Intellia Therapeutics, Inc.

Manager CMC Program Operations

Intellia Therapeutics, Inc.$141K — $173K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s degree in a relevant field; PMP certification preferred
  • 6+ years in biopharmaceutical/life sciences, including CMC development
  • 2+ years dedicated to CMC or operations project management
  • Experienced in deploying AI-enabled or automated tools
  • Strong project management skills with risk management experience

Responsibilities

  • Build and maintain a master CMC project plan to identify task interdependencies and monitor schedule risks
  • Design and implement AI-assisted tools for automated reporting and real-time program visibility
  • Publish dashboards and executive reports to track progress and emerging risks
  • Set agendas, capture minutes, and track action items in team meetings
  • Maintain the CMC risk register and facilitate risk review forums
  • Partner with cross-functional teams to track commitments and ensure clarity on roles
  • Identify and pilot opportunities to modernize CMC operations with digital tools

Benefits

  • Performance-based annual cash bonus
  • Eligibility for a new hire equity grant
  • Consideration for annual equity awards based on individual performance
  • Opportunities for professional development and skills training
  • Flexible work environment to accommodate work-life balance
Full Job Description
As Intellia continues to advance its pipeline, this newly created role reflects the organization's commitment to operational excellence, scalable project management, and digital transformation within CMC. The Manager, the CMC Program Operations will serve as the operations and digital enablement lead for CMC teams, partnering directly with the Commercial CMC Team Lead to build and maintain integrated project plans, dashboards, and reporting tools that drive execution. This role goes beyond traditional project coordination, it is responsible for designing and deploying practical, generative and agentic AI-enabled tools (e.g., smart dashboards, auto-generated status reports, risk-flagging models) that improve visibility, reduce manual tracking burden, and accelerate decision-making across CMC workstreams. The Manager will drive cross-functional coordination, track program risks, manage regulatory commitment timelines, and act as the primary operations point of contact for the commercial CMC teams, with opportunity to influence broader platform and portfolio operations. Duties/Responsibilities • Build and maintain a master CMC project plan (MS Project, Smartsheet, or equivalent), identifying task interdependencies, critical path, and monitoring mechanisms for schedule risk. • Design and implement AI-assisted or automated tools (e.g., dashboard automation, natural-language status summarization, predictive risk flagging) to reduce manual reporting effort and increase real-time visibility into program health. • Publish recurring dashboards and executive-ready reporting to align the team on progress, critical path changes, and emerging risks. • Actively participate in CMC team meetings — set agendas, capture minutes, track action items, and drive follow-through. • Maintain the CMC risk register; apply a structured framework for risk identification, scoring, mitigation, and escalation, and facilitate risk review forums. • Partner with Regulatory, Process Development, Manufacturing, Supply Chain, and Quality representatives to ensure RtQ/PAC commitments are clearly defined, assigned, and tracked. • Coordinate with RegCMC on post-approval commitment (PAC) tracking and provide leadership with regular status reporting, flagging gaps or delays. • Identify opportunities to modernize CMC operations workflows through digital tools and automation; pilot and scale successful solutions across the broader CMC/pipeline organization. • Establish scalable, repeatable processes and tooling standards that improve transparency, accountability, and execution speed across CMC programs. • Lead or contribute to special projects involving process improvements, change management, and operational efficiency. Requirements Skills/Abilities • Strong project management fundamentals (MS Project, Smartsheet, or similar) with proven critical-path and risk-management experience. • Demonstrated experience using AI/automation tools to build practical operational solutions (e.g., using generative AI, low-code/no-code platforms, scripting, or BI tools like Power BI/Tableau to automate reporting, summarize data, or flag risks). • Working knowledge of GMP, quality, supply chain, and regulatory requirements in a biopharma/cell & gene therapy context. • Proven ability to influence without authority across matrixed, cross-functional teams. • Excellent written/verbal communication and stakeholder management skills. • High attention to detail, strong organizational skills, and comfort operating in a fast-paced, ambiguous environment. Education / Certifications Bachelor’s degree in a relevant field, PMP certification preferred Experience • 6+ years in biopharmaceutical/life sciences, including CMC development (cell & gene therapy preferred), with 2+ years in dedicated CMC or operations project management. • Hands-on experience building or deploying AI-enabled or automated tools to support program/operations reporting is strongly preferred Physical Requirements N/A #LI-KO1 Applications are accepted on a rolling basis, and will continue to be accepted until the position is filled at which point the position will be taken down. The base salary for this position is expected to range between $141,698.00 - $173,186.00 USD per year. The salary offered is determined based on a range of factors including, but not limited to, relevant education and training, overall related experience, specialized, rare or in-demand skill sets, internal comparators and other business needs. Upon joining Intellia, your salary will be reviewed periodically and additional factors such as time in role and performance will be considered. Intellia may change the published salary range based on company and market factors. Additional compensation includes a performance-based annual cash bonus, a new hire equity grant, and eligibility to be considered for annual equity awards the value of which are determined annually at the Company’s discretion. For more information about Intellia’s benefits, please .

About Intellia Therapeutics, Inc.

Intellia Therapeutics, Inc. is a leading genome editing company focused on developing curative therapeutics using CRISPR/Cas9 technology. The company's mission is to develop curative genome editing treatments that can positively transform the lives of patients living with severe and life-threatening diseases. Intellia's pipeline includes programs focused on genetic diseases, liver diseases, and cancer. The company was founded in 2014 and is headquartered in Cambridge, Massachusetts.
Learn more about Intellia Therapeutics, Inc.
Size
485 employees
Market Cap
$2.8 billion
Industry
Net Income
-$134.2 million
Founded
2014
5 Year Trend
+14.9%
Revenue
$57.9 million
NASDAQ

Similar Jobs

More Jobs at Intellia Therapeutics, Inc.

More Pharmaceuticals & Biotech Jobs

Find similar Manager CMC Program Operations jobs: