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!
...global theme park destinations, consumer products, and experiences. We own and operate leading entertainment and news brands, including NBC, NBC News, NBC Sports, Telemundo, NBC Local Stations, Bravo, and Peacock, our premium ad-supported streaming service. We produce and...
...touchpoint experiences. ~ Proficiency with modern UX design tools (Figma, Sketch, Adobe XD, etc.). ~ Excellent communication skills and comfort presenting to senior stakeholders. ~ Experience with experimentation, testing, and data-informed decision-making....
Electrician What it feels like to work at Jule: Jule has maintained its flat management structure and start-up culture, despite its steady growth in the industry for the past ten years. The Electrician will be a part of a rapidly growing operational team with opportunities...
...Superintendent Commercial General Contractor Location: Houston, TX A well-established Commercial General Contractor in Houston... ...operations team. This contractor specializes in ground-up commercial construction across healthcare, education, religious and government...
Work from Home Data Entry & Office Administration Flexible Online Role About the Job We are seeking organized and motivated individuals in Henderson, Kentucky, USA, for an entry-level remote position in data entry, office administration, and online research...