Regulatory Affairs Talent in the Greater Philadelphia Region

20 years

MS

Experience in regulatory submissions, risk assessments, and consent decree. Industry: Pharmaceutical

20 years

BS

Experience in 510(k), IDE, PMA, CE marks, and global product registration. Industry: Medical Device

8 years

BS

Experience in new product registration, 510(k), EU, and CE mark. Industry: Medical Device

6 years

BS

Experience in global product registration, eCTD, and document management. Industry: Pharmaceutical, Medical Device

20 years

BS

Experience in submission management, CMC collaboration, labeling management, project management, and development of tracking tools. Industry: Pharmaceutical

12 years

BS

Experience in controlled document tracking, submission coordination, IND, annual reports, and PSURs. Industry: Pharmaceutical

6 years

BA

Experience in proofreading, labeling artwork, inserts, and Veeva Vault. Industry: Pharmaceutical

6 years

BA

Experience in labeling, promotional materials, ANDAs, amendments, and supplements. Industry: Pharmaceutical

4 years

PharmD

Experience in eMDR reporting, medical device submissions, and TrackWise. Industry: Medical Device