GMP Manufacturing Associate - Precision & Impact

Moderna; Norwood (MA); On-site; USD 54,000 - 86,000; Full time

Benefits offered by this job

Healthcare benefits

Well-being resources

Family planning benefits

Paid time off

Savings and investments

Location-specific perks

Job summary

Moderna is seeking a Manufacturing Associate in Drug Substance Operations in Norwood, MA. This hands-on role focuses on precision and routine execution in a GMP environment, producing mRNA drug substance with attention to detail.

You will follow approved procedures, support aseptic processing, and document in real time while collaborating with teammates to ensure quality and compliance. Training and gowning qualifications are required.

Qualifications

• Bachelor’s in STEM with 0–1 years or Associate with 2–4 years or high school with >4 years in a related field.
• Experience in manufacturing or regulated environments is helpful.
• Strong attention to detail and disciplined execution.
• Ability to learn technical processes and work in a GMP setting.

Responsibilities

• Execute manufacturing operations following procedures in a GMP environment.
• Perform cleanroom tasks with focus on consistency and accuracy.
• Support drug substance manufacturing activities including aseptic processing.
• Use SAP, Veeva, DeltaV, Syncade, LIMS, and CMMS as required.
• Document in real time following good documentation practices.
• Maintain cleanliness and readiness of the production area.
• Collaborate with teammates and cross-functional partners for smooth execution.
• Complete required training and maintain gowning qualifications.

Skills

Attention to detail

Discipline

Teamwork

Learning mindset

Accountability

Communication

Education

Bachelor’s degree in STEM

Associate’s degree (2–4 years)

High school diploma with >4 years experience

Tools

SAP

Veeva

DeltaV

Syncade

LIMS

CMMS

Job description

Moderna is seeking a Manufacturing Associate in Drug Substance Operations in Norwood, MA. This hands-on role focuses on precision and routine execution in a GMP environment, producing mRNA drug substance with attention to detail.

You will follow approved procedures, support aseptic processing, and document in real time while collaborating with teammates to ensure quality and compliance. Training and gowning qualifications are required.