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!
...or early-career professional interested in learning more about legal and people operations within a global esports organization? Do... ...and want hands-on exposure to how contracts, documentation, and internal processes are managed? If so, you could be a great fit for the...
...to meet the needs of the business and performance requirements. Excellent phone etiquette and excellent verbal, written, and interpersonal skills Ability to multi-task, organize, and prioritize work experience in a contact center environment preferred....
...ABOUT HUDSON HEALTH Hudson Health (Medical + Mind + Life), was established in 2010 as a modern, fully integrated medical practice... ...over the course of 12+ years treating 50K patients. Medical Assistant Position Hudson Health is currently searching for a...
Project Manager (Mechanical Contractor) Company Description: E. Escher Incorporated is a Georgia based mechanical contractor incorporated in 1990. We selfperform installation of piping, chillers, AHU, cooling towers, pumps, etc., and subcontract sheet metal, insulation...
...platform-specific audiences (e.g., Amazon, Instagram, Walmart) Collaborate with marketing and creative teams to generate ideas and campaign messaging Research target audiences and products to craft compelling selling points Content Performance & Optimization...