Senior Engineering Manager, Cell Therapy Manufacturing

Socket.dev

Raritan (NJ)

On-site

USD 146,000 - 192,000

Full time

14 days+
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Benefits offered by this job

Medical insurance
401(k) matching
Paid parental leave

Job summary

Legend Biotech, based in New Jersey, seeks a Senior Manager, Engineering to lead a multidisciplinary team supporting CAR-T cell therapy manufacturing operations. You will direct lifecycle management of equipment and process systems, drive continuous improvement, and ensure regulatory compliance across manufacturing processes.

The role requires 10+ years in engineering/manufacturing with 5+ years in people leadership, and strong experience with cGMP, investigations, and CAPA programs.

Qualifications

  • 10+ years of engineering, manufacturing, technical operations, or process support experience in regulated biopharma
  • 5+ years of people leadership managing technical or engineering teams
  • Experience supporting cGMP manufacturing operations
  • Experience leading complex investigations and CAPA implementations

Responsibilities

  • Lead a multidisciplinary engineering organization for cell therapy manufacturing operations.
  • Own lifecycle management strategy for equipment, utilities, and process systems.
  • Drive asset reliability, regulatory compliance, and continuous improvement across manufacturing.
  • Lead the Facilities Investigation Team for non-conformance investigations and CAPA.

Skills

People leadership
Engineering leadership
Data analytics
Cross-functional collaboration
Root cause analysis

Education

Bachelor's degree in Engineering
Master's degree or MBA preferred

Job description

Legend Biotech, based in New Jersey, seeks a Senior Manager, Engineering to lead a multidisciplinary team supporting CAR-T cell therapy manufacturing operations. You will direct lifecycle management of equipment and process systems, drive continuous improvement, and ensure regulatory compliance across manufacturing processes.

The role requires 10+ years in engineering/manufacturing with 5+ years in people leadership, and strong experience with cGMP, investigations, and CAPA programs.

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