Associate Director, CMC Technology Delivery
$172.2k - $233kAlnylam Pharmaceuticals
Overview:Alnylam is seeking an experienced leader to serve as Associate Director, CMC Technology Delivery to lead the digital enablement and transformation of end-to-end Chemistry, Manufacturing and Controls (CMC). This role will execute digital strategy, drive innovation, strengthen compliance, and enhance operational performance to help Alnylam CMC scale with agility and deliver business outcomes. The position reports to the Sr. Director, CMC, Manufacturing and Supply Chain Technology within the Research & Early Development (ReDev) and Technical Operations & Quality (TOQ) Technology organization.As a recognized subject matter expert, this leader will act as hands-on IT practitioner for the CMC organization enabling scalable, compliant, and efficient processes across starting material, drug substance and drug product process sciences, analytical sciences, CMC statistics and CMC program management from preclinical to clinical and commercial launch phase. This role will partner closely with the CMC business organization, IT software and service suppliers (e.g. Software-as-a-Service, system integrators), and internal IT teams-including Data/AI, Infrastructure Services, PMO to design, implement, and continuously improve CMC digital technology solutions across their full lifecycleHybrid role based in Cambridge, MA, with 3 days/week onsite.Responsibilities:Define and execute the IT solutions roadmap aligned with business priorities and digital transformation goals for CMC organizationsOversee the implementation and lifecycle management of digital CMC solutions that bring speed-to-market for new pipeline products from declaration of Development Candidate (DC) to regulatory filings for Investigational New Drug (IND) and New Drug Application (NDA) to commercial launchDrive implementation of digital and AI/ML capabilities that enable faster and efficient regulatory authoring, bring speed and reduce error rates through digital tech transfer of Drug Substance, Drug Product, analytical methods and data, and drive insights through access to data and analytical capabilitiesCollaborate with CMC and IT Data/AI teams to enable creation, transformation and storage of process recipe master and reference data, transactional data from lab runs, design of experiment (DOE) runs and batch execution runs, and derived data from processing of the results through statistical models and trending outputsDeploy digital capabilities that enable structuring and standardizing process recipe data for Critical Process Parameters, Critical Quality Attributes, In-Process Control parameters, Normal Operating Ranges, Proven Acceptable Ranges and allow recipe version management as the chemistry tech transfers from process development to process characterization through site characterization and Process Performance Qualifications (PPQs)Partner to develop data assets, AI/digital capabilities for CMC statistics for Process Development and Characterization, Process and Product Control strategy, implementing and supporting lifecycle management of trending toolsEnable digital capabilities that support CMC Program Management ranging from efficient transfer of programs from R&D to CMC, program start up and advancement enablement, program status reportingPartner with CMC, external Contract Manufacturing Organization (CMO), Software and Services partners, and Internal IT organization to develop data products, process templates, procedures and seamless system integrations (API/EDI) to enable efficient exchange of process dataProliferate user adoption of data, AI, digital and statistical analytics capabilities to accelerate use cases from research trending to Process Flow Descriptions (PFD) to regulatory specification filing, control strategy drafting, regulatory question responses to supporting commercial manufacturing for process control and monitoring, investigations and process optimizationPartner with the IT Data/AI team and the CMC organization to establish process data governance, process data stewardship, and process data products on the enterprise data platform to enable analytics and AI/ML capabilities for CMC operationsOwn end-to-end accountability for the lifecycle of CMC applications - from strategy and design through deployment, sustainment, upgrades, continuous improvement, and retirement. Partner with the business to define business case and articulate outcomes, manage total cost of ownership of digital solutionsEnsure systems meet GxP, data integrity, and global regulatory requirements (e.g. FDA 21 CFR), maintaining audit readinessDrive operational excellence by ensuring reliability, performance, compliance, and high-quality support of CMC systems (e.g., Empower, SoftMax Pro, Emerson Process Knowledge Management, QbDVision)Lead and mentor a team of cross-functional and IT resources. Oversee end-to-end delivery of initiatives and build strong partnerships with business stakeholders, IT teams, vendors, and procurementQualifications:Bachelor’s degree in Science, Engineering, Information Technology or related field10+ years of experience in CMC, Process Engineering or IT client-facing roles for CMC and Process/Analytical Development organizations in biopharmaceuticals or life sciences industryExperience with some of the following: regulatory filing process, understanding of recipe unit operations and data structures, statistical software and analytical trending tools (e.g. multi-variate data analysis, assay and control charts, JMP, Minitab, R, Python, SIMCA batch-on line, SEEQ, etc.)Exceptional stakeholder management and influencing skills with operations leaders and scientist user base. Change management and transformation leadershipExperience with data and systems integration, analytics, working with system integrators and managing IT suppliersExperience in regulated environments (GxP, computer systems validation, FDA 21 CFR regulations)Knowledge of full System Development Life Cycle (SDLC) - requirements, design, implementation, integration and testing, release and deployment, operations & maintenance, decommissioningDemonstrated success building and leading cross-functional teamsStrategic mindset with a pragmatic approach - balancing long-term vision with reliable delivery of measurable business outcomes10% travel maybe requiredPreferredMaster’s degree, MBA or PhDWorking knowledge of EDI, APIs, system integration and data transfersExperience with Agile & Scrum methodologies, leveraging Jira (or similar tools) for tracking projects risks, issues, tasks and user stories, and project management best practices.Familiarity with emerging AI, data and digital capabilities (data models, data lakehouse architecture, knowledge graphs, agentic AI, LLMs)About AlnylamWe 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.Before applying, please review Alnylam's Candidate Privacy Notice regarding how Alnylam handles Personal Data you provide with your application for employment.The pay range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus or sales incentive) and an annual long-term incentive award (e.g., equity).Alnylam’s robust Total Rewards package is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks. We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.Learn more about these and additional benefits offered by Alnylam by visiting the Benefits section of the Careers website: U.S. Pay Range$172,200—$233,000 USD
$143k - $233k
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$160.8k - $201k
...to Make a Difference Develops fit for purpose regulatory strategies incorporating totality of development (clinical, nonclinical, and CMC) and driving engagements that result in high value feedback from global health authorities and support Corporate objectives...Full time$172.2k - $233k
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...PK and oral bioavailability across species, formulations, and dose levels, and to support first-in-human dose selection.Partner with CMC to support formulation selection and optimization through PBBM.Develop IVIVC and mechanistic in vitro-in vivo dissolution models (e.g...$152.6k - $283.4k
...the RoleWe are seeking an accomplished Associate Director to join our discovery organization and... ...scientific strategy across ADC payloads, linker technologies, and conjugation approaches. This role... ..., translational sciences, and CMC teams to advance next-generation ADCsEvaluate...Full time- ## Associate Director, Regulatory Affairs CMCApplyremote type: Site Basedlocations: South Boston, MAtime type: Full timeposted on: Posted Todayjob... ...multiple novel therapies to patients. As the Regulatory CMC lead for these programs, you will have the opportunity to devise...Contract workRemote work
- Xenon Pharmaceuticals Inc. in Needham/Boston, MA, is seeking an Associate Director/Director of Development Program Management, CMC, to lead strategic and operational planning for CMC programs across early development. The role partners with CMC and program teams to translate...Remote job
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...Biogen seeks an Associate Director CMC Asset Lead to oversee end-to-end chemistry, manufacturing, and controls strategy for clinical immunology programs. This Pharmaceutical Operations & Technology role manages cross-functional teams, develops 5-year asset strategies,...$159k - $219k
...Molecules across various modalities. This Associate Director of Engineering position provides... ...team meetings, including engagement in CMC activities including authoring CMC section... ...development and execution of cutting-edge technologies in the service of delivering drug...Full timeContract workTemporary workLocal area$143k - $203k
...will be a key drug product SME for successful execution of the technology transfer of drug product processes to manufacturing site(s), providing... ..., review and ensure completion of drug product sections of CMC-regulatory submission documents (IND, IMPD, NDA, PIP, iPSP,...$169k - $204k
...of every strategic decision. Job DescriptionRole SummaryThe Associate Director of U.S. Trade & Distribution serves as the operational lead... ...monitoring Service Level Agreements (SLAs) for inventory stocking, delivery accuracy, and the Perfect Order Index (POI)Monitor trade-...Contract workTemporary workFlexible hours$164.02k - $221.91k
...patients while transforming your career.Associate Director, Commercial Drug Products & Life Cycle... ...Development organization, Drug Product Technologies unit that continuously strives to be a... ...manufacturing processes, high-quality CMC sections, and ensuring supply of commercial...Full timeTemporary workFlexible hours$145k - $240k
...supporting sourcing initiatives across multiple R&D functions, including areas such as Clinical, Translational Medicine, Research, and/or CMC.Demonstrated ability to partner effectively with internal stakeholders and deliver high-quality customer service in a fast-paced...Contract work$160k - $240k
...curiosity and inclusivity, so that our people are valued, seen, and heard.How you’ll make an impact:As the Associate Director, Analytical Development, you will contribute to CMC activities supporting mid and late phase clinical development of Kymera’s small-molecule protein...Contract work$154.4k - $242.55k
...About the role The Associate Director - Technology & Business Excellence Lead is responsible for providing technology and business leadership... ...biologics or small molecular programs with demonstrated delivery of new technologies such as PAT, high-throughput methods,...Minimum wageFull timeLocal areaWorldwide$152.6k - $283.4k
...Role We are seeking an accomplished Associate Director to join our discovery organization and... ...scientific strategy across ADC payloads, linker technologies, and conjugation approaches. This role... ..., translational sciences, and CMC teams to advance next-generation ADCs...$161.8k - $186.5k
...Reporting to the Vice President, Epic and Clinical Hospital Operations, the Director, Technology Portfolio Delivery and Strategic Initiatives, leads complex, high-visibility technology initiatives that support Dana-Farber’s transition into a new collaboration model and...Temporary workShift work$142.5k - $256.5k
...biotech industry.Reporting to the Director, Regulatory Information Management (RIM), the Associate Director, Regulatory Data... ...Affairs, Regulatory Operations, CMC, Labeling, Quality, Enterprise Data, Digital, and external technology partners to continuously improve...Permanent employmentFull timeFor contractorsWork at officeWork from home- ...Pharmaceuticals is seeking an Associate Director to lead laboratory... ...will partner with ReDev and CMC teams to translate business... ...ownership, and disciplined delivery in a regulated environment,... ...collaboration across IT, Quality Technology, #J-18808-Ljbffr Alnylam Pharmaceuticals
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