Associate Director, Strategic Program Management

Added
17 minutes ago
Type
Full time
Salary
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Related skills

program management regulatory affairs validation biotechnology design controls

๐Ÿ“‹ Description

  • Lead complex IVD/CDx programs through development, design transfer, validation, and PMA submission
  • Build and maintain an integrated program plan covering deliverables, resources, dependencies
  • Partner with functional leaders to define objectives, development priorities, success criteria, and
  • Anticipate risks, identify gaps and trade-offs, and drive timely decisions across functions
  • Establish clear program governance, ownership, escalation paths, and accountability for commitments
  • Integrate assay development, design controls, software and bioinformatics, analytical validation

๐ŸŽฏ Requirements

  • Bachelor's degree in life sciences, engineering, or a related field, or equivalent relevant
  • 10+ years of progressive program or project management experience in molecular diagnostics, in
  • Direct experience leading CDx or IVD development programs involving design controls, validation
  • Experience building and driving integrated plans across technical, clinical, regulatory, quality
  • Demonstrated ability to lead senior cross-functional stakeholders, resolve competing priorities
  • Experience presenting complex programs, risks, and recommendations to executive leadership

๐ŸŽ Benefits

  • Comprehensive medical, dental, vision, life and disability plans for eligible employees and their
  • Free testing for Natera employees and their immediate families
  • Fertility care benefits
  • Pregnancy and baby bonding leave
  • 401k benefits
  • Commuter benefits
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