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Alnylam Pharmaceuticals

Associate Director, CMC Technology Delivery

cambridge, MA

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About this opportunity

Alnylam Pharmaceuticals lists this Associate Director, CMC Technology Delivery opportunity in cambridge, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.

Job description

Responsibilities:

Define and execute the IT solutions roadmap for CMC digital transformation.

Oversee implementation and lifecycle management of digital CMC solutions to speed new pipeline products from Development Candidate through IND/NDA filings to commercial launch.

Deliver digital and AI/ML capabilities for faster regulatory authoring and reduced error rates via digital tech transfer of Drug Substance/Drug Product/analytical methods and data.

Enable creation, transformation, and storage of recipe master/reference data, transactional lab run data, DOE/batch execution data, and derived statistical/trending outputs.

Standardize/structure process recipe data (CPPs/CCAs/In-Process Controls/operating ranges) with recipe version management.

Develop CMC statistics assets and trending tools; enable CMC program management digitization and reporting.

Create data products, templates, procedures, and seamless integrations (API/EDI) for process data exchange.

Establish process data governance/stewardship and publish data products to support analytics/AI/ML.

Own end-to-end lifecycle of CMC applications (strategy/design through deployment, sustainment, upgrades, continuous improvement, retirement); define business cases and manage TCO.

Ensure GxP/data integrity/global regulatory compliance and audit readiness.

Drive operational excellence for CMC systems (e.g., Empower, SoftMax Pro, Emerson Process Knowledge Management, QbDVision).

Lead and mentor cross-functional delivery; partner with stakeholders, IT, vendors, and procurement.

Qualifications:

Required: Bachelor’s degree in Science/Engineering/IT or related field.

10+ years in CMC, Process Engineering, or IT client-facing roles in biopharma/life sciences.

Knowledge of regulatory filing, recipe unit operations/data structures; statistical software/trending tools (e.g., JMP, Minitab, R/Python, SIMCA, SEEQ).

Strong stakeholder management/change leadership.

Data and systems integration experience with IT suppliers/integrators.

Regulated environment experience (GxP, computer systems validation, FDA 21 CFR).

SDLC knowledge (requirements through decommissioning).

Proven cross-functional team leadership; strategic + pragmatic delivery.

Up to ~10% travel.

Preferred: Master’s/MBA/PhD.

Working knowledge of EDI/APIs/data transfers and system integration.

Agile/Scrum and Jira (or similar) experience.

Familiarity with AI/data/digital capabilities (data models, lakehouse, knowledge graphs, agentic AI, LLMs).

Benefits (explicitly stated):

Medical/dental/vision, life/disability insurance, lifestyle reimbursement, flexible spending/HSAs, 401(k) match, paid time off, wellness days, holidays, and recharge breaks.

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Worksite address

cambridge, MA, 02140, US

Who can apply

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