This position will be responsible for publishing electronic/paper regulatory submissions for US, European and rest of the world filings by working with Regulatory Affairs and project teams. If you possess 3 years of pharmaceutical/biotech industry experience with a minimum of 2 years of experience with publishing electronic/paper regulatory submissions.
Expert knowledge and experience with publishing eCTD submissions, and you're interested in working for an innovator in biotecnology, please contact me. Phone: +1 866-203-8227 x6606, or email:Sharon.Thornton@rightthinginc.com.
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