Careers
We are always looking for self-driven and motivated personnel at all levels in pharmaceutical manufacturing, analytical laboratory, materials management and administrative staff. We are proud to offer employment opportunities to professionals looking to make the step up with an ambitious, results-oriented company.
|
|
DIRECTOR, REGULATORY AFFAIRS (full time) in Amityville, NY: Evaluate regulations, design & implement registration strategies, prepare compile & submit high-quality original regulatory submissions, monitor labeling activities, review post-mktg reports, interact with responsible departments and lead preparation, critical review of regulatory applications & assemble scientific (nonclinical, clinical, & manufacturing) & administrative sections of submissions, review & develop company practices and policies, exercise sound management & clinical jdgmt in making appropriate decisions, and act independently. Min. qualifications: BS in Pharmacy, Chemistry, Pharmaceutical Chemistry or related plus minimum 5 yrs exp. with pharmaceutical regulatory affairs & regulatory submissions. Skills in eCTD, ANDA (21 CFR 314), labeling, regulatory strategy, SUPAC, post marketing reports, ICH & FDA, CMC documentation & pharmaceutical product devpt. Send resumes to INNOGENIX INC 8200 New Horizons Blvd, Amityville, NY 11701 or email to careers@innogenix.com. Ref job id REG002
|