C
Capricor18d ago
USD 75000–87000/yr

Quality Control Associate III, Sample Management

United StatesUnited States·San DiegoFull-time (exempt)mid
OtherQuality Control AssociateQuality Control
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Quick Summary

Overview

Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases.

Technical Tools
OtherQuality Control AssociateQuality Control
Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.

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.

  • 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
  • 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 required
  • Familiarity with LIMS or electronic tracking systems
  • Knowledge of GMP/GLP regulations is required
  • 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
  • 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.
  • Location & Eligibility

    Where is the job
    San Diego, United States
    On-site at the office
    Who can apply
    US
    Listed under
    United States

    Listing Details

    Posted
    April 10, 2026
    First seen
    April 10, 2026
    Last seen
    April 28, 2026

    Posting Health

    Days active
    18
    Repost count
    0
    Trust Level
    47%
    Scored at
    April 28, 2026

    Signal breakdown

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    C
    Quality Control Associate III, Sample ManagementUSD 75000–87000