Featured Job
-
Job Removed or Not Found
Related Jobs
- Merck & Co. (Durham, NC)
- …Human Papilloma Virus ( HPV) Operations Manager, Training Center Durham's DS4 Operations Training Center Manager will be responsible for leading and executing Operations
- Catalent (St. Petersburg, FL)
- …Petersburg site. The Department has the responsibility for Quality aspects related to Quality Systems, Finished Product Batch Release, Change Control, Client interface,
- Novo Nordisk Inc. (Durham, NC)
- …Bachelor's degree in chemistry, biological sciences, or related field of study from an accredited university is required Minimum of eight years(8) years of experience in
- University of New Mexico - Hospitals (Rio Rancho, NM)
- …Coordinate all systems/services required for an organized, multidisciplinary, patient centered care team approach, and assure quality, cost-effective care for the
- Novo Nordisk Inc. (Durham, NC)
- …Bachelor's degree in Engineering or related field of study from an accredited university required Master's degree or industry equivalent experience preferred Minimum of
- Tris Pharma (Monmouth Junction, NJ)
- …compliance with all SOPs, cGMP, FDA, as well as all applicable company compliance guidelines, standards and objectivesOversee and manage the maintenance and tracking of
- Merck & Co. (Baton Rouge, LA)
- …and SCOPE The technician's job is to ensure the smooth running of the production system and to maintain equipment for which they are responsible in a specified
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Join a Legacy of Innovation 110 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …and lead the validation program for production equipment and processes used to support manufacturing of aseptic and terminally sterilized products. Lead the validation
- Merck & Co. (Irving, TX)
- …include providing technical support for Ruminant products and programs, including response to product inquiries and adverse reports in accordance with internal, FDA, CFIA