Quality Control Associate II, Controls

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  "source_hash": "58f029d7016cb04de458f1d950c24f69534bfea54e83c53ac3418e5466172433",
  "last_changed_at": "2026-05-29T07:08:24.772Z",
  "active_status": "active"
}

{
  "language": "en",
  "location": {
    "raw": "San Diego, CA",
    "city": "San Diego",
    "region": "CA",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.9
  },
  "salary_max": 87000,
  "salary_min": 75000,
  "inferred_at": "2026-06-06T19:46:29.791Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "San Diego, CA",
      "city": "San Diego",
      "region": "CA",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.9
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": "year",
  "workplace_type": "on_site",
  "salary_currency": "USD"
}

{}

{
  "lists": [
    {
      "text": "Responsibilities",
      "content": "<div>\n<div>\n\n<li><span data-contrast=\"auto\">Generate, prepare, and&nbsp;maintain&nbsp;positive and negative control materials used in QC analytical assays.</span></li>\n<li><span data-contrast=\"auto\">Support the qualification and characterization of control materials to ensure suitability for routine QC testing.</span></li>\n<li><span data-contrast=\"auto\">Execute analytical assays to support control evaluation, assay troubleshooting, and assay optimization studies.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n<li><span data-contrast=\"auto\">Perform laboratory activities related to control generation, characterization, and assay performance evaluation.</span></li>\n<li><span data-contrast=\"auto\">Maintain inventory, traceability, and documentation of assay control materials used across QC testing programs.</span></li>\n<li><span data-contrast=\"auto\">Analyze experimental data, summarize results, and document findings in accordance with GMP and data integrity requirements.</span></li>\n<li><span data-contrast=\"auto\">Document all laboratory work in GMP-compliant systems including laboratory notebooks, controlled forms, and electronic records.</span></li>\n<li><span data-contrast=\"auto\">Support preparation and maintenance of technical documentation including study protocols, reports, SOP updates, and control qualification records.</span></li>\n<li><span data-contrast=\"auto\">Assist with investigations related to assay performance including deviations, OOS/OOT events, and atypical assay results.</span></li>\n<li><span data-contrast=\"auto\">Collaborate with QC scientists and cross-functional teams including Analytical Development, Process Development, Manufacturing, and Quality to support assay readiness and continuous improvement initiatives.</span></li>\n<li><span data-contrast=\"auto\">Manage multiple laboratory assignments and testing priorities to meet project timelines and QC operational needs.</span></li>\n<li><span data-contrast=\"auto\">Perform additional QC duties as assigned.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n\n</div>\n</div>"
    },
    {
      "text": "Required Qualifications (Must‑Haves)",
      "content": "<div>\n<div>\n\n<li><span data-contrast=\"auto\">Bachelor’s degree in Biological Sciences, Biochemistry, Molecular Biology, or&nbsp;a related&nbsp;discipline.</span></li>\n<li><span data-contrast=\"auto\">2+ years of laboratory experience in biotechnology, pharmaceutical, or GMP-regulated environments.</span></li>\n<li><span data-contrast=\"auto\">Hands-on experience performing analytical assays such as ELISA, PCR/qPCR, flow cytometry, or other biochemical or cell-based assays.</span></li>\n<li><span data-contrast=\"auto\">Experience preparing or maintaining assay controls or reference materials.</span></li>\n<li><span data-contrast=\"auto\">Strong laboratory documentation practices and familiarity with GMP and data integrity expectations.</span></li>\n<li><span data-contrast=\"auto\">Ability to analyze data and communicate findings clearly.</span></li>\n<li><span data-contrast=\"auto\">Ability to work independently and manage multiple assignments in a laboratory environment.</span></li>\n<li><span data-contrast=\"auto\">Strong organizational and time management skills.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n\n</div>\n</div>"
    },
    {
      "text": "Preferred Qualifications (Nice‑to‑Haves)",
      "content": "<div>\n<div>\n\n<li><span data-contrast=\"auto\">Experience supporting analytical studies related to assay performance or assay optimization.</span></li>\n<li><span data-contrast=\"auto\">Experience working with mammalian cell culture or cell-based assays.</span></li>\n<li><span data-contrast=\"auto\">Experience supporting method qualification or assay performance monitoring activities.</span></li>\n<li><span data-contrast=\"auto\">Experience supporting deviations, investigations, or technical reports in regulated environments.</span></li>\n<li><span data-contrast=\"auto\">Experience working with cell therapy, biologics, or exosome-based products.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n\n</div>\n</div>"
    },
    {
      "text": "Work Environment & Physical Requirements",
      "content": "<div>\n<div>\n\n<li><span data-contrast=\"auto\">Laboratory-based role&nbsp;requiring&nbsp;routine bench work.</span></li>\n<li><span data-contrast=\"auto\">Work involves analytical instrumentation, laboratory documentation, and computer-based data analysis.</span></li>\n<li><span data-contrast=\"auto\">Ability to lift up to 20 pounds.</span></li>\n<li><span data-contrast=\"auto\">Occasional participation in cross-functional meetings and technical discussions.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n\n</div>\n</div>"
    }
  ],
  "country": "US",
  "createdAt": 1779486723320,
  "updatedAt": null,
  "categories": {
    "team": "Quality Control",
    "location": "San Diego, CA",
    "commitment": "Full-time (exempt)",
    "department": "Capricor Therapeutics",
    "allLocations": [
      "San Diego, CA"
    ]
  },
  "salaryRange": {
    "max": 87000,
    "min": 75000,
    "currency": "USD",
    "interval": "per-year-salary"
  },
  "workplaceType": "onsite"
}