Sr. Manufacturing Associate I, Label & Packaging

The Associate I Drug Product Label & Packaging is an experienced hands-on operator and shift resource supporting cGMP labeling and packaging operations for Modernas parenteral drug product presentations including vials and prefilled syringes. This role independently executes routine and complex packaging activities supports and may lead line readiness and changeovers maintain disciplined label control and reconciliation and serves as a reliable troubleshooting and escalation resource during daily operations.

This position emphasizes accuracy right-first-time execution strong documentation habits (ALCOA) timely escalation and collaboration to ensure packaged products meet quality regulatory serialization and market requirements. Success looks like consistent independent execution effective peer coaching strong ownership of line performance and growing leadership across safety quality documentation and throughput.

Execute packaging operations per approved SOPs and cGMPs including (as qualified/assigned):

• Lead and/or execute line setup operation and changeover activities for labeling and packaging processes (e.g. label application cartoning kitting aggregation/case packing where applicable) ensuring correct configuration and readiness prior to start.
• Perform and verify line clearances room/equipment readiness checks and controlled material/component staging to support compliant operations and minimize mix-ups.
• Execute and verify label control activities including label issuance/use/return segregation reconciliation and disposition support per procedure; ensure counts and documentation are accurate and complete.
• Conduct and document in-process checks and inspection/verification steps (e.g. barcode/label verification vision checks print/scan verification where applicable) and take appropriate action within procedures.
• Complete accurate contemporaneous documentation (ALCOA) including logbooks batch record entries and electronic transactions (MES/eBR/labeling systems as applicable); review own work and support peer review for completeness and accuracy.
• Verify equipment status/readiness including calibration labels PM tags cleaning status and required pre-use checks; escalate gaps before processing begins.
• Identify contain and escalate deviations atypical events and equipment/system issues; perform intermediate troubleshooting within training and follow escalation pathways to reduce downtime and maintain compliance.
• Support shift-level investigation activities CAPAs and change controls for packaging-related events by providing factual timelines observations and clear documentation; may support implementation of corrective actions on the floor.
• Train coach and support qualification of associates through structured OJT peer guidance and demonstration of proper technique; promote consistent execution cGMP behaviors and safe work practices.
• Maintain compliance with gowning requirements (as applicable) controlled-area behaviors safety protocols and 5S/housekeeping standards; model safe and compliant behaviors for the team.
• Collaborate effectively with cross-functional partners during routine and non-routine operations (QA/QC MS&T Engineering Supply Chain Digital/Systems) including support of equipment readiness engineering runs and process improvement activities.
• Participate in and support continuous improvement activities related to safety quality documentation throughput reconciliation and line performance.
• Flexibility to work off-hours weekends overtime and different shifts as needed to meet production demands and business needs.

• High School Diploma / GED required; Associates or Bachelors degree in a scientific/technical field preferred (or equivalent experience).
• Typically 3-5 years of experience in GMP manufacturing or regulated operations; labeling/packaging experience in pharma/biotech strongly preferred.
• Demonstrated ability to independently execute routine and complex work while maintaining strong documentation practices (ALCOA).
• Experience with packaging batch records line clearance in-process checks label control/reconciliation and basic to intermediate equipment/system troubleshooting preferred.
• Ability to support training peer coaching escalation and shift-level problem solving in a compliant manufacturing environment.
• Comfort working in controlled environments with standing for extended periods following gowning/PPE requirements and performing repetitive tasks with high attention to detail.
• Ability to lift up to 35 lbs (or per site standard) and perform physical tasks consistent with packaging operations.

• Working knowledge of cGMP expectations ALCOA principles packaging batch records logbooks and electronic manufacturing/labeling systems.
• Strong attention to detail with disciplined documentation reconciliation and line-clearance habits.
• Clear communication skills with the ability to escalate issues promptly and provide accurate handoffs.
• Ability to work effectively in a team environment and serve as a positive peer resource for newer associates.
• Demonstrated ownership mindset reliability flexibility and commitment to safety quality and continuous improvement.

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 $74000.00 - $118400.00. 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-SB2

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