Manufacturing Associate II, Research Analytics, High Throughput Operations

The Role

Moderna is seeking a Manufacturing Associate II to join Research Analytics High Throughput Operations in Cambridge MA. This hands-on role supports the reliable reproducible and timely production of DNA mRNA and Lipid Nanoparticle (LNP) materials used across Modernas research portfolio. The Manufacturing Associate II independently executes established high-throughput workflows operates manual and automated laboratory systems documents work accurately and applies process knowledge to recognize and resolve routine issues.

The successful candidate will combine strong operational discipline with scientific curiosity and a continuous-improvement mindset. They will work closely with colleagues in Research Analytics and cross-functional partners across all areas of Research to support material generation for enabling scientific advancements.

Success in this role requires strong technical execution attention to detail and the ability to work independently while balancing multiple priorities. The candidate is expected to be collaborative capable of working in a fast-paced environment uphold and maintain safe and organized laboratory operations all while delivering high-quality materials under ambitious timelines. This position is expected to work Monday through Friday 7:00 a.m.3:00 p.m.; schedule flexibility may occasionally be required to meet urgent business needs while regular working hours are subjective to change.

Heres What You Will Do:

In this role you will execute day-to-day high-throughput manufacturing activities that support the production of DNA mRNA and Lipid Nanoparticle (LNP) materials for Modernas research programs. You will prepare and process samples reagents consumables and production materials while operating both manual and automated laboratory equipment including integrated liquid-handling systems and other production instrumentation. You will accurately complete production records and digital documentation while ensuring laboratory activities meet quality safety and data integrity expectations.

You will monitor production processes identify routine process or equipment issues perform appropriate first-line troubleshooting and partner with technical experts to support investigations and issue resolution when needed. Using operational data and process knowledge you will contribute to improving workflow efficiency equipment utilization material flow turnaround time and overall laboratory performance while supporting implementation of new automation digital capabilities and operational improvements.

Working closely with colleagues across many teams such as Research Analytics Quality Control Engineering Automation Informatics you will help coordinate and execute production activities communicate priorities and production status and ensure successful handoffs between teams. As an experienced team member you will also support onboarding and task-level training of peers contribute to maintaining an organized and inspection-ready laboratory and foster a culture of collaboration accountability safety and continuous improvement.

Heres What Youll Need (Basic Qualifications)

• Associates (4 years of relevant experience) or Bachelors (2 years of relevant experience) degree in Biology Biochemistry Chemistry Biotechnology Engineering or a related scientific discipline. Equivalent combinations of education and direct manufacturing experience will also be considered.

• Hands-on experience executing laboratory or manufacturing workflows using established procedures within a quality-focused regulated or fast-paced environment.

• Experience operating laboratory instrumentation automated equipment or integrated production systems.

• Demonstrated ability to work independently manage multiple priorities and consistently deliver accurate high-quality and reproducible results.

• Strong attention to detail with experience maintaining accurate documentation and adhering to data integrity material traceability quality and laboratory safety requirements.

• Effective written and verbal communication skills with the ability to collaborate across multidisciplinary teams.

• Ability to perform hands-on laboratory work for extended periods and meet applicable laboratory gowning and physical requirements.

Heres What Youll Bring to the Table (Preferred Qualifications)

• Experience working in high-throughput automation-enabled or plate-based laboratory operations.

• Hands-on experience with Hamilton liquid handlers or comparable automated liquid-handling platforms.

• Familiarity with one or more of the following workflows: molecular DNA assembly plasmid production in vitro transcription RNA purification LNP formulation or associated analytical methods.

• Experience using laboratory digital systems electronic batch records (EBRs) Laboratory Information Management Systems (LIMS) Manufacturing Execution Systems (MES) inventory management systems or production tracking applications.

• Experience supporting process optimization Lean 5S continuous improvement laboratory organization safety or operational excellence initiatives.

• Experience using operational metrics or production data to identify workflow bottlenecks improve laboratory performance and enhance manufacturing efficiency.

• Experience onboarding training mentoring or sharing technical knowledge with peers on established laboratory or manufacturing workflows.

• Demonstrated curiosity and enthusiasm for learning new manufacturing technologies automation platforms digital tools and scientific workflows.

Working Conditions

• This is an on-site laboratory-based position in Cambridge MA.

• The role requires routine use of personal protective equipment and adherence to laboratory gowning safety and waste-handling procedures.

• The role may require standing for extended periods repetitive pipetting or material-handling activities and occasional lifting consistent with site requirements.

• Occasional schedule adjustments or overtime may be needed to support critical production activities.

Pay & Benefits

At Moderna we believe that when you feel your best you can do your best work. Thats why our benefits and well-being resources are designed to support youat 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 planning benefits including fertility adoption and surrogacy support
• Generous paid time off including vacation 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 salary range for this role is $63200.00 - $100900.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individuals position within the salary range will be based on several factors including but not limited to specific competencies relevant education qualifications certifications experience skills performance and business or organizational needs. The successful candidate may be eligible for an annual discretionary bonus other incentive compensation or equity award subject to company plan eligibility criteria and individual performance.

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.

If you want to make a difference and join a team that is changing the future of medicine we invite you to visit to learn more about our current opportunities.

Our Working Model

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.

Moderna is a smoke-free alcohol-free and drug-free work environment.

Equal Opportunities

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a persons 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 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 an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories consistent with legal requirements.

Accommodations

Were 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 accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation 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 team at .

Export Control Notice This position may involve access to technology or data that is subject to U.S. export control laws including the Export Administration Regulations (EAR). As such employment is contingent upon the applicants ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements only individuals who qualify as U.S. persons (citizens permanent residents asylees or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license. #LI-NH1

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