Medical Manufacturing Associate

This is a hands-on manufacturing role for someone who takes pride in doing important work with precision, consistency, and care. As a Manufacturing Associate I in Drug Substance Operations, you will be part of the team responsible for producing mRNA drug substance in a highly controlled, regulated GMP environment. This role is a strong fit for someone who wants to build real operating capability in an environment where details matter, preparation matters, and the attention put into the quality of your work has a direct impact on our patients. Execute manufacturing operations by following approved procedures, batch records, and work instructions in a GMP-regulated environment Perform cleanroom operations with discipline, attention to detail, and a strong focus on consistency Support drug substance manufacturing activities including aseptic processing, formulation, filtration, mixing, filling, and dispensing Work within Moderna’s human performance model for error prevention, carrying out tasks with focus and accountability for accurate execution Complete documentation in real time using good documentation practices and data integrity standards Maintain the cleanliness, control, and readiness of the production area Use manufacturing systems and equipment such as SAP, Veeva, DeltaV, Syncade, LIMS, and CMMS as required Build a practical understanding of the equipment, process flow, and digital systems that support manufacturing so you can recognize issues, respond appropriately, and continue to develop and execute technical judgment Follow all safety procedures, waste handling requirements, and environmental guidelines Complete required training on time and maintain qualifications as needed for gowning and assigned operations Work closely with teammates and cross-functional partners, communicate clearly, escalate issues early, and help support smooth execution across the operation Bachelor’s degree in a STEM field with 0-1 years of relevant industry experience or Associate’s degree with 2-4 years relevant industry experience or High school diploma with more than 4 years of relevant industry experience Experience in manufacturing, operations, biopharma, life sciences, or other regulated or technical environments is helpful. An interest in a structured digital-forward advanced biomanufacturing environment is important. For this role, we are currently unable to offer immigration sponsorship. This role is 100% onsite, reflecting the importance of being physically present to support the work, collaborate closely with colleagues, and contribute to our site-based operations. Working onsite enables real-time collaboration, strong team connections, direct mentorship, and the hands-on partnership needed to deliver our mission. That’s why our benefits and well-being resources are designed to support you—at work, at home, and everywhere in between. Savings and investments to help you plan for the future 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. 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.If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.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 an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. This position may involve access to technology or data that is subject to U.As such, employment is contingent upon the applicant’s ability to access export-controlled information in accordance with U.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.