Under minimal supervision, develops and maintains labels for medical devices. Collaborates with product subject matter experts to gather and assess labeling content. Executes label format and compiles content using specialized software. Audience for labels includes hospital and healthcare staff in global markets. Labels must comply with medical device regulations, standards, and business requirements.

**Essential Duties & Responsibilities**

+ Collaborate with product SMEs to assess and determine label requirements and content: Regulatory Affairs, Product Development, Product Safety Engineering, Packaging Engineers, Clinical Sciences, Marketing, Trade Compliance, etc.
+ Participate in new product label planning meetings and capture requirements using quality system planning documents.
+ Design label formats for functional usability by healthcare staff.
+ Use specialized labeling software to generate templates and enter label data, text, and graphics into label...