The Role Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization, working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience, with the potential to make a significant impact on patients' lives worldwide. Moderna is solidifying its presence in Norwood, Massachusetts, where science and manufacturing converge at our state-of-the-art biotechnology facilities. Our Norwood site plays a pivotal role in clinical and commercial production of our mRNA medicines and is central to Moderna’s mission. We’re seeking passionate individuals ready to contribute to cutting-edge science and scalable production in a highly collaborative environment. This opportunity offers a hands-on entry point into sterile fill-finish operations, with a focus on supporting the technical, compliance, and validation aspects of sterile drug product filling for vials and pre-filled syringes (PFS). You will work directly with senior engineers and multidisciplinary teams to ensure aseptic integrity and compliance within a highly regulated environment. You'll contribute to isolator technology processes and validation efforts, support troubleshooting of fill operations, and engage in contamination control strategies. This role provides a foundational experience in media fill design and execution, with a strong emphasis on GMP alignment, documentation, and cross-functional collaboration. It is an ideal position for individuals looking to build deep technical expertise in sterile processing while engaging with evolving technologies in support of Moderna’s mRNA platform.
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Job Type
Full-time
Career Level
Mid Level
Number of Employees
1,001-5,000 employees