Director, Product Owner

The Role

The CMC Director, Product Owner leads product lifecycle management, value chain, launch planning and supply chain operations oversight for mFLUSIVA, mCOMBRIAX and mRESVIA. The role connects global portfolio and supply strategies with country execution, ensuring launches and lifecycle changes are delivered in a coordinated, compliant and supply-ready manner while maintaining reliable day-to-day performance.

You will play a pivotal role in ensuring that our Global Supply Chain (GSC) strategy is aligned with the company’s ambitions of delivering innovative mRNA medicines to the market. You will serve as the leader of the Product team and lead an integrated team responsible for planning, launching, and managing the life cycle of various products. This role requires a strong understanding of supply chain processes, collaboration across CMC functions, an enterprise collaboration mindset and a deep commitment to operational excellence and continuous improvement.

As Product Owner, you are accountable for post-launch product lifecycle leadership, integrating CMC commercialization, value stream performance, lifecycle risk and KPI management, global expansion, variations, manufacturing network resilience, and end-to-end supply readiness across the commercial lifecycle.

Here’s What You’ll Do

• Own the integrated product lifecycle and commercialization agenda across markets, indications, presentations, launches, regulatory changes, transfers, variations and discontinuations, translating global portfolio and commercial strategies into clear requirements, milestones, dependencies, decisions and accountable owners.

• Establish and lead cross-functional lifecycle and launch governance across CMC, including stage gates, readiness criteria, Commit-to-File/Commit-to-Launch processes, launch coordination and integration into long-range planning, IBP, Product Phase S&OP/S&OE and country operating plans.

• Lead CMC commercialization strategy and readiness, translating market and patient/customer needs into product configurations, SKU strategy, launch sequencing, delivery models and executable cross-functional plans.

• Own the end-to-end product value chain strategy and roadmap, including value-stream maps, current and target conditions, performance metrics, improvement priorities, and physical, information/document and financial flows.

• Drive product supply-chain and manufacturing network strategy and resilience, including network footprint, multi-site manufacturing and packaging configurations, capacity flexibility, intercompany/product-ownership flows, tax/tariff considerations and disruption/scenario readiness.

• Integrate clinical and commercial supply planning across the product lifecycle, ensuring demand visibility, inventory strategy, planning and master-data readiness, reliable supply-chain operations, and effective transition from launch to steady-state commercial supply.

• Own post-launch product performance and risk management, including the product risk register, success metrics/KPIs, mitigation plans, performance gaps and escalation of key risks and decisions through appropriate leadership forums.

• Lead post-launch CMC regulatory lifecycle and variation management (Including ASU for 1010 & 1083), including RTQs, global expansion readiness, market commitments and health authority responses, partnering with the Variation Office and functional teams and applying the agreed Product Lead/Product Owner ownership model.

• Own commercial product image and lifecycle readiness, coordinating global and local artwork, labeling and packaging configurations, manufacturing-site implementation, change control, serialization/traceability, master data and supply readiness.

• Act as the CMC/Product Team leader and representative in enterprise forums, driving cross-functional decision-making, governance, financial planning and alignment across CMC, Commercial, Regulatory and Supply Chain.

• Lead communication and coordination of major product lifecycle activities, including launches, tech transfers, network changes and other cross-functional product initiatives, ensuring clear ownership, dependencies and timely execution.

• Drive operational excellence and continuous improvement, using lifecycle learnings, data, benchmarking and value-stream performance to establish reusable standards and improve product and supply-chain performance.

• Additional duties as may be assigned from time to time.

Here’s What You’ll Need (Basic Qualifications)

• Education: A bachelor’s degree in a relevant field (e.g., Supply Chain Management, Life Sciences, and/or Engineering)

• Experience: 12+ years of experience in the pharmaceutical or biotech industry, with a focus on Supply Chain, CMC Program Management, Value Chain Leadership, or similar roles. Experience in CMC commercialization and an understanding of value creation within the biopharmaceutical industry.

Here’s What You’ll Bring to the Table (Preferred Qualifications)

• Ability to lead and inspire cross-functional teams, fostering an inclusive and innovative environment.

• Proven track record of aligning supply chain strategies with broader business goals to drive impactful long-term solutions.

• Strong analytical skills to synthesize data, enabling informed decision-making and optimization of operations.

• Adaptability in dynamic environments, excelling under pressure while driving continuous improvements.

• Clear and concise communication with stakeholders, ensuring alignment on strategic initiatives and objectives.

• A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

Our Working Model 

As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.

Moderna is a smoke-free, alcohol-free, and drug-free work environment.

Pay & Benefits

At Moderna, we believe that when you feel your best, you can do your best work. That’s why our benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.

• Competitive healthcare, plus voluntary benefit programs to support your unique needs
• A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
• Family planning benefits, including fertility, adoption, and surrogacy support
• Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
• Savings and investments to help you plan for the future
• Location-specific perks and extras

The salary range for this role is $167,000.00 - $300,700.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual’s position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs. The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.  

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities. 

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. 

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. 

Equal Opportunities

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law.  Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. 

Accommodations

We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best. 

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at leavesandaccommodations@modernatx.com. 

Export Control Notice This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant’s ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license.

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