Demo

Labeling Specialist

Integrated Resources, Inc ( IRI )
Millsboro, DE Full Time
POSTED ON 2/9/2025
AVAILABLE BEFORE 5/3/2025

Hybrid schedule (require to be onsite for 3 days / week -Tuesday and Wednesday fixed) 3rd day can be discussed when on assignment.

Responsibilities :

This position is responsible but is not limited to the following duties :

  • Prepare new / revised label packaging for regulatory submissions to the USDA and maintain regulatory documents to ensure site compliance.
  • Support regulatory filing submissions with the USDA for both domestic and international product packaging.
  • Independently work with internal stakeholders, regulated packaging processes and system workflows to revise or draft new packaging for vaccine biologicals for both US (domestic) and international markets.
  • Ensure prompt availability of labels and artworks and liaises with departments such as Marketing, Pharmacovigilance and Technical Services to ensure compliance with established regulations.

Required Experience and Skills :

  • With Associate, minimum 5-7 years of relevant experience within pharmaceutical labeling experience.
  • With Bachelor's, minimum 4-6 years of relevant experience within pharmaceutical labeling experience.
  • With Master's minimum 2-5 year of relevant experience within pharmaceutical labeling experience.
  • Require someone with scientific background or familiarity with medical terminology.
  • Require someone with excellent proofreading skills.
  • Proficient in standard computer programs such as Microsoft Office, Excel, Word, Outlook, SharePoint, ADOBE.
  • Preferred / nice to have :

  • Industry - Pharmaceutical Industry / Vaccine manufacturing / Medical and Biotechnology
  • Must have :

  • Regulatory labeling content review as per FDA guideline.
  • Quality check of labeling content errors.
  • Label artwork, label design review.
  • Support the preparation of labeling documents, coordinating labeling document submissions to regulatory bodies.
  • Looking for someone with labeling expertise in the pharmaceutical industry, vaccines manufacturing or GMP.
  • Typical day :

  • Very intensive label-oriented job
  • Need someone to hit the ground running.
  • Label review and submission of labeling documents and artwork
  • Label artwork, label design review.
  • Quality check for label content and formatting as per FDA guidelines.
  • Support the team with the review, revising labeling.
  • Attention to details.
  • Will prepare the label content following SOP's and FDA regulations.
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