Documentation Specialist II – Regulatory Specialist (19-00883) – NJ – Bridgewater


  • Review the Master Product List and ensure all marketed products are drug listed (posted on DailyMed)
  • Drug Listing Activities: Drug Listing of new products
  • DEA and state registration renewals for PSE; create work instructions for DEA and each State
  • Processing of payments for Export Certificate Program invoices
  • Assist in the preparation of Alcohol and Tobacco Tax and Trade Bureau (TTB) Reports
  • Processing of invoices from vendors and consultants
  • Put through the approval process revised or newly created SOPs, as applicable
  • SHARE updates to support enhancement initiatives for the migration of data to Veeva Vault system
  • Special projects as assigned

Proficient in Microsoft Office, Internet Savvy and Adaptable to New Systems & Programs, Communication Skills, Organization & Project Coordination Skills

Bachelor's Degree (preferred) or equivalent experience
Source: Job Diva – Job Listing

Leave a Reply

Your email address will not be published. Required fields are marked *