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. 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. In this role, you will be responsible for executing processing and combining mRNA and LMX/LNP for clinical pipeline products as well as commercial seasonal vaccines in a GMP-regulated environment. You will act as a technical resource for the clinical and commercial drug substance manufacturing team, applying fundamental and developing knowledge of bioprocess unit operations, process engineering, and digital systems. This role requires participation in the development of operational procedures and training materials, training of manufacturing associates, technology transfer support, and issue investigations while ensuring the progress monitoring of projects. Here’s What You’ll Do Your key responsibilities will be: Ensuring compliance with GMP regulations, guidelines, and company policies. Promoting safe work habits and adherence to safety procedures. Executing tasks precisely as per Standard Operating Procedures (SOPs) and work instructions. Maintaining Good Documentation Practices and Data Integrity for regulatory use. Completing required training and requalification within the prescribed timelines. Utilizing manufacturing support systems such as SAP, VEEVA, Delta V, Syncade, LIMS, and CMMS. Your responsibilities will also include: Acting as a Qualified Trainer, conducting On-the-Job Training (OJT) for eBR review and unit operations. Coaching the manufacturing team in process execution, troubleshooting, cGMPs, and safety practices. Supporting technology transfers, cross-functional projects, and manufacturing operations. Collaborating with process Subject Matter Experts (SMEs) to develop batch records, SOPs, and training materials. Partnering with QA colleagues to ensure timely batch disposition, deviation investigations, and compliance reviews. Managing equipment Out of Tolerance (OOT) responses and implementing CAPAs for deviations. Leading change controls for team projects. Handling purchasing and induction of simple equipment and tools. Participating in equipment start-up, commissioning, and validation activities. The key Moderna Mindsets you’ll need to succeed in the role: We behave like owners – You will take responsibility for process execution, troubleshooting, and problem-solving, ensuring that the solutions you implement improve operations beyond just your role. We digitize everywhere possible – This role requires proficiency in digital systems such as SAP, Delta V, and LIMS, ensuring seamless execution and data integrity in a highly regulated environment. Here’s What You’ll Need (Basic Qualifications) STEM degree with 3-5 years’ industry experience or a Masters’ degree with 1-2 years’ industry experience This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work. Here’s What You’ll Bring to the Table (Preferred Qualifications) Strong understanding of GMP regulations. A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative. Moderna offers personalized benefit programs and well-being resources as unique as our global workforce: Quality healthcare and insurance benefits Lifestyle Spending Accounts Free premium access to fitness, nutrition, and mindfulness classes Family planning and adoption benefits Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown Educational resources Savings and investments Location-specific perks and extras The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work. 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. Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.