#5357209
20 years
MS
Experience in regulatory submissions, risk assessments, and consent decree. Industry: Pharmaceutical
#339799
20 years
BS
Experience in 510(k), IDE, PMA, CE marks, and global product registration. Industry: Medical Device
#1565689
8 years
BS
Experience in new product registration, 510(k), EU, and CE mark. Industry: Medical Device
#5357215
6 years
BS
Experience in global product registration, eCTD, and document management. Industry: Pharmaceutical, Medical Device
#2267428
20 years
BS
Experience in submission management, CMC collaboration, labeling management, project management, and development of tracking tools. Industry: Pharmaceutical
#1285843
12 years
BS
Experience in controlled document tracking, submission coordination, IND, annual reports, and PSURs. Industry: Pharmaceutical
#5331909
6 years
BA
Experience in proofreading, labeling artwork, inserts, and Veeva Vault. Industry: Pharmaceutical
#2855525
6 years
BA
Experience in labeling, promotional materials, ANDAs, amendments, and supplements. Industry: Pharmaceutical
#1509457
4 years
PharmD
Experience in eMDR reporting, medical device submissions, and TrackWise. Industry: Medical Device
Job Title: Regulatory Affairs Consultant
City: Philadelphia
Candidate(s):