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Quality Control Associate III, Sample Management

Job in San Diego, San Diego County, California, 92189, USA
Listing for: Capricor Therapeutics, Inc.
Full Time position
Listed on 2026-06-04
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
Salary/Wage Range or Industry Benchmark: 75000 - 95000 USD Yearly USD 75000.00 95000.00 YEAR
Job Description & How to Apply Below

The Quality Control Associate III, Sample Management is responsible for the receipt, tracking, storage, distribution, and disposal of samples in a controlled laboratory or regulated environment. This role ensures sample integrity, accurate documentation, and compliance with applicable regulatory and quality standards.

Responsibilities
  • Receive, log, label, and track incoming samples using a laboratory information management system (LIMS) or equivalent tracking system
  • Verify sample documentation for accuracy, completeness, and compliance with protocols
  • Maintain proper storage conditions (e.g., temperature‑controlled environments such as refrigerators, freezers, and ambient storage)
  • Monitor and document storage conditions, including temperature logs and alarm responses
  • Coordinate sample distribution (i.e., in‑house, release, and stability) to internal departments or external laboratories
  • Ensure chain‑of‑custody documentation is accurate and maintained
  • Perform inventory management, including reconciliation and periodic audits
  • Dispose of samples according to safety, regulatory, and company procedures
  • Investigate and document sample discrepancies, deviations, or nonconformances
  • Support laboratory operations by preparing materials as needed
  • Maintain clean, organized, and compliant storage areas
Required Qualifications (Must‑Haves)
  • Bachelor’s degree in Biology, Chemistry, Microbiology, or a related scientific field (or equivalent experience)
  • 3–5 years of experience in a laboratory, sample management, or regulated environment
  • Familiarity with LIMS or electronic tracking systems
  • Knowledge of GMP/GLP regulations
Skills and Competencies
  • Strong attention to detail and organizational skills
  • Ability to manage multiple priorities and meet deadlines
  • Good documentation practices (GDP) knowledge
  • Strong communication and teamwork skills
  • Problem‑solving and critical thinking abilities
Work Environment &

Physical Requirements
  • Ability to sit or stand for extended periods and move throughout the facility
  • Ability to gown and enter classified areas when required
  • Ability to lift and carry up to 40 lbs as needed

$75,000 - $95,000 a year

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Position Requirements
10+ Years work experience
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