Program Manager II
$115,000–$150,000 year
On-site · Arden Hills, Minnesota, United States
Job Summary
Lead and manage multiple medical device development programs from concept through commercialization in a matrix organization. Own program plans, schedule adherence, budgets, scope changes, risk and issue management, and customer interactions; coordinate cross-functional teams across Development, Manufacturing, Supply Chain, Quality, and Regulatory Affairs; identify opportunities to add value beyond defined scope and optimize design-to-cost objectives. Requires strong communication skills, stakeholder management, and familiarity with FDA and ISO quality systems. Spanish-language ability is a plus.
Required Qualifications
- B.S. or M.S. in a technical field; PMP certification a plus
- 5-10 years experience in a customer-facing product development role
- Knowledge of electronics-based medical device technology; development cycles for software, mechanical and electrical disciplines
- Proficiency with MS Project; ability to develop schedules and budgets
- Excellent verbal and written communications; ability to convey technical concepts to diverse audiences
- Understanding of FDA, ISO 9001 and ISO 13485; experience across product development stages; capability to coordinate multi-disciplinary teams
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