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!
...position requires expertise in designing, developing, debugging, and maintaining AI-powered... ...Preferred qualifications include experience with retrieval-augmented generation (RAG... ...microservices, and automation. Build and maintain Python based AI services using lang Chain and...
...Position: 2nd Shift Forklift Operator / Warehouse Associate Salary: $22 per hour Hours: Monday-Friday, 3:00pm-11:30pm Location: Ayer, MA The leading provider of conventional, Non-GMO Project verified and organic oils to the ingredients, foodservice and retail...
...based on experience ~ Consistent M-F schedule, no overnights or weekends ~ Benefits including Healthcare About Our Client... ...experience (ability to perform without supervision)~ Ability to work on site M-F on site (there is no remote or hybrid days)...
...presentations. Presents to external groups outside of local department Skills & Qualifications: Masters Degree from an accredited Speech Language Pathology program. Must have attained or be eligible for Certificate of Clinical Competence. Bilingual in Spanish is...
..., team-oriented Licensed Practical Nurse (LPN) to provide quality, holistic care to patients... ...they are being heard. Our ambulatory LPNs work under the supervision of a Registered... ...generous time off package to maintain a healthy home-work balance. For more information about...