Moderna Job Trends

In this role, you will be responsible for executing and supporting daily operations related to component preparation, formulation, and aseptic filling . This role ensures consistent execution aligned with cGMP standards, operational procedures, and right-first-time performance. The MA II maintains a strong presence on the manufacturing floor to provide coaching, support issue resolution, and contribute to batch success. This individual is accountable for documentation ownership, SOP and MES alignment, training, and quality record management. While focused on hands-on operations, the MA II is also expected to lead activities when required , particularly during media fills, tech transfers, product introductions ,...

Moderna is seeking a Sr. Manager, Medical Publications to lead the development and execution of publication activities across multiple therapeutic areas. This role will focus on collaborating with internal and external authors and cross-functional teams - including Medical, Research, Development, CMC, HEOR, and external vendors - to develop and execute comprehensive publication plans. Key responsibilities include creating and implementing publication plans, managing copyright permissions, tracking publication metrics, and ensuring timely and accurate completion of activities within the publication system of record. Key responsibilities include managing publication plans and metrics, overseeing copyright permissions, ensuring adherence to global and regional guidelines, and...

The Director, Global Regulatory Science CMC will be responsible for leading regulatory CMC activities for one or more products, depending on complexity, through all stages of a product’s lifecycle. The Director will manage a small group of individuals responsible for developing global regulatory CMC strategies and collaborating with key stakeholders to execute the strategies in alignment with business priorities. The Director will be expected to provide guidance to the product teams supporting products in their portfolio. In addition, the individual will be responsible for preparation, review, and approval of CMC and Quality related Health Authority correspondence and regulatory applications. The...

Moderna is seeking a motivated and energetic Associate Director level project manager responsible for providing project management leadership to enable execution of cross-functional process building and improvement projects across the Development organization. This position will play a role in helping to establish a centralized function that will drive critical strategic projects, support building a continuous improvement capability that will enable the Development organization to scale as we look to establish key internal capabilities in support of operational excellence in our clinical trials and deliver on the promise of mRNA technology. This role will be responsible to develop strong oversight and...

ModernaTX, Inc. seeks a Senior Engineer II, MST for its Norwood, Massachusetts location. Here’s What You’ll Do Lead technical transfer and new process implementation to ensure the robust production of mRNA and lipid nanoparticle (LNP) drug substances using current Good Manufacturing Practices (cGMP). Work collaboratively with cross functional stakeholders including technical development, manufacturing, automation, regulatory, and quality, to ensure all technical aspects of the process are successfully implemented. Collaborate with technical development and process development of mRNA and LNP on material generation for Investigational New Drug (IND) enabling studies. Provide technical support and serve as the subject matter expert for...

In this role, you will be responsible for leading regional implementation projects, knowledge dissemination, and integration initiatives that aim to improve patient outcomes and public health management. Within this field-based role, the Implementation Science Lead (ISL) will build the peer-to-peer relationship and identify new partnership opportunities with regional experts within IDNs and academic medical centers. In addition, the ISL will work with diverse professional teams to assess gaps and unmet medical needs and lead collaborative studies, develop evidence-based educational programs, and evaluate the impact of these interventions on patient outcomes and public health objectives. The day-to-day work will include protocol...

We are seeking an experienced and versatile IT/OT Systems Engineer to support and maintain both the infrastructure and application layers of our manufacturing environment. This role is ideal for a technically adept professional who thrives at the intersection of Information Technology and Operational Technology—able to switch from troubleshooting server and network issues one day, to resolving MES or DeltaV system problems on the manufacturing floor the next. Able to work closely with Digital Core teams like cybersecurity and enterprise technologies, to manufacturing operators and plant management. You will play a key role in ensuring the reliable operation of systems critical...

We are seeking an experienced and dynamic Principal Software Engineering Manager to lead an organization of software engineering teams focused on the development of internal applications and integrations with third-party tools and vendors. This role is critical to providing technical and people leadership to the engineers in the digital for CMC/technical development organization as well as providing a strategic outlook of engineering activities to digital leadership. The Principal Software Engineering Manager will manage teams based in Norwood, MA and Cambridge, MA. Here’s What You’ll Do Lead the development, deployment, and maintenance operations of cloud-based (AWS) scientific software systems, as well...

Within an end-to-end (E2E) labeling framework, manage a team of labeling strategy leads responsible for, in partnership with the GRS Strategy team, ensuring the development and implementation of regulatory labeling strategies to meet Moderna’s company objectives and the needs of patients. This leader closely partners with the GRS Head of Labeling Operations and other Regulatory functions as well as stakeholders in Clinical Development, Commercial, Legal, Medical, Pharmacovigilance and others to ensure the timely creation, revision, and submission of compelling and compliant labeling. Here’s What You’ll Do Labeling Responsibilities for Assigned Products Provide regulatory expertise and guidance to internal stakeholders for...