Click here to login or register
Reference # : 17-01108 Title : Labeling Specialist
Location : Jersey City, NJ
Position Type : Contract
Experience Level : Start Date / End Date : 09/04/2017 / 09/03/2018  

Project Description:

Under general supervision, responsible for the preparation of high-quality labeling documents for submission to the US Food and Drug Administration (FDA). Labeling documents include those prepared for FDA submissions, Annual Reports and PSURs in compliance with regulatory requirements and within company timelines.

Candidate will be required to work with limited oversight and have a basic understanding of FDA labeling regulations and FDA guidance's to the level of applying them effectively to all work output.
  • Assisting labeling managers with overall labeling process of brand prescription products.
  • Proofreading of package insert as well as packaging components.
  • Preparing redline documents and comparison charts.
  • Understanding of working in a digital workflow system and using online proofreading tools.
  • NDC number assignment.
  • Completion of electronic drug listing and conversion of label to structured product labeling (SPL).
  • Maintenance and posting of correct labels to company websites and Dailymed.
  • Maintain, catalog, and retain all labeling materials in accordance with company policies, procedures, and technologies.
  • Additional labeling / organizational responsibilities as needed.

Required Skills:
  • BA/BS required.
  • BA/BS with a Scientific or Regulatory background preferred.
  • 2+ years of pharmaceutical labeling experience; scientific background or familiarity with medical terminology.
  • Proficient in standard computer programs such as Microsoft Office, Excel, Word, Outlook, and SharePoint.
  • Excellent written communication and organizational skills
  • Works cooperatively with others; can also manage tasks and priorities independently as needed.
  • Takes responsibility for his/her own performance; promptly notifies his/her manager about any problems that affect his/her ability to accomplish planned goals.
  • Demonstrates flexibility in managing changing priorities and demands.
  • Food and Drug Administration (FDA) regulations and guidelines.
  • Current FDA/Regulatory Affairs submission requirements.
  • Logistics and work of the pharmaceutical industry.
  • Current Company policies, practices and procedures, including safety rules and regulations.

This 12+ month position starts ASAP.

Please E-MAIL your resume (attachment to email) with rate and availability to Karen: