Senior Packaging & Labeling Specialist — GMP, ALCOA+

Moderna Therapeutics; Norwood (MA); Hybrid; USD 74,000 - 118,000; Full time

Benefits offered by this job

Healthcare benefits

Well-being resources

Family planning benefits

Paid time off

Retirement savings plan

Job summary

Moderna Therapeutics is seeking a Sr. Manufacturing Associate I, Drug Product Label & Packaging to execute cGMP labeling and packaging for parenteral presentations (vials and prefilled syringes).

You will perform line setup, changeovers, line readiness checks, and ensure label control and reconciliation with ALCOA+ documentation. The role requires 3–5 years GMP manufacturing experience, a High School diploma or GED, ability to lift ~35 lbs, and collaboration with QA/QC, Engineering, and Supply

Qualifications

• 3–5 years of experience in GMP manufacturing or regulated operations.
• Demonstrated ability to independently execute routine and complex packaging tasks with accurate documentation.
• Strong ALCOA+ documentation and line-clearance habits.
• Ability to train and coach peers and escalate issues when needed.

Responsibilities

• Lead and/or execute line setup, operation, and changeovers for labeling and packaging.
• Perform line clearances, room/equipment readiness checks, and material staging.
• Execute label control activities: issuance, use, return, reconciliation, disposition.
• Conduct in-process checks and verification steps (barcode, vision, print/scan).
• Maintain accurate contemporaneous documentation (logbooks, batch records, MES).
• Escalate deviations and assist with shift-level investigations and CAPAs.

Skills

GMP Manufacturing Experience

ALCOA+ Documentation

Team Collaboration

Education

High School Diploma or GED

Associate/Bachelor preferred

Job description

Moderna Therapeutics is seeking a Sr. Manufacturing Associate I, Drug Product Label & Packaging to execute cGMP labeling and packaging for parenteral presentations (vials and prefilled syringes).

You will perform line setup, changeovers, line readiness checks, and ensure label control and reconciliation with ALCOA+ documentation. The role requires 3–5 years GMP manufacturing experience, a High School diploma or GED, ability to lift ~35 lbs, and collaboration with QA/QC, Engineering, and Supply