Location: Dallas, TX Duration: Long Term Job Description: ~ Experience in Telecom Industry is a Must Front-End (UI) 70% Design and develop responsive, high-performance web interfaces using...
We're looking for an Order Processing Coordinator to join a growing team in Boca Raton. In this role, you'll handle order entry, shipment coordination, and account support to keep operations running smoothly. It's a great opportunity for someone with customer service or...
...Operator Location: Indianapolis, IN 46204 Openings: 10 total openings Schedule: Panama Shifts (3 on, 2 off | 2 on, 3 off) Hours: We have openings for both day and night shift (see hours below) Day Shift: 5:45am EST - 5:45pm EST Night Shift: 5:45pm EST - 5:...