Lead product systems development efforts for multiple projects and initiatives across the full range of FDA Class II regulated product development, from early front-end innovation through development, commercialization, and post-market surveillance. Learn and execute product development processes, including design controls, risk management, specification management, and process validation. Guide cross-functional quality, engineering, research, and manufacturing team members through design control processes. Develop product milestones, budgets, timelines, and resource forecasts for assigned projects, and ensure that product specifications and quality plans are appropriate for each project phase. Facilitate discussions with marketing and design teams regarding claims and aesthetics, and mentor junior product development team members. Plan and carry out project responsibilities with limited assistance and direction; identify and solve problems, determine root causes of complex technical issues, and recommend solutions. Build mastery of medical device product development principles and test methods and apply them to development projects. The role is based at the Neenah - West R&E Office and uses a flexible work model that blends remote work with intentional in-person collaboration. Travel of up to 15% domestically and internationally may be required. The position is full-time and regular. The salary range is $87,260–$107,780 USD, with eligibility for a target bonus and a benefits package that includes a 401(k) and Profit Sharing plan. Kimberly-Clark does not provide relocation support for this role, but may provide immigration visa and work authorization assistance and financial support to the selected candidate if needed.
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Job Type
Full-time
Career Level
Senior