Product Labeling Specialist

Boston, MA

Responsibilities

 

  • Partake in the planning and implementation of the yearly marketing plan with a particular concentration on product labeling for both national and international markets.
  • Work closely with Regulatory to understand domestic and international product labeling and packaging requirements,
  • Work closely with the Marketing Product Managers, Product Development, and Project Management to understand the technical functionality of products so as to be able to translate them clearly and effectively into product labeling,
  • Manage multiple vendors, including technical writers, translation houses, packaging designers, creative designers and printers to develop product labeling, packaging, instructions for use and training materials for new products, and to revise labeling and/or packaging for existing products,
  • Ensure labeling changes are implemented in a consistent manner across different product lines for both the domestic and international markets.
  • Manage product labeling and packaging through the internal review process with Marketing, Regulatory, Engineering, and Manufacturing to ensure internal approval and smooth acceptance into finished goods.

 

Requirements

 

  • At least 3 years’ work experience in Product Labeling.
  • At least 3 years in the Quality function working with QSR and ISO 13485.
  • At least 1-year experience working with UDI/GTIN requirements
  • Healthcare/life sciences labeling experience required.
  • Must have ability to understand medical/clinical and technical aspects of product.
  • Medical device or pharmaceutical industry labeling experience required.
  • Vendor management experience required.
  • Demonstrate a solid working knowledge of FDA labeling.
  • Moderate to expert proficiency with Adobe Creative Cloud, including InDesign, Illustrator, and Photoshop
  • Ability to design on-demand product labeling in BarTender software preferred.
  • Experience developing artworks and graphics, and electronic publications, for regulated medical products
  • Experience with document management systems, such as Agile PLM and SharePoint
  • Knowledge with MS Office, including Outlook, Project, and Visio
  • Knowledge of labeling workflow from creation to obsolescence

 

 

 

 

Note: Qualified candidates will be contacted within 2 business days of application. If an applicant does not meet the above criteria, we will keep your resume on file for future opportunities and may contact you for further discussion.

Date Posted 1/28/2020
Salary $40.00/hr






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