Jobs · Massachusetts

Associate Director, Quality Technology Delivery

Alnylam Pharmaceuticals · Cambridge, MA · 3 days ago
$172k–$233k/yrFull-time

Key Responsibilities

  • Lead Delivery of Technology Systems Supporting QMS Processes
  • Manage implementation, enhancement, and integration of technology platforms that support QMS processes, including: Veeva Quality Suite (QMS, Docs, Training, etc.), LabWare Laboratory Information Management System (LIMS) for Quality and Quality Control (QC) lab environments, SAP S/4 Quality Management (QM) and related Quality modules
  • Ensure solutions are delivered on time, within scope, and aligned with business requirements
  • Drive issue resolution, risk management, and escalation as needed
  • Manage Technology Vendor Delivery and System Operations
  • Oversee day-to-day execution of vendor-delivered work across Quality systems
  • Ensure vendors meet agreed timelines, IT standards, and service levels
  • Coordinate across multiple vendors and internal teams to deliver integrated solutions
  • Partner with Quality to Enable Effective Solutions
  • Work closely with Quality stakeholders to understand business needs and translate them into IT system requirements
  • Ensure solutions align with Quality-owned business processes and workflows, and enable standardized, scalable ways of working
  • Support user readiness and enablement, with adoption led by Quality and other business stakeholders
  • Act as a trusted partner to Quality teams for system-related needs and improvements
  • Support Data Integration and Reporting (in partnership with IT Data & Artificial Intelligence)
  • Collaborate with IT Data & AI to ensure Quality data is captured, structured, and accessible for reporting and analytics
  • Enable consistent data flows across lab, manufacturing, and Quality domains
  • Help ensure data quality, consistency, and traceability across systems

Required Qualifications

  • B.S., M.S., or Ph.D. in a science or engineering discipline
  • 10+ years of experience supporting Quality IT systems in life sciences
  • Strong understanding of GxP, Quality processes, and regulatory requirements
  • Proven experience delivering enterprise systems (e.g., Veeva)
  • Experience managing system implementations and working with external vendors
  • Strong program and project management skills
  • Able to work effectively with business stakeholders and cross-functional teams
  • Experience operating in regulated environments with audit/inspection exposure

Preferred Qualifications

  • Experience with Veeva Quality Suite, LabWare LIMS, or SAP QM
  • Familiarity with system integration and data flows across enterprise applications
  • Experience supporting data and reporting use cases in Quality
  • Exposure to enterprise data platforms or analytics environments

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