One of our large Medical Device clients is looking for a quality proofreader to join their team for various projects. This person is responsible for ensuring high-quality documentation and compliance within the label design and development process to verify that all labeling meets regulatory and design requirements. The role includes accountability for the quality review of labeling for New Product Development, Lifecycle Management, and Process Improvement projects for Worldwide Product Labeling (WWPL) within a franchise of Global Surgery. Key responsibilities include: following established procedures to perform quality reviews and edits of product labeling and packaging graphics, documenting the quality review results as per Good Documentation Practices and providing constructive feedback for iterative design improvements by graphic designers. They will also be responsible for conducting thorough reviews for compliance with content, format, grammar, punctuation, electronic navigation (hyperlinking), spelling, symbology, and regulatory standards, and approving final documentation, blue-lines, or color proofs supplied by vendors as necessary as well as verifying design templates to ensure consistency in standardized label/IFU work. This is a hybrid role and is starting as a 12 month contract.
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-3+ years proofreading within a medical device or pharmaceutical company
-Experience with Adaptiv
-Quality background reviewing and approving quality documents
-Experience in Medical Devices/Labeling
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.