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Technical Writer- CMC Company Name: Biobridges, LLC PROJECT DETAILS: Write and/or review CMC sections of regulatory submissions (NDA, MAA, IND, Annual Reports) using CTD and eCTD format. Help prepare submissions for regulatory filings. Support, as needed, any additional regulatory or quality related writing projects. REQUIREMENTS: BS/BA degree, preferably in the pharmaceutical industry or related scientific field. At least 4 years of experience in writing pharmaceutical development reports, regulatory writing or. After registering you may be able to apply for this job directly (if still active) on ((None))'s site. Future job matches may be sent from Geebo approved job partners.
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