Process Engineer II - Aseptic Filling & Packaging

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

Benefits offered by this job

Competitive healthcare

Well-being resources

Family planning benefits

Generous PTO

Savings & investments

Location-specific perks

Job summary

Moderna is seeking a Process Engineer II to support aseptic filling, visual inspection, and secondary packaging at the Norwood, MA site. You will troubleshoot equipment, support investigations, and drive continuous improvement in a GMP manufacturing environment.

You will collaborate with Manufacturing, Quality, MS&T, Validation, Automation, and Facilities to optimize reliability, contribute to qualification activities, and manage lifecycle documentation.

Qualifications

• Bachelor's degree in Mechanical/Chemical/Biomedical Engineering or related field.
• Typically 2–5 years of GMP pharmaceutical manufacturing, process engineering, or equipment engineering experience.
• Experience supporting manufacturing equipment in regulated environments.
• Strong troubleshooting and analytical problem-solving skills.
• Ability to work effectively in a fast-paced, cross-functional environment.

Responsibilities

• Provide on-floor engineering support during manufacturing operations.
• Troubleshoot equipment and process issues and support investigations.
• Participate in CAPAs and root cause analysis.
• Support commissioning, IQ/OQ/PQ, and equipment validation activities.
• Coordinate vendor activities and maintain engineering documentation.

Skills

Troubleshooting

Analytical problem-solving

Cross-functional collaboration

Effective communication

Excel

Data analysis

Education

Bachelor's degree in Mechanical Engineering, Chemical Engineering, Biomedical Engineering, or related engineering discipline

Tools

Maximo CMMS

Electronic batch records

Job description

Moderna is seeking a Process Engineer II to support aseptic filling, visual inspection, and secondary packaging at the Norwood, MA site. You will troubleshoot equipment, support investigations, and drive continuous improvement in a GMP manufacturing environment.

You will collaborate with Manufacturing, Quality, MS&T, Validation, Automation, and Facilities to optimize reliability, contribute to qualification activities, and manage lifecycle documentation.