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Senior Program Manager
| Company | Sibel Health |
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| Location | Chicago, IL, USA |
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| Salary | $130000 – $165000 |
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| Type | Full-Time |
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| Degrees | Bachelor’s |
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| Experience Level | Senior |
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Requirements
- 5+ years of experience in Program Management in New Product Development/Introduction
- Bachelor’s Degree in Computer Science, Engineering, or related field
- 5+ years in medical device product development, or other highly regulated environment (Ex. Automotive, Military)
- Excellent leadership and communication skills
- Demonstrated track record of successfully leading programs to completion
- Excellent knowledge of core functional areas for hardware development
- Highly developed skill set in program leadership practice
- Good balance of high-level strategic and detailed tactical thought processes
- Possess managerial courage
- Independent, self-directed, and highly self-aware
- Familiarity with G-suite, Jira, Slack, Smartsheet, and other program management tools
Responsibilities
- Own program planning, execution, and delivery, in support of Sibel Health’s business goals
- Ensure all essential foundational elements of program management are created, maintained, and reported on
- Lead the team in adherence to organizational tools, processes, and requirements throughout the development lifecycle
- Support the team in removing roadblocks during program execution
- Facilitate day-to-day communication and activities of the Core Team
- Manage risks proactively, preparing mitigation plans as a team
- Escalate issues, barriers, or concerns as appropriate to relevant stakeholders or leadership
- Support PMO in identifying improvements to existing, and/or development of new, program management processes, systems and tools
- Up to 10% international travel required
Preferred Qualifications
- 8+ years of experience leading new product development/introduction programs in the medical device industry
- Thorough understanding of core program management principles
- Experience leading programs and program deliverables with international teams and external contract services
- PMP (Project Management Professional), Certified Scrum Master, PRINCE2 certification
- Exceptional influencing and interpersonal skills
- Successfully managed multiple programs from conception through commercialization ideally in the medical device industry
- Exposure to systems engineering, concept engineering, hardware and software development, validation and systems integration
- Experience in FDA regulatory submission (US) and/or CE mark regulatory submissions (EU)
- Experience in regulatory submissions requiring clinical studies (510k clinicals and/or IDE/PMA clinicals)
