Process Equipment Engineer II — GMP Manufacturing

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

Benefits offered by this job

Competitive healthcare

Holistic well-being resources

Generous paid time off

Job summary

Moderna Therapeutics in Norwood, MA, is seeking an Engineer II to support process equipment across UF, chromatography, formulations, CIP, and fill lines. You will troubleshoot, optimize, and lead small projects within a GMP manufacturing setting, coordinating with MS&T, Facilities, Validation, and end users.

This role emphasizes reliability, data integrity, and safe implementation of new technologies. You will work 100% onsite and contribute to continuous improvement, documentation, and

Qualifications

• BS or MS in Chemical or Mechanical Engineering or equivalent.
• Minimum 3 years relevant experience in Facilities, Engineering, or Operations.
• Experience in a GxP environment preferred.
• Must be able to investigate issues using structured problem-solving to find root causes and implement CAPAs.

Responsibilities

• Provide direct engineering support for process equipment at Norwood, including UF, chromatography, mixers, CIP, aseptic lines, and more.
• Reduce events and excursions by ensuring optimal functionality of equipment.
• Own small to medium projects with timelines and manager support.
• Participate in design, procurement, installation, startup, validation, and qualification of facilities/equipment.
• Troubleshoot faults, drive root-cause analysis, and implement corrective actions.
• Maintain asset records in CMMS and manage change controls and deviations.

Skills

Analytical skills

Problem solving

Interpersonal communication

Technical writing

Time management

Education

BS or MS in Chemical or Mechanical Engineering

Tools

CMMS

Microsoft Office

Job description

Moderna Therapeutics in Norwood, MA, is seeking an Engineer II to support process equipment across UF, chromatography, formulations, CIP, and fill lines. You will troubleshoot, optimize, and lead small projects within a GMP manufacturing setting, coordinating with MS&T, Facilities, Validation, and end users.

This role emphasizes reliability, data integrity, and safe implementation of new technologies. You will work 100% onsite and contribute to continuous improvement, documentation, and