Sr. Mgr, Medical Device Safety: BS in Drug Regulatory Affairs, Nursing, Chem., Life Sci., Pharmacy or rel. + 6 yrs of exp. Use skills of medical device quality sys. regulations, global safety reporting regulations & guidelines, Pharmacovigilance Safety Database, case processing, medical device & combination product submissions, complaint handling & customer service in medical device or pharmaceutical industries, & clinical trials to serve as sr. SME on safety reporting requirements for medical devices & combination products. Bristol-Myers Squibb Company, Princeton, NJ. F/T. CV to resume.com@bms.com & ref. 4185. No calls/recruiters. No visa sponsorship.