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!
Key member of the marketing team responsible for managing the digital marketing programs to support the retail, at-home, and ecommerce business units. He/she will help manage the paid search, email marketing, social media and other digital programs that are important part...
...in the lives of children. If this is you, this opportunity is for you! Job Summary: Diagnoses and treats individuals with speech, language, swallowing, voice and fluency impairments. Performs speech and language examinations to learn the patient's degree of impairment...
...that the opportunity to learn is exponential. The majority of your time spent with us will be 1:1 training and mentoring, which will... ...to success is empowering our people. Who Should Apply: Students pursuing a degree in Construction Management Strong communicators...
...role: The primary accountability of this role is to ensure client success by leading, planning, and executing a broad portfolio of development projects. This includes oversight of formulation and process development activities from pre-formulation through clinical batch...
...Title: Manufacturing Engineer Location: West Columbia, SC Hire Type: Contract to Hire Shift: 1st Shift Pay Range: Starting at $32/hr - depending on experience Benefits: Insurance (Health, Medical, Dental), PTO, and more! We are seeking a highly skilled...