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!
...The primary duties of the Materials Coordinator will be to support all projects coming... ...higher education ~ Robust Medical and Dental plans with low-cost deductibles and premiums... ...Spending Accounts ~ Disability and Life insurance at no expense to you ~401(k) plan to...
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