Engineering Program Manager
Full-timeMidR&DMedical DevicesUnknownBachelors
Description
The Engineering Program Manager plays a pivotal role in leading and supporting the cross-functional product development team. This position is central to guiding the planning and execution of development projects within a medical device development framework. The Engineering Program Manager is accountable for providing both strategic leadership and tactical execution across all project phases, ensuring the successful delivery of Company objectives that directly influence the advancement of innovative medical devices. An ideal candidate would leverage leadership, organization, and collaboration to help ensure success for a variety of strategic projects and initiatives, translating them into actionable roadmaps, setting priorities, and aligning resources. Tactically, the role involves hands-on management of daily project operations, troubleshooting project execution challenges, coordinating site activities, and ensuring milestones are achieved on-time and within scope. Examples include developing bottom’s up schedules, identifying critical path, and conducting detailed project reviews to drive accountability and communicate broadly across the organization. Responsibilities include leading cross-functional teams, developing and executing comprehensive project plans, acting as a central point of contact for project communication, monitoring project progress, facilitating meetings, providing updates to stakeholders, contributing to project management processes, and analyzing project timeline variances.
Requirements
Bachelor’s degree in engineering, life sciences, or a related technical field. Minimum of 5 years’ experience in medical device project management. Must be highly organized, skilled in planning, and proficient with project management tools and methodologies. Candidate must be highly collaborative, possess good interpersonal and presentation skills. Able to lead and motivate cross-functional teams to achieve critical corporate and project objectives. Must have working knowledge of ISO 13485 and 21 CFR 820. A demonstrated track record of medical device development and product commercialization processes (design control) success. The candidate must be a great team player; possess the ability to communicate clearly and effectively, both orally and in writing; oversee multiple tasks/projects, and the ability to think strategically while attending appropriately to details. Strong work ethic. PMP certification a plus.
Moximed
BIOTECHNOLOGY
Joint treatment
LocationCA - Fremont
Open Jobs8
Musculoskeletal
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