Process Engineer II: GMP Equipment & CI

Initial Therapeutics, Inc.

Norwood (MA)

On-site

USD 74,000 - 118,000

Full time

10 days ago
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Benefits offered by this job

Competitive healthcare benefits
Well-being resources
Paid time off and sabbatical options
Family planning support
Bonuses and equity potential

Job summary

Moderna is seeking an Engineer II to lead and optimize manufacturing equipment at the Norwood, MA site. You will troubleshoot, support capital projects, and drive improvements across chromatography, filtration and fill/finish lines.

The role focuses on reducing events, improving product quality, and ensuring regulatory compliance with SOPs and GMP guidelines. This is a 100% onsite opportunity requiring collaboration with MS&T, Facilities, and QA teams.

Qualifications

  • BS or MS in Chemical or Mechanical Engineering (or equivalent).
  • Minimum 3 years in Facilities, Engineering, or Operations.
  • None mentioned for certifications.

Responsibilities

  • Provide direct engineering support for process equipment at Norwood, MA.
  • Reduce manufacturing events and batch excursions through optimal equipment function.
  • Own small to medium projects with strong timelines and managerial support.
  • Participate in design, procure, install, start-up, validation and qualification of facilities/equipment.
  • Troubleshoot, determine root cause, implement corrective actions and change controls.
  • Maintain process equipment assets in CMMS and manage quality records.

Skills

Analytical skills
Problem solving
Cross functional collaboration
Attention to detail

Education

BS/MS in Chemical Engineering or Mechanical Engineering

Tools

CMMS
Microsoft Office

Job description

Moderna is seeking an Engineer II to lead and optimize manufacturing equipment at the Norwood, MA site. You will troubleshoot, support capital projects, and drive improvements across chromatography, filtration and fill/finish lines.

The role focuses on reducing events, improving product quality, and ensuring regulatory compliance with SOPs and GMP guidelines. This is a 100% onsite opportunity requiring collaboration with MS&T, Facilities, and QA teams.

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