MilfordFull TimeEngineering
Remotely
regulatory complianceindesigniso13485etqifunicelabel pro
Job Description
📋 Description
- 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.