Fidelis BioPharm

Morton Grove, IL, 60053, USA

  Manager, Regulatory Affairs   This individual will obtain and maintain regulatory approvals through paper and electronic submissions, assemble and submit new ANDAs, supplements, annual reports and amendments in a timely manner. They will also provide change control and validation plant support.             Advanced degree in a scientific/technical discipline with at least five to seven years of pharmaceutical industry experience.   Project management and/or supervisory experience required.   If you are interested in this position, please contact Eddie at ecotter@fidelisbiopharm.com .                                            

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