Senior QC Specialist - Cell Therapy & GMP Analytics

Energy Jobline ZR

Florham Park (NJ)

On-site

USD 90,000 - 130,000

Full time

5 days ago
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Job summary

Celularity Inc. is seeking a Sr. Specialist, Quality Control to support routine product testing for clinical and commercial products, visual inspection, retain/sample oversight, microbiological activities and assay management.

This role interfaces with multiple groups, performs tasks independently, and may act as QC SME during audits. Responsibilities include generating COAs, investigating deviations, maintaining sample management, and supporting equipment calibration and method transfers in a

Qualifications

  • Bachelor’s degree in a scientific discipline required.
  • Minimum of 5+ years of quality control and/or analytical experience in a cGMP-regulated environment.
  • Ability to understand, follow, interpret and apply good laboratory practices.
  • Strong organizational and time management skills.
  • Ability to work well in a team environment.
  • Independent and self-starting with good communication.

Responsibilities

  • Perform routine testing of cellular, tissue, in-process and final product samples.
  • Record testing activities and results in controlled documents and/or electronic systems.
  • Support investigations associated with deviations and OOS/OOT results.
  • Coordinate and execute testing and inspection of incoming materials.
  • Prepare samples for testing and shipment to external labs.
  • Participate in internal audits and regulatory inspections.

Skills

Quality control
Analytical testing
Documentation
Team collaboration
Communication
Independent and self-starting
Adaptable
PPE compliance

Education

Bachelor’s degree in a scientific discipline

Job description

Celularity Inc. is seeking a Sr. Specialist, Quality Control to support routine product testing for clinical and commercial products, visual inspection, retain/sample oversight, microbiological activities and assay management.

This role interfaces with multiple groups, performs tasks independently, and may act as QC SME during audits. Responsibilities include generating COAs, investigating deviations, maintaining sample management, and supporting equipment calibration and method transfers in a

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