Overview This is a contract position within the Instruction Design/Human Factors Engineering group, working 40 hrs/week for 1 year, with potential renewal. Responsibilities Review new and updated Instructions for Use (IFUs), reference guides, and carton artwork content and graphics for medical device/combination products to ensure accuracy. Some reviews use digital comparison tools; others require manual checking. Maintain change history of instruction materials during development, including changes from regulatory authorities and Human Factors studies. Ensure changes to specific projects are communicated to other programs for implementation. Support extension of department platform designs into individual projects; communicate daily with other designers on impact to platform designs, and update platforms as appropriate. Develop instruction design strategies for individual projects that align with department and corporate instruction platforms; coordinate with cross-functional teams (Human Factors, Device Engineering, Marketing Labeling, Clinical, Legal and Regulatory Affairs) to define instructional requirements and execute plans. Support process improvement programs and documentation related to design and development processes. Top 6 Must-Have Skill Sets Minimum 4-6 years of experience reviewing documents including medical device IFUs, with strong proficiency in rapid sketch illustration, digital line-art illustration, and image editing. 2-4 years experience using Adobe Creative Suite software (InDesign and Illustrator) and Microsoft Word and Excel; knowledge of Microsoft Access and Visio is a plus. High level of attention to detail and accuracy in reducing errors in deliverables. Background in medical, healthcare, medical devices and/or pharmaceuticals. Strong punctuality, reliability, flexibility, and ability to balance multiple detail-oriented projects; strong organization and communication skills. Collaborative mindset; ability to work with cross-functional teams. Basic Qualifications Bachelor’s degree and 2 years of experience Associate’s degree and 6 years of experience High school diploma / GED and 8 years of experience Seniority level Mid-Senior level Employment type Contract Job function Instruction Design / Human Factors Engineering Industries Pharmaceutical Manufacturing #J-18808-Ljbffr ACL Digital
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