Featured Job
-
Job Removed or Not Found
Related Jobs
- Novo Nordisk Inc. (Plainsboro, NJ)
- …A Bachelor's degree and a minimum of twelve (12) years pharmaceutical, legal, regulatory, or compliance experience OR an advanced degree with a minimum of 10 years
- Novo Nordisk Inc. (Boulder, CO)
- …Bachelor's degree in Science, Business, or related discipline with five (5) years of experience in pharmaceutical or related industry required Master's degree with three
- Daiichi Sankyo, Inc. (Bernards, NJ)
- Join a Legacy of Innovation 125 Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve
- Eisai, Inc (Raleigh, NC)
- …include ensuring an uninterrupted supply of quality products and successful and timely launch of new products.As the manufacturing network and global supply chain become
- Eisai, Inc (Exton, PA)
- …(IQ), Operating Qualifications (OQ), Production Qualifications (PQ) and IT regulation (eg 21 CFR Part 11, Data Integrity) compliance as assigned.Collaborates with project
- Merck & Co. (Rahway, NJ)
- …Employee/Retiree Support: Support transitioning employees at all levels in their understanding of key compensation and benefits programs at critical moments in their
- Merck & Co. (Knoxville, TN)
- …& Activities include and may not be limited to: Engaging in balanced product sales presentations with Health Care Providers and Health Care Business Professionals to
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Recruits, hires, trains, retains, develops and leads diverse, high performing representatives to their full potential. Conducts field travel with each District
- Genmab (NJ)
- …experience, and location. Also, certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives. When you join
- Merck & Co. (Rahway, NJ)
- …The Senior Statistical Programmer, Submission Data Standards Quality Management (SDS QM), provides oversight and quality management of submission data standard
