“Regulatory: Smith & Nephew, Inc. (Cordova, TN) seeks Sr. Regulatory Affairs Specialist w/MS in engg., life sci., or reg. affairs +2 yrs. exp. with regulatory submission. Must have work experience with each of the following: 1. preparing domestic and global regulatory submissions (including 501(k), PMA, European dossier, Japanese STED and equivalent submissions for Australia and Canada); 2. clinical trial regulations; 3. developing and implementing improvements for regulatory submission process; 4. Electronic Labeling Requirements; and 5. supporting notified body audits. Apply online at www.smith-nephew.com No calls. EOE.”
Source: The Commercial Appeal. (2017, July 2). Localfieds. The Commercial Appeal, 176(183), p. 5C.