Engineer III, MSAT

BS, M.S. or Ph.D. in a technical discipline related to Pharmaceutical Manufacturing (Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Engineering, etc.).  BS with 5 to 8 years of experience or MS with 2 to 5 years experience in a pharmaceutical or biotechnology company.

Experience in cGMP manufacturing operations.

Knowledge of data management tools and statistical analysis.

Excellent judgment and ability to communicate manufacturing issues in a scientifically sound and understandable way along with ability to provide data driven solutions.

A highly collaborative team player capable of working in a cross-functional matrix environment.

Ability to manage projects in a fast-paced environment.

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

Best-in-class healthcare coverage, 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 investment opportunities to help you plan for the future

Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.

Moderna is strengthening its presence in Norwood, Massachusetts, a cornerstone of our manufacturing and operational excellence. Our Norwood campus translates mRNA science into scalable impact, supporting the global delivery of our medicines. We welcome talent ready to drive innovation and make a meaningful difference for patients worldwide.

In this role, you will serve as a technical leader, driving the development, implementation, and optimization of RNA, lipid nanoparticles (LNP), and DNA (synthetic and E. coli) manufacturing to support clinical and commercial programs.

Operating as a highly visible individual contributor, you will lead from the manufacturing floor while shaping process strategy, ensuring robust GMP execution, and enabling scalable, high-performance technology transfers.

You will play a critical role in advancing manufacturing through data-driven insights, continuous improvement, and the integration of digital and AI-enabled tools to enhance process robustness and efficiency.

Here's What You'll Do:

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.