Sr. Program Manager
$129,300–$258,700 year
On-sitePlymouth, Minnesota, United States
Job Summary
Lead cross-functional program management for moderately complex New Product Development (NPD) programs within the Structural Heart business. Identify process improvement opportunities, design and deploy PMO solutions for predictable execution, and formulate R&D policies to support profitable growth. Provide leadership to design and development teams through the transfer phase, manage departmental budgets, and guide documentation of test protocols and standard operating procedures. Interface with internal and external resources to ensure compliance with FDA regulations and Quality Management Systems, while contributing to business unit strategy planning and review boards.
Required Qualifications
- Bachelor's degree in a technical field, preferably mechanical, chemical, biomedical, industrial, or quality engineering; materials science, biochemistry, chemistry, physics or management
- Minimum of eight (8) years of experience in medical device development and/or other highly regulated industry
- Prior experience leading business process improvement and new product development
- Ability to work in a highly matrixed and geographically diverse business environment
- Ability to work within a team in a fast-paced, changing environment
- Ability to leverage and/or engage others to accomplish initiatives/projects
- Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization
- Multitasks, prioritizes and meets deadlines in timely manner
- Strong organizational and leadership skills, as well as attention to detail
- Ability to travel up to approximately 10%, including internationally
- Ability to maintain regular and predictable in-person attendance
Desired Qualifications
- Master's degree in a technical or business field
- PMP certification
- Prior people management experience
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