(Fixed Term) Manufacturing Associate

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.

Based at our Clayton manufacturing site, you'll play a vital role in producing mRNA vaccines that make a meaningful difference for patients. Working in a highly advanced manufacturing environment, you'll combine technical expertise, digital capability, and scientific thinking to deliver high-quality products while continuously improving the way we operate.

This fixed-term opportunity is ideal for someone who thrives in a fast-paced GMP environment, enjoys learning new technologies, and is motivated by operational excellence, collaboration, and innovation—including opportunities to work alongside advanced digital and Generative AI-enabled tools that support modern manufacturing and continuous improvement.

Here's What You'll Do

• Operate manufacturing equipment to safely produce mRNA vaccines in accordance with cGMP requirements, standard operating procedures, and manufacturing documentation.
• Practice safe work habits while adhering to Moderna's safety procedures, guidelines, gowning requirements, and housekeeping standards.
• Execute manufacturing activities with precision while maintaining exceptional attention to detail.
• Partner closely with Quality Assurance colleagues to complete batch documentation supporting the timely disposition of commercial product.
• Apply operational performance tools and collaborate with teammates to achieve manufacturing KPI objectives.
• Rapidly troubleshoot routine equipment, process, and digital issues to maintain reliable operations.
• Proactively identify and escalate compliance, quality, health, or safety issues to the Manufacturing Supervisor.
• Participate in incident investigations, root cause analysis (RCA), and CAPA activities.
• Maintain accurate training records and associated documentation.
• Perform routine basic equipment maintenance, including lubrication, mechanical checks, and filter changes using hand tools.
• Contribute to multiple projects and continuous improvement initiatives within a dynamic manufacturing environment.
• Collaborate effectively across cross-functional teams to support manufacturing excellence.
• Work rotating shift patterns, including afternoon and night shifts, weekends, public holidays, overtime, and roster adjustments based on production requirements.

We're looking for someone who brings

• Typically 3–5+ years' experience within a GMP manufacturing environment.
• A college degree specializing in Pharmaceutical Production Technology or an equivalent discipline.
• Aseptic manufacturing and visual inspection experience (preferred).
• Experience supporting audits and inspections with a sound understanding of health authority and regulatory expectations.
• Strong collaboration skills with peers, leaders, and cross-functional partners.
• Excellent written, verbal, organizational, and communication skills.
• The ability to manage multiple priorities while maintaining meticulous attention to detail with minimal supervision.
• Digital confidence and enthusiasm for working with advanced manufacturing technologies, automation, and emerging digital capabilities.
• A scientific mindset, strong learning agility, and a passion for continuous improvement.
• Availability to work full-time on site at our Clayton manufacturing facility, supporting a 24/7 operation through rotating shifts.
• English language proficiency to support global collaboration.
• Willingness to participate in pre-employment and periodic medical assessments where required for workplace health and safety.

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

• We obsess over learning. We don’t have to be the smartest we have to learn the fastest.
• We digitize everywhere possible using the power of code to maximize our impact on patients.

Here’s What You’ll Need (Basic Qualifications)

• 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 and Visual Inspection experience preferred
• 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
• Demonstrated ability and willingness to work across rotating shifts, including afternoon and night shifts, in a 24/7 manufacturing environment
• This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work
• Proficiency in English (verbal and/or written) required due to global collaboration needs
• 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.

Pay & Benefits

At Moderna, we believe that when you feel your best, you can do your best work. That’s why our benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.

• Competitive healthcare, 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 building benefits, including fertility, adoption, and surrogacy support
• Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
• Savings and investments to help you plan for the future
• 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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