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!
As a Medicial professional media, we are seeking for part-time or full-time medical English editors.Qualification & :1. Native English speakers with standard english pronunciation (British or American sound), and stable working availability.2. Having medical background...
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~ Maintenance Manager (Hands on)~ Industrial Products Manufacturer ~ Days, Monday - Friday ~$110,000 - $150,000~ North Chicago area About the Role My client, an industrial products manufacturer, is seeking a motivated Maintenance Manager with strong mechanical...