Position:
Senior Regulatory Affairs Specialist at Stryker Orthobiologics
Location:
Greater Philadelphia Area
Work:
Stryker Orthobiologics
- Malvern PA since Jun 2011
-
Senior Regulatory Affairs Specialist
Orthovita
Jul 2007 - Jun 2011
-
Senior Regulatory Affairs Specialist
Synthes
Mar 2006 - May 2007
-
Regulatory Affairs Specialist
Kensey Nash Corporation
Jul 1997 - Mar 2006
-
Regulatory Affairs Specialist
Skills:
Medical Devices, CE marking, ISO 13485, PMA, Design Control, FDA, Orthopedic, Biomaterials, 21 CFR, Medical Device Directive, ISO 14971, FDA GMP, Combination Products, Class III Medical Devices, Technical Files, Quality System, Surgical Instruments, Aseptic Processing, Spine, Biocompatibility, CAPA