Manufacturing Associate II

The Role:

This Manufacturing Associate II DP Operations builds on core cGMP experience performing routine unit operationsincluding formulation filtration aseptic filling within isolators and downstream visual inspection. This role ensures material and component readiness performs enhanced in-process controls and keeps equipment within defined parameters while documenting contemporaneously in MES/eBR. The associate works under moderate supervision and contributes to operational efficiency through adherence to SOPs collaboration across functions and active participation in a clean and compliant manufacturing environment. Success is measured by plan attainment documentation accuracy right-first-time execution and effective knowledge sharing.

Heres What Youll Be Doing:

• Perform formulation sterile filtration vial/syringe filling and visual inspection in accordance with SOPs and cGMP requirements.

• Conduct equipment checks material staging aseptic line clearances and routine facility/equipment cleaning using approved disinfectants.

• Complete accurate contemporaneous and compliant ALCOA documentation including logbooks and electronic batch record (eBR) entries.

• Perform required in-process checks accurately record results and ensure compliance with established specifications and procedures.

• Identify and promptly escalate deviations atypical events and equipment issues; support troubleshooting and investigations by providing relevant data and statements.

• Support the development and revision of SOPs and work instructions and implement continuous improvement opportunities.

• Maintain strict adherence to cGMP gowning aseptic behavior safety and documentation requirements while maintaining a clean and safe operating environment.

• Complete required training maintain qualifications and skills matrices and train/mentor peers to support team capability and compliance.

• Collaborate effectively with QA QC MS&T Facilities Supply Chain and other cross-functional partners during routine operations and issue resolution.

• Work effectively in a fast-paced cross-functional manufacturing environment demonstrating flexibility to support cross-training operational coverage off-hours and overtime as needed.

Heres What Youll Need (Basic Qualifications):

• Associates or Bachelors Degree in a Scientific field or a High School Diploma with equivalent experience.

• 2-4 years in GMP manufacturing or similar environment preferred; we will train strong entry-level candidates.

• Comfortable working in cleanrooms with full gowning and standing for extended periods; able to lift up to 35 lbs.

• Basic computer skills (batch records training systems).

• Must have 20/20 vision (corrected vision allowed i.e. glasses contact lens) and maintain the ability to see all colors across the visible spectrum. A vision test will be required upon hiring to confirm vision acuity and will be administered annually thereafter.

• Reliable detail-oriented follows instructions communicates clearly and works well on a team.

• This position requires availability to work a 12-hour night shift from 6:00 PM to 6:00 AM including flexibility to support operational coverage cross-training overtime weekends and holidays as business needs require.

Our Working Model

As we build our company we have always believed that an in-person culture is critical to our success.

This role is 100% onsite reflecting the importance of being physically present to support the work collaborate closely with colleagues and contribute to our site-based operations.

Working onsite enables real-time collaboration strong team connections direct mentorship and the hands-on partnership needed to deliver our mission. 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.

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.

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.

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Required Experience:

IC