Quality Control Scientist, Controls

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  "last_changed_at": "2026-05-29T07:08:24.772Z",
  "active_status": "active"
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{
  "language": "en",
  "location": {
    "raw": "San Diego, CA",
    "city": "San Diego",
    "region": "CA",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.9
  },
  "salary_max": 115000,
  "salary_min": 95000,
  "inferred_at": "2026-06-06T19:46:29.797Z",
  "launch_scope": {
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    "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"
    ]
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  "remote_policy": null,
  "salary_period": "year",
  "workplace_type": "on_site",
  "salary_currency": "USD"
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{}

{
  "lists": [
    {
      "text": "Responsibilities",
      "content": "<div>\n<div>\n\n<li><span data-contrast=\"auto\">Lead the development, qualification, and maintenance of positive and negative control materials used in QC analytical assays.</span></li>\n<li><span data-contrast=\"auto\">Establish and oversee assay control strategies to ensure reliable assay performance and consistency across QC testing programs.</span></li>\n<li><span data-contrast=\"auto\">Serve as the scientific owner for control materials within the analytical lifecycle framework, including control generation, qualification, monitoring, and lifecycle management.</span></li>\n<li><span data-contrast=\"auto\">Design and execute analytical studies to evaluate assay performance, control suitability, assay robustness, and method reliability.</span></li>\n<li><span data-contrast=\"auto\">Provide scientific leadership for assay troubleshooting and optimization activities to improve assay robustness and reproducibility.</span></li>\n<li><span data-contrast=\"auto\">Evaluate assay performance trends and control performance data to identify opportunities for improving assay reliability.</span></li>\n<li><span data-contrast=\"auto\">Analyze experimental data, interpret results, and generate scientific reports, study summaries, and technical documentation.</span></li>\n<li><span data-contrast=\"auto\">Document experimental work and study outcomes in accordance with GMP and data integrity requirements.</span></li>\n<li><span data-contrast=\"auto\">Support preparation and maintenance of technical documentation including study protocols, reports, SOP updates, control qualification records, and analytical lifecycle documentation.</span></li>\n<li><span data-contrast=\"auto\">Support regulatory inspection readiness by ensuring analytical control strategies, documentation, and study records meet regulatory expectations.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n<li><span data-contrast=\"auto\">Provide scientific support for investigations including deviations, OOS/OOT events, and assay performance issues.</span></li>\n<li><span data-contrast=\"auto\">Collaborate with Analytical Development, Process Development, Manufacturing, and Quality teams to support assay lifecycle management and continuous improvement initiatives.</span></li>\n<li><span data-contrast=\"auto\">Manage multiple scientific projects and timelines to support QC laboratory priorities.</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\n<li><span data-contrast=\"auto\">Ph.D. in Biological Sciences, Biochemistry, Molecular Biology, Bioengineering, or&nbsp;a related&nbsp;discipline.</span></li>\n<li><span data-contrast=\"auto\">Strong background in primary cell culture and analytical assay development, troubleshooting, and experimental design.</span></li>\n<li><span data-contrast=\"auto\">Hands-on experience with analytical techniques such as ELISA, PCR/qPCR, flow cytometry, or other biochemical or cell-based assays.</span></li>\n<li><span data-contrast=\"auto\">Experience designing and executing analytical studies and interpreting experimental data.</span></li>\n<li><span data-contrast=\"auto\">Strong understanding of assay controls, assay performance monitoring, and analytical method lifecycle management.</span></li>\n<li><span data-contrast=\"auto\">Strong written and verbal communication skills with the ability to clearly summarize complex scientific findings.</span></li>\n<li><span data-contrast=\"auto\">Ability to work independently and manage multiple scientific projects in a fast-paced environment.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n\n</div>"
    },
    {
      "text": "Preferred Qualifications (Nice‑to‑Haves)",
      "content": "<div>\n<div>\n\n<li><span data-contrast=\"auto\">Experience working in GMP or regulated laboratory environments.</span></li>\n<li><span data-contrast=\"auto\">Experience supporting analytical method qualification, validation, or lifecycle management.</span></li>\n<li><span data-contrast=\"auto\">Experience working with cell-based assays or mammalian cell culture systems.</span></li>\n<li><span data-contrast=\"auto\">Experience supporting deviations, assay investigations, or technical reports in regulated environments.</span></li>\n<li><span data-contrast=\"auto\">Experience 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": 1779486493609,
  "updatedAt": null,
  "categories": {
    "team": "Quality Control",
    "location": "San Diego, CA",
    "commitment": "Full-time (exempt)",
    "department": "Capricor Therapeutics",
    "allLocations": [
      "San Diego, CA"
    ]
  },
  "salaryRange": {
    "max": 115000,
    "min": 95000,
    "currency": "USD",
    "interval": "per-year-salary"
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  "workplaceType": "onsite"
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