Project Manager for CE-IVDR and supply chain

AccuScan Sciences

$90K — $130K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree required; PMP certification preferred.
  • 3+ years of project or program management experience in biotech, diagnostics, or life sciences.
  • Experience with cross-functional milestone tracking and team coordination required.
  • Experience collaborating with laboratory operations, regulatory, and quality teams required.
  • Eligibility to work in the United States required.
  • Preferred experience in supporting CE-IVDR and regulated laboratory environments.
  • Preferred experience in clinical development programs related to oncology or molecular diagnostics.

Responsibilities

  • Maintain integrated project plans across cross-functional teams.
  • Monitor deliverables and dependencies aligned with product objectives.
  • Ensure adherence to development timelines; escalate risks as needed.
  • Facilitate cross-functional project meetings; track action items.
  • Manage timelines for CE-IVDR and the general supply chain.
  • Coordinate activities for inspection preparedness across functions.
  • Align laboratory operational readiness with accreditation and inspection timelines.
  • Proactively identify project risks and develop mitigation strategies.
  • Maintain clear communication among stakeholders.
  • Serve as the central point for project-level reporting.

Benefits

  • Comprehensive health insurance.
  • Retirement savings plan with company match.
  • Professional development opportunities.
  • Flexible work arrangements.
  • Supportive team culture focused on collaboration and innovation.
Full Job Description


As Project Manager, you will help drive cross-functional programs that support the development and operational readiness of complex diagnostic initiatives. This role plays an important part in keeping teams aligned around shared goals, maintaining momentum across interconnected workstreams, and supporting effective coordination among scientific, operational, regulatory, and quality-focused stakeholders.
Responsibilities
  • Maintain integrated project plans across cross-functional teams.
  • Monitor deliverables and dependencies aligned to product objectives.
  • Ensure adherence to development timelines and escalate risks as needed.
  • Facilitate cross-functional project meetings and track action items.
  • Manage the timeline for CE-IVDR and general supply chain.
  • Coordinate cross-functional activities required for inspection preparedness.
  • Align laboratory operational readiness with accreditation and inspection timelines.
  • Proactively identify project risks and mitigation strategies.
  • Maintain clear communication across stakeholders.
  • Serve as central point of coordination for project-level reporting.

Requirements
Qualifications
• Bachelor's degree required; PMP or equivalent certification is a plus.
• 3+ years of project or program management experience in biotech, diagnostics, or life sciences
• Experience with cross-functional milestone tracking and coordinating cross-functional teams required.
• Experience working with laboratory operations, regulatory, and quality teams required.
• Eligibility to work in the United States required.
• Experience supporting CE-IVDR, and regulated laboratory environments preferred.
• Experience supporting clinical development programs in oncology or molecular diagnostics preferred.

Benefits

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