Technical Writer

• Plan, research, develop, and write medical device labeling, and manage labeling deliverables as part of cross-functional project teams under general supervision
• Simultaneously manage up to two labeling updates and one small, new-product-introduction project that involves multiple labeling pieces
• Conducts interviews with various users and technical staff to gather data for documentation
• Recommends formats responsive to technical and customer requirements
• Assist in providing documentation for CAPAs, and departmental and business-unit audits
• Contribute to time and cost estimates for labeling deliverables for project teams
• Develop illustrations in cooperation with professional illustrators
• Participate on department and business-unit initiatives
• Oversee Engineering Change Order process for labeling
• Coordinate translations and track the status of translations
• Complete labeling proofs, develop documentation for regulatory submissions, and carry out other tasks as assigned.

Senior Technical Writer

Technical Writer

Scientist – GMP Quality, Technical Writing