Role Overview
ASP is looking for a Senior Program Manager who thrives on complexity and impact. In this role, reporting to the PMO Director, you will be accountable for leading multiple cross-functional teams and driving execution across high-visibility, complex programs with minimal oversight.
What You Will Do
Lead Complex Medical Device Programs: Lead high-impact medical device development programs across hardware, systems, and consumables from concept through commercialization, ensuring delivery against business, customer, and regulatory expectations.
Why It Might Be a Fit
Exceptional program and project management skills, with a proven ability to lead cross-functional teams through complex, high-impact initiatives. Agile leadership with familiarity with SAFe, and Lean practices.
Requirements
- 6+ years of program management experience leading end-to-end product development and commercialization of regulated products.
- 4+ years in the Medical Device industry, including hands-on experience leading programs that resulted in FDA 510(k) clearance, with working knowledge of 21 CFR 820 and ISO 13485.
- Bachelor's degree in Engineering, Life Sciences, or a related technical discipline required.
- Certification preferred: PMP, PgMP, or equivalent.
Benefits
- Domestic and international travel
- Scheduled work hours
- Remote work option
- Health and safety training
- Ergonomic risk assessment
- Reproductive health risk assessment
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