On-Site QC Sample Coordinator — Lab Data & Compliance

MSCCN

Harvard (MA)

On-site

USD 50,000 - 61,000

Full time

6 days ago
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Job summary

Bristol Myers Squibb in Devens, MA is seeking a QC Sample Management Technician to oversee movement and control of QC samples, including in-process, finished product, and stability samples. The role supports GMP documentation, data review, and continuous improvement within a 12‑hour rotating shift.

The position requires a Bachelor's degree in science, 2+ years of LIMS/QC experience, and strong attention to regulatory compliance. On-site work with potential overtime and weekend work is expected.

Qualifications

  • Bachelor's degree or equivalent required, preferably in science.
  • 2+ years of relevant LIMS or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
  • Demonstrated experience in LIMS and knowledge of Chain of Identity and Chain of Custody.

Responsibilities

  • Perform routine management of in-process, final product and stability samples and QC data throughout the sample lifecycle from receipt to disposition.
  • Performs data compilation and review of GMP documentation in support of method trending.
  • Compiles lot files for QC disposition review. Generate SOTR and manual CoA.
  • Support document revision, project, CAPA and deviation investigation related tasks and/ or continuous improvement efforts.
  • Train analysts on general job duties.
  • Perform other tasks/duties as assigned.

Skills

Regulatory knowledge
cGMP
LIMS
ELN
Data analysis
Documentation
Communication
Teamwork

Education

Bachelor's degree in science

Tools

LIMS
ELN

Job description

Bristol Myers Squibb in Devens, MA is seeking a QC Sample Management Technician to oversee movement and control of QC samples, including in-process, finished product, and stability samples. The role supports GMP documentation, data review, and continuous improvement within a 12‑hour rotating shift.

The position requires a Bachelor's degree in science, 2+ years of LIMS/QC experience, and strong attention to regulatory compliance. On-site work with potential overtime and weekend work is expected.

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