2nd-Shift Biotech Maintenance Tech I/II

BioSpace

Raritan (NJ)

Vor Ort

USD 84.000 - 110.000

Vollzeit

vor 42 Stunden
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

Medical, dental, and vision insurance
401(k) with company match
Paid parental leave

Zusammenfassung

Legend Biotech in New Jersey seeks a Maintenance Tech I/II (2nd Shift) to maintain HVAC, cleanroom systems, and related equipment for cGMP cell therapy manufacturing in a fast-paced environment.

The role requires 8+ years in industrial manufacturing, CMMS experience, and strong English communication. Training and regulatory compliance are essential for this technically demanding position in the Facilities and Engineering team.

Qualifikationen

  • B.Sc./M.Sc. in Biological/Biochemical Science/Bioengineering or minimum high school diploma with equivalent experience.
  • Trade/Technical School Certification or Certification in Craft.
  • 8+ years of experience in an industrial manufacturing or regulated environment, ideally with cGMP cleanroom experience under aseptic conditions.
  • Proficiency in CMMS or similar maintenance management system.
  • Proficiency in English (verbal and written) with strong communication skills.

Aufgaben

  • Diagnose, troubleshoot, repair, and maintain HVAC, clean room HVAC, refrigeration, clean steam, cryogenic storage, and process equipment and systems.
  • Perform minor upgrades and installations of facilities and systems.
  • Support maintenance-driven quality events and regulatory/quality investigations.
  • Read and interpret blueprints, P&IDs, and drawings; maintain GDP documentation on the CMMS.
  • Possess ability to manage shifting priorities and work with minimal supervision.

Kenntnisse

HVAC systems
Troubleshooting
Mechanical maintenance
P&IDs / drawings

Ausbildung

B.Sc./M.Sc. in Biological/Biochemical Science/Bioengineering or HS diploma with experience

Tools

CMMS

Jobbeschreibung

Legend Biotech in New Jersey seeks a Maintenance Tech I/II (2nd Shift) to maintain HVAC, cleanroom systems, and related equipment for cGMP cell therapy manufacturing in a fast-paced environment.

The role requires 8+ years in industrial manufacturing, CMMS experience, and strong English communication. Training and regulatory compliance are essential for this technically demanding position in the Facilities and Engineering team.

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