Alnylam Pharmaceuticals logo

Executive Director, Quality Technology & Analytics

Alnylam Pharmaceuticals
Full-time
Remote friendly (Cambridge, MA)
Worldwide
IT
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Overview:

The Executive Director, Quality Technology & Analytics, is responsible for driving the Quality technology strategy and innovations across Alnylam enterprise capabilities globally. This individual owns the strategy and is the technical leader to oversee the governance of systems owned by Quality (e.g., Veeva Vault, DocuSign, Insights, the Analytics Dashboards, and the Quality Dashboard), and is accountable to ensure not only compliance but to drive innovative solutions within Quality and in service of our business partners. This individual will provide oversight and strategic leadership in all matters that relate to GXP systems, such as configuration management, integrations, data quality, data management, data retention, etc. They are accountable for policy implementation that ensures regulatory compliance and appropriate controls, to include data governance and stewardship. This role is critical to ensure the effective implementation, maintenance, and overall state of data quality to support global, enterprise operations.


Responsibilities:

Driving Quality Technology Strategy:

  • Define and drive the Quality Technology & Analytics roadmap, aligned across GxP enterprise functions including research, development, manufacturing, supply chain and commercial.
  • Provide oversight and governance to ensure enterprise systems in a state of ongoing compliance and inspection readiness while driving the successful innovation and evolution of key systems such as Veeva, ERP, LIMS, etc.
  • Responsible to interpret and translate business needs into scalable, system-agnostic reporting tools in close partnership with Quality Systems and enterprise data teams.
  • Evaluate and provide innovative solutions that optimize existing capabilities.

Ensuring Regulatory Excellence and Compliance:

  • Responsible to ensure policy, process and governance is in place to ensure compliance is maintained for GxP computerized system validation (CSV).
  • Ensure controls are in place and monitored across the enterprise, such as routine audits and periodic system reviews that ensure compliance with FDA, EMA, and other regulatory bodies.
  • Responsible to ensure the team develops validation strategies using fit-for-purpose, risk-based methodologies and pragmatic approaches.
  • Responsible to ensure technology compliance investigations for GxP systems are performed by technically qualified individuals and in collaboration with IT and relevant business partners. This role may personally support incidence response to potential cyber-security attacks threatening the enterprise.

Driving Digital Transformation:

  • Develop the strategy and drive efforts to modernize legacy systems and transition to cloud-native platforms.
  • Enable advanced analytics, machine learning, and AI-driven decision-making in collaboration with Quality, IT, and Business Ops.
  • Ensure resource and capabilities are in place to drive the adoption of automation and data analytics across GxP critical functions (manufacturing, research, development, supply chain and commercial).

Enabling Data-Driven Quality:

  • Implement robust data governance, collection, and master data management practices.
  • Define and implement data standards for cross-system reporting and integration across the enterprise.
  • Define and drive best practices for data integrity across GxP stakeholders
  • Collaborate with Data Privacy to ensure electronic solutions are compliant with global standards.

Leading Cross-Functional Collaboration:

  • Partner GxP Quality Functions, Regulatory Affairs, IT, and various business stakeholders to align tech with business outcomes and regulatory expectations.
  • Act as a bridge between IT and Quality, relevant business operations to enable real-time data flow and system integration.

Team & Vendor Leadership:

  • Build and lead cross-functional teams across IT, research, development, manufacturing, supply chain and commercial.
  • Foster a culture of learning, agility, and collaboration.
  • Optimize costs while scaling innovation and owning the quality technology budget.


Competencies:

  • Deep knowledge of GxP, HIPAA, FDA, EMA, MHRA compliance, and clinical informatics.
  • Experience with quality management processes (Document Management/Control, Learning Management System, Quality Event/CAPA, Audit & Inspection Management).
  • Deep understanding of global regulations and guidelines for electronic quality systems, data integrity, electronic records, and electronic signatures including 21 CFR Part 11, Annex 11 and ALCOA++ principles of data integrity.
  • Demonstrated expertise in system configuration, Software Life Cycle (SLC) Software Development Life Cycle (SDLC) validation and compliance.
  • Strategic mindset with execution-focus and passion for innovation.
  • Effective oral and written communication skills.
  • Excellent organizational and analytical skills and demonstrated ability to handle multiple projects at the same time and shift priorities when needed to meet a constantly changing environment.
  • Ability to demonstrate clear alignment with Alnylam Core Values at a leadership level.


Qualifications:

  • 15-20+ years of experience in technology leadership, preferably in life sciences, biotech, or pharmaceuticals.
  • Bachelor of Arts, Bachelor of Science, or equivalent work experience
  • 5+ years of experience with Veeva Vault Quality or similar quality management systems.
  • 5+ years of experience leading and developing teams
  • Strong understanding of GxP, HIPAA, FDA, EMA, MHRA compliance and clinical informatics.
  • Demonstrated experience in system configuration, validation, and compliance management
  • Demonstrated experience leading cross-functional initiatives
  • Experience with quality management processes and systems (e.g., document control, training management, change control, CAPA)
  • Strategic mindset paired with a can-do attitude.
  • Passion for technology and innovation


About Alnylam: We are the leader in RNAi therapeutics – a revolutionary approach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possible and are just at the beginning of what’s possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people. We're proud to be a globally recognized top employer, where an authentic, inclusive culture and breakthrough thinking fuel one another.


At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to their sex, gender or gender identity, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law. Alnylam is an E-Verify Employer.