Sr. Program Manager - Project & Portfolio Management Office (assay Development, Ivd)

Danaher

Sunnyvale, CA, US
Base: $150,000-$170,000; bonus/equity: eligible fo...
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5+ years product development experience
Molecular diagnostics background
Medical device industry experience
** Danaher is seeking a Senior Program Manager for its Program Management Office at Cepheid in Sunnyvale, CA. The role focuses on leading new product development projects in the molecular diagnostics sector, ensuring timely and budget-compliant delivery while fostering a culture of continuous improvement. **

Job Summary

  • The Senior Program Manager leads New Product Development and Market Expansion projects in a molecular in-vitro diagnostic context to deliver on time and within budget.
  • This role requires establishing tracking, reporting, and resource capacity planning to enable timely decisions and keep teams aligned to milestones.
  • Cepheid offers comprehensive benefit programs including paid time off, medical/dental/vision insurance, and 401(k) to eligible employees.

Matching Summary

Match Score: 75

** Danaher is seeking a Senior Program Manager for its Program Management Office at Cepheid in Sunnyvale, CA. The role focuses on leading new product development projects in the molecular diagnostics sector, ensuring timely and budget-compliant delivery while fostering a culture of continuous improvement. **

Salary

Base: $150,000-$170,000; Bonus/Equity: Eligible for bonus/incentive pay; Benefits: Comprehensive package including PTO, medical/dental/vision, 401(k)

Skills & Requirements

Must-have

  • 5+ years product development experience
  • Molecular Diagnostics background
  • Medical device industry experience
  • Regulated environment knowledge
  • US-IVD and CE-IVDR compliance

Nice-to-have

  • Danaher Business System expertise
  • PMP Certification preferred
  • VPM or PSP certification status
  • Continuous improvement culture
  • Global strategy translation skills

Key Requirements

  • Bachelor's degree required, Master's preferred
  • Minimum five years leading product development
  • Experience in regulated medical device industry
  • Track record of commercialization success

Work Rights

Not specified

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