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1–2 jobs· newest first

Senior Specialist, QC Analytical, Cell TherapyNew
Bristol Myers Squibb · US
$41–$50Full-time · Senior
Specialist, QC Analytical Cell Therapy - Summit West NJ
VetJobs · Summit West, US
$35–$42On-site

+10K new in the last hour

Senior Specialist, QC Analytical, Cell Therapy

Bristol Myers Squibb · Posted Nov 10, 2026

New Jersey, United States
Full-time · Senior
$41–$50 per hour

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Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification. Perform method troubleshooting, training, and transfer/validation. Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts.

Compensation

Summit West - NJ - US: $40.97 - $49.64per hour

Responsibilities

Perform method transfer/validation and routine testing of in-process, final product, and stability samples.
Anticipate and perform routine troubleshooting and problem solving with minimal guidance.
Perform data verification, data review and review of GMP documentation for general and complex methods.
Perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
Train and mentor others on QC test methods, processes and procedures.

Requirements

Nice to have: advanced knowledge of LIMS
Nice to have: advanced knowledge of ELN

Skills

LIMS ELN laboratory data analysis systems method transfer validation QC testing data verification GMP documentation CAPA deviation troubleshooting training mentoring

Benefits

comprehensive benefit plans
flexible time off
paid vacation
sick leave
volunteer days

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Specialist, QC Analytical Cell Therapy - Summit West NJ

VetJobs · Posted Nov 5, 2026

Summit West, New Jersey, United States
On-site
$35–$42 per hour
2+ years

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Responsible for supporting QC testing for in-process, final product, and stability samples, including data review/verification.

Compensation

Summit West - NJ - US: $34.82 - $42.19per hour Field - United States - US: $134,390 - $162,843

Responsibilities

Perform routine testing of in-process, final product, and stability samples.
Perform testing for method transfer/validation/verification.
Perform data verification, data review and review of GMP documentation for general methods.
May perform document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
Train analysts on general job duties.

Requirements

Bachelor's degree or equivalent required, preferably in science.
Nice to have: writing technical documents

Skills

LIMS ELN laboratory data analysis systems cell and molecular biology techniques flow cytometry

aseptic technique

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