Client: Medical Device Company
Location: Minneapolis- MN Onsite/Hybrid role (out of state Cn will have to have relocate to MN on their own)
Pay Rate- $45-50/hr W2
Contract Term: 12 months with possible extension.
NOTE: Visa transfers or sponsorship is not considered. This is not a C2C / 1099 role.
What products (if any) will this role support? This role will support labeling products (user guides, implant manuals, instructions for use) associated with medical devices across the Neuromodulation and Pelvic Health portfolios.
Top three required skills:
Job Description - Responsibilities may include the following and other duties may be assigned. · 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. · Understand and adhere to all quality management system documents and product commercialization procedures applicable to labeling development. · 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.
Responsibilities
Qualifications