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's mission is to establish a leading-edge research, development, and manufacturing facility at Harwell, as part of a long-term commitment to onshore mRNA vaccine production for respiratory diseases. This initiative will create a multitude of highly skilled jobs and foster collaboration with academic, NHS, and government partners across the UK. We're looking for global experts eager to join us in this endeavor, contributing to a future where access to life-saving vaccines is a reality for all. 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. Your work will directly impact our ability to deliver high-quality mRNA medicines efficiently and effectively. We digitize everywhere possible – As Moderna continues to push the boundaries of digital and automated manufacturing, 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. At Moderna, we believe that when you feel your best, you can do your best work. That’s why our global benefits and well-being resources are designed to support you—at work, at home, and everywhere in between. Quality healthcare and insurance benefits Lifestyle Spending Accounts to create your own pathway to well-being 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, global recharge days, and a discretionary year-end shutdown 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. 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. As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact. 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. Moderna is a smoke-free, alcohol-free, and drug-free work environment. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply Moderna is committed to equal opportunity in employment 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. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best. Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at leavesandaccommodationsmodernatx.com. LI-JP1 -