Senior Labeling & Packaging Operator (GMP)

Moderna; Norwood (MA); On-site; USD 74,000 - 118,000; Full time

Benefits offered by this job

Healthcare benefits

Well-being resources

Family planning benefits

Generous PTO and holidays

Savings & investments

Location-specific perks

Job summary

Moderna is seeking a Sr. Manufacturing Associate I, Drug Product Label & Packaging to support cGMP labeling and packaging for parenteral drug products, including vials and prefilled syringes.

You will perform line setup, changeovers, and material staging with accuracy and strong documentation. This role emphasizes independence, ownership of line performance, and coaching peers, while collaborating with QA/QC, MS&T, Engineering, and Supply Chain to ensure compliant, high-quality packaged

Qualifications

• High School Diploma or GED required; scientific/technical degree preferred.
• Typically 3–5 years of GMP manufacturing or regulated operations.
• Experience in labeling/packaging in pharma/biotech is strongly preferred.
• Excellent documentation habits (ALCOA+).

Responsibilities

• Lead/execute line setup, operation, and changeovers for labeling and packaging.
• Perform line clearances, material staging, and readiness checks.
• Manage label control activities and reconciliation per procedure.
• Document in-process checks and ensure accuracy of records (ALCOA+).
• Escalate deviations and support shift-level investigations and CAPAs.
• Coach associates and support qualification through structured OJT.
• Maintain gowning, safety, 5S, and cross-functional collaboration.

Skills

ALCOA+ documentation

GMP manufacturing

Troubleshooting

Line readiness

Education

High School Diploma / GED

Scientific/technical degree preferred

Tools

MES / eBR / labeling systems

Job description

Moderna is seeking a Sr. Manufacturing Associate I, Drug Product Label & Packaging to support cGMP labeling and packaging for parenteral drug products, including vials and prefilled syringes.

You will perform line setup, changeovers, and material staging with accuracy and strong documentation. This role emphasizes independence, ownership of line performance, and coaching peers, while collaborating with QA/QC, MS&T, Engineering, and Supply Chain to ensure compliant, high-quality packaged