Labeling Specialist
Redbock - an NES Fircroft company, Minneapolis, Minnesota, United States, 55400
Labeling Specifications Specialist (24 month contract // Minneapolis, MN):
Duties:
Creates, reviews, and reproduces text required for labeling medical products.
Ensures that labeling, art, film, and plate proofs meet all medical, legal, and regulatory requirements.
Monitors changes in labeling regulations in the US and/or abroad.
Reviews promotional and commercial communication material and ensures that it is supported by the data and consistent with the application.
Monitor, evaluate and recommend improvements to labeling processes, quality, systems tools and/or policies.
1 years of experience required
Basic understanding of package label requirements for medical device
Experience with PLM systems for routing design documentation (Enovia, Agile, Windchill)
Interact with internal marketing, R&D, QA, and project managers to provide regulatory input and guidance on changes to currently marketed products and for new product development.
Previous experience with the development of package labeling designs
Working knowledge of the Microsoft Office suite
Skills with Adobe CS3 (or later) publishing suite of software, including InDesign, Illustrator and Photoshop
High degree of accuracy and strong proofing skills
Problem-solving, organization, and prioritization skills
Preferred Requirements:
Experience in the development of labeling for the medical device industry preferred.
Bachelor's Degree in Graphic Arts or Packaging Engineering background preferred
Ability to use computers and other graphic-arts related technology
Ability to understand the Engineering Change Request (ECR) process using a document control system
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Creates, reviews, and reproduces text required for labeling medical products.
Ensures that labeling, art, film, and plate proofs meet all medical, legal, and regulatory requirements.
Monitors changes in labeling regulations in the US and/or abroad.
Reviews promotional and commercial communication material and ensures that it is supported by the data and consistent with the application.
Monitor, evaluate and recommend improvements to labeling processes, quality, systems tools and/or policies.
1 years of experience required
Basic understanding of package label requirements for medical device
Experience with PLM systems for routing design documentation (Enovia, Agile, Windchill)
Interact with internal marketing, R&D, QA, and project managers to provide regulatory input and guidance on changes to currently marketed products and for new product development.
Previous experience with the development of package labeling designs
Working knowledge of the Microsoft Office suite
Skills with Adobe CS3 (or later) publishing suite of software, including InDesign, Illustrator and Photoshop
High degree of accuracy and strong proofing skills
Problem-solving, organization, and prioritization skills
Preferred Requirements:
Experience in the development of labeling for the medical device industry preferred.
Bachelor's Degree in Graphic Arts or Packaging Engineering background preferred
Ability to use computers and other graphic-arts related technology
Ability to understand the Engineering Change Request (ECR) process using a document control system
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