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!
...Department: Dentist Location: Crestview, FL Compensation: $800 - $950 / day Description Req: 2510 A supportive team, patient-first mentality, and industry-leading benefits package are what you will enjoy as a member of our team. Are these missing in your...
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Responsible for the production management of the team according to production requirements.Arrange production tasks for each workstation based on the production tasks and operation plans assigned by the workshop director to ensure timely completion of production tasks....
...to grow your career globally across all divisions within DBG Health including Arrotex Pharmaceuticals, VidaCorp Consumer Goods, Independent Pharmacies of Australia Group, and Axe Health Services offer exciting prospects for advancing in their expanding markets...
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