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!
...About the Company Meissner Sewing & Vacuum Centers is a family-owned business headquartered in Sacramento, California operating since 1930. Meissner offers sales and service of home sewing machines, industrial sewing machines and vacuums as well as a wide array of classes...
...Description Summary: The Ultrasound Technologist will perform a wide variety of routine and advanced imaging procedures, will provide support for other imaging technologists as needed, and help to facilitate smooth and efficient patient flow. The Ultrasound Technologist...
PIPEFITTERS WITH 4 YEARS OF JOURNEYMAN INDUSTRIAL EXPERIENCE. NCCER CERTIFIED PREFERRED BUT NOT REQUIREMENT MUST HAVE ALL JOURNEYMAN TOOLS. *MUST BE WILLING TO WORK AT HEIGHTS OF UP TO 300 FEET.* Physical Requirements: Climbing, Balancing, Stooping, Kneeling...
Project Description: Become part of the latest generation of HMI development. In the environment of the most attractive automobile manufacturer in Germany. Benchmark technologies in the area of AR/HUD will be defined here. Our team of experts accompanies development...
Were seeking a Production Assistant to support a contemporary fashion brands production team on a short-term freelance basis, with the potential to extend. This role is ideal for someone detail-oriented and proactive, looking to gain hands-on experience in apparel ...