Lead Maintenance Engineer, Aseptic & GMP Reliability

RXinsider LTD.

Norwood, Northern (MA, KY)

Hybrid

USD 90,000 - 144,000

Full time

9 days ago
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Benefits offered by this job

Healthcare benefits
Well-being resources
Family planning benefits
Paid time off
Savings and investments
Location-based perks

Job summary

Moderna is seeking a Sr. Specialist, Maintenance to lead maintenance, troubleshoot, and ensure reliability of GMP and non-GMP process equipment, with emphasis on aseptic filling systems and high-precision pharmaceutical machinery.

You will act as technical lead, support commissioning/startup activities, and drive continuous improvement across manufacturing systems, while maintaining cGMP documentation and coordinating with cross-functional teams.

Qualifications

  • AS degree or certificate in a science/technical field or a technical trade school.
  • 9+ years of experience in maintenance/reliability roles.
  • Experience in GMP environments and aseptic systems is highly desirable.

Responsibilities

  • Perform advanced preventative and corrective maintenance on process and utility systems in GMP environments.
  • Lead troubleshooting and repair of complex mechanical and electromechanical systems.
  • Act as primary responder to equipment issues and ensure full resolution.
  • Support asset management and reliability initiatives.
  • Maintain aseptic filling machines, perform setup/changeovers, and tune performance.
  • Lead commissioning, FAT/SAT, and startup activities.
  • Maintain accurate cGMP documentation and SOPs.

Skills

Preventative maintenance
Troubleshooting
GMP compliance
Aseptic filling systems
Asset management
Leadership

Education

AS degree or certificate in a science/technical field or a technical trade school

Job description

Moderna is seeking a Sr. Specialist, Maintenance to lead maintenance, troubleshoot, and ensure reliability of GMP and non-GMP process equipment, with emphasis on aseptic filling systems and high-precision pharmaceutical machinery.

You will act as technical lead, support commissioning/startup activities, and drive continuous improvement across manufacturing systems, while maintaining cGMP documentation and coordinating with cross-functional teams.

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