• Job Description

  Req#: R17931

  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.

  We are seeking a hands-on, digitally fluent Manufacturing Associate to support Moderna’s mRNA vaccines production unit at our Clayton site. This role is at the forefront of scientific innovation and operational execution, demanding excellence in process execution, digital acumen, and collaboration.

  
  You will operate state-of-the-art production equipment under GMP compliance, ensuring the safe and efficient production of life-changing vaccines.

  
  The ideal candidate is analytical, precise, and thrives in high-tech environments. A scientific mindset and comfort with digital systems are essential, as is the ability to adapt quickly to evolving technology.
  You will be actively engaged in continuous improvement and expected to maintain meticulous documentation and production practices.

  
  This role is embedded in our commitment to operational excellence, ensuring that Moderna’s mission of delivering transformative mRNA medicine reaches patients safely and swiftly.
  You will also contribute to a culture of safety, learning, and innovation while collaborating with QA and operations peers.

  
  The position requires flexibility, cross-functional engagement, and a readiness to embrace change in a highly dynamic manufacturing context.
  It is ideal for someone who values detailed execution, digital innovation, and meaningful impact on public health.

  
  Please note: this is a site-based position located in Clayton, and is not eligible for remote work.

  Here’s What You’ll Do:

  Your key responsibilities will be:

  • Operating production equipment safely and in strict adherence to cGMP guidelines and Moderna procedures

  • Practicing and promoting safety protocols and personal protective measures in all operations

  • Executing operations as per current Good Manufacturing Practices (cGMP), standard operating procedures (SOPs), and batch documentation

  • Maintaining compliance through accurate training records and associated documentation

  • Carrying out routine basic maintenance of equipment including lubrication and mechanical checks using hand-tools

  • Responding to and troubleshooting process and digital issues swiftly

  • Supporting QA teams by facilitating timely closure of required documentation for batch disposition

  • Applying operational performance tools to drive manufacturing KPI outcomes

  • Participating in cross-functional projects and driving process improvement initiatives

  Your responsibilities will also include:

  • Reporting and escalating compliance or safety concerns proactively

  • Participating in Root Cause Analyses (RCA) and corrective and preventive action (CAPA) processes

  • Maintaining proper gowning and cleanliness standards in assigned areas

  • Flexibly supporting off-hours operations and overtime as necessary

  • Collaborating effectively across a cross-functional matrixed team environment

  • Adapting rapidly to evolving production technologies, with a mindset focused on innovation and continual learning

  • Contributing to Moderna’s mission through detailed execution and ownership of operational processes

  The key Moderna Mindsets you’ll need to succeed in the role:

  • We digitize everywhere possible using the power of code to maximize our impact on patients.
    This mindset directly aligns with the digitally fluent environment in which you will work. Your comfort with digital systems and commitment to tech-forward solutions will enable our high-velocity, high-integrity operations.

  • We behave like owners. The solutions we’re building go beyond any job description.
    You will be expected to own your processes, your documentation, and your commitment to quality. This mindset fuels a sense of responsibility and proactive engagement essential in GMP manufacturing.

  Here’s What You’ll Bring to the Table:

  • Typically, 3-5+ years of experience in a GMP manufacturing environment

  • A College degree with a specialization in Pharmaceutical production technology or equivalent

  • Aseptic experience, Visual Inspection and PFS knowledge

  • Experience in audit / inspection preparation, understanding Health authority and regulatory guidelines

  • Ability to collaborate fluidly with peers, leadership and cross-functional support groups required

  • Excellent written, oral communication, and organizational skills required.

  • Ability to maintain attention to detail while executing multiple tasks with minimal supervision

  • Demonstrated commitment to Moderna's values of Bold, Collaborative, Curious, and Relentless, embodying these values in the workplace

  • As part of Moderna’s commitment to workplace health and safety, this role may be subject to pre-employment and periodic medical assessments, in line with relevant legal and operational requirements.

  • This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work.

  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 leavesandaccommodations@modernatx.com.

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• About the company

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