Senior Quality Control Specialist: Cell Therapy

CELULARITY LLC; Florham Park (NJ); On-site; USD 110,000 - 150,000; Full time

Job summary

Celularity Inc. in Florham Park, NJ, is seeking a Sr. Specialist, Quality Control, to support routine product testing for clinical and commercial products, including microbiological activities and assay management.

The role requires interfacing with multiple groups, performing tasks independently, interpreting results, and serving as QC SME during audits when needed. Candidates should have a Bachelor's degree in a scientific discipline and at least 5 years of quality control experience in a cGMP

Qualifications

• Bachelor’s degree in a scientific discipline is required.
• Minimum of 5+ years of quality control and/or analytical experience in a cGMP-regulated environment.
• Understanding and application of good laboratory practices.
• Strong organizational and time management skills.
• Ability to work well in a team and communicate effectively.
• Independent, self-starting, and adaptable.
• Excellent attention to detail and PPE as required.

Responsibilities

• Perform routine testing of cellular, tissue, in-process and final product samples.
• Record results in controlled documents and electronic systems.
• Assist with assay troubleshooting, calibration, and maintenance.
• Support disposition activities and product release readiness.
• Generate Certificates of Analysis and coordinate testing with QA.
• Participate in internal audits and regulatory inspections.

Skills

Quality control

Analytical testing

cGMP compliance

Documentation & record-keeping

Team collaboration

Time management

Communication skills

Independent work

Adaptability

PPE compliance

Education

Bachelor's degree in a scientific discipline

Job description

Celularity Inc. in Florham Park, NJ, is seeking a Sr. Specialist, Quality Control, to support routine product testing for clinical and commercial products, including microbiological activities and assay management.

The role requires interfacing with multiple groups, performing tasks independently, interpreting results, and serving as QC SME during audits when needed. Candidates should have a Bachelor's degree in a scientific discipline and at least 5 years of quality control experience in a cGMP