Associate I, Quality Control Microbiology EMCU

ModernaTX • Norwood, MA

13d • Onsite

About The Position

The Role: 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 be responsible for executing critical environmental monitoring and utility sampling that ensures the integrity of GMP manufacturing environments. You will generate and manage high-quality microbiological data that directly supports both clinical and commercial production. This is a hands-on opportunity to deepen expertise in QC microbiology while leveraging digital systems like LIMS and gaining exposure to emerging technologies, including Generative AI, to enhance data trending and quality insights. The key Moderna Mindsets you’ll need to succeed in the role: “We act with urgency; Action today compounds the lives saved tomorrow.” “We digitize everywhere possible using the power of code to maximize our impact on patients.”

Requirements

• Education: Degree
• Experience: STEM degree with 0+ years’ of experience in a GMP QC laboratory setting, focusing on microbiology.
• Specific Certifications or Training: None

Nice To Haves

• Hands-on experience with particle counters, viable air samplers, and gas equipment.
• Proficiency with Microsoft Office Programs and electronic databases (LIMS, SAP, eQMS).
• Excellent troubleshooting skills and the ability to communicate scientific issues clearly.
• Strong written and oral communication skills and organizational abilities.
• Knowledge of GMP, microbiology, aseptic techniques, and general laboratory instrumentation.
• Ability to work effectively in a fast-paced, cross-functional matrix environment.
• Familiarity with relevant FDA, EU, ICH guidelines, and regulations
• Bold, Relentless, Curious, and Collaborative.

Responsibilities

• Conduct Environmental Monitoring (routine, in-process, and EMPQ’s) within GMP manufacturing environments
• Perform Water for Injection (WFI) sampling and compressed gas sampling to support critical utility monitoring
• Maintain laboratory equipment and execute routine housekeeping to ensure compliance and operational readiness
• Author, revise, and follow SOPs, protocols, and technical reports with precision
• Ensure accurate data entry, review, and trending within LIMS to support data integrity and regulatory compliance
• Collaborate with internal and external laboratories to coordinate sample management and testing activities
• Troubleshoot laboratory equipment and microbiological test methods to maintain continuity and reliability of results
• Support quality systems documentation, including deviations, change controls, and CAPAs
• Participate in audits and contribute to continuous improvement initiatives across QC operations
• Train on microbiology laboratory techniques and assays associated with critical utilities testing, including bioburden and endotoxin

Benefits

• 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
• Location-specific perks and extras

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 1,001-5,000 employees