Generate, review, and approve all QA Labeling documentation with outstanding attention to detail.
Support QA labeling projects for new products, improvements, and labeling master document changes.
Review and approve lot-specific production labeling to ensure accuracy.
Populate, review, and approve IFU including lot-specific data when relevant.
Authorize IFU templates with revised lot-specific technical information.
Populate, review, and approve lot-specific technical data in technical/resource libraries.

🎯 Requirements

Bachelor’s Degree or equivalent experience in a relevant field.
2+ years in a regulated medical product environment.
Proficient in Microsoft Word, Excel, Adobe InDesign and/or NiceLabel Pro.

🎁 Benefits

Equal opportunities and a commitment to a diverse workforce.
Values: Passion, Curiosity, Integrity, Brilliance, Respect.

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