GMP Manufacturing Associate I – Onsite, Detail‑Driven

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

Benefits offered by this job

Competitive healthcare

Well‑being resources

Family planning benefits

Paid time off

Savings & investments

Location‑specific perks

Job summary

Moderna is seeking a hands‑on Manufacturing Associate I in Drug Substance Operations to join a highly controlled GMP environment. You will perform aseptic processing, operate with precision, and ensure data integrity while supporting multi‑step production processes for mRNA drug substance.

The role emphasizes adherence to safety, training, and continuous improvement, with a strong focus on teamwork and high‑quality output that directly impacts patient care.

Qualifications

• Bachelor’s degree in a STEM field with 0‑1 years of relevant industry experience or Associate’s degree with 2‑4 years relevant industry experience or High school diploma with more than 4 years of relevant industry experience
• Experience in manufacturing, operations, biopharma, life sciences, or other regulated or technical environments is helpful. An interest in a structured digital‑forward advanced biomanufacturing environment is important.

Responsibilities

• Execute manufacturing operations by following approved procedures, batch records, and work instructions in a GMP‑regulated environment
• Perform cleanroom operations with discipline, attention to detail, and a strong focus on consistency
• Support drug substance manufacturing activities including aseptic processing, formulation, filtration, mixing, filling, and dispensing
• Work within Moderna’s human performance model for error prevention, carrying out tasks with focus and accountability for accurate execution
• Complete documentation in real time using good documentation practices and data integrity standards
• Maintain the cleanliness, control, and readiness of the production area
• Use manufacturing systems and equipment such as SAP, Veeva, DeltaV, Syncade, LIMS, and CMMS as required
• Build a practical understanding of the equipment, process flow, and digital systems that support manufacturing so you can recognize issues, respond appropriately, and continue to develop and execute technical judgment
• Follow all safety procedures, waste handling requirements, and environmental guidelines
• Complete required training on time and maintain qualifications as needed for gowning and assigned operations
• Work closely with teammates and cross‑functional partners, communicate clearly, escape issues early, and help support smooth execution across the operation

Skills

Strong attention to detail

Disciplined execution

Stay focused

Team‑first mindset

Learn technical processes

Judgment & accountability

Cleanroom comfort

Continuous improvement

Escalate issues early

Education

Bachelor’s degree in STEM

Associate’s degree + 2–4 years

High school diploma + >4 years

Tools

SAP

Veeva

DeltaV

Syncade

LIMS

CMMS

Job description

Moderna is seeking a hands‑on Manufacturing Associate I in Drug Substance Operations to join a highly controlled GMP environment. You will perform aseptic processing, operate with precision, and ensure data integrity while supporting multi‑step production processes for mRNA drug substance.

The role emphasizes adherence to safety, training, and continuous improvement, with a strong focus on teamwork and high‑quality output that directly impacts patient care.