Specialist III, QA Operations (Contract)

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  "last_changed_at": "2026-05-29T06:54:38.341Z",
  "active_status": "active"
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  "language": "en",
  "location": {
    "raw": "Redwood City, CA",
    "city": "Redwood City",
    "region": "CA",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.9
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  "salary_max": 60,
  "salary_min": 50,
  "inferred_at": "2026-06-06T20:16:34.286Z",
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    "language": "en",
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      "raw": "Redwood City, CA",
      "city": "Redwood City",
      "region": "CA",
      "country": "United States",
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    "countries": [
      "United States"
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  "remote_policy": null,
  "salary_period": "hour",
  "workplace_type": "on_site",
  "salary_currency": "USD"
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{
  "lists": [
    {
      "text": "What You'll Do:",
      "content": "<div>\n<div>\n<p><strong><span data-contrast=\"auto\">Lot Disposition Oversight:</span></strong></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Review, evaluate, and approve all batch records, analytical testing data, and supporting quality documentation prior&nbsp;to lot&nbsp;release.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Ensure all manufacturing and testing activities are performed in compliance with cGMP and applicable regulatory requirements.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Oversee&nbsp;lot&nbsp;disposition processes for materials produced internally and by CMOs.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><strong><span data-contrast=\"auto\">Data Review and Approval: </span><span data-ccp-props=\"{}\">&nbsp;</span></strong></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Review and assess data generated by CMOs, including in-process and release testing results.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Evaluate data generated by CTLs and in-house testing to verify compliance with specifications and regulatory expectations.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Confirm resolution of deviations, investigations, and change controls prior to lot disposition.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Review stability data, including test records, interim reports, and final stability reports, for accuracy, completeness and compliance </span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><strong><span data-contrast=\"auto\">Compliance and Continuous Improvement:</span><span data-ccp-props=\"{}\">&nbsp;</span></strong></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Ensure&nbsp;timely&nbsp;completion of lot disposition activities to meet clinical and commercial supply timelines.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">-&nbsp;Identify&nbsp;process gaps and drive continuous improvement initiatives in quality systems related to lot disposition.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Support internal and external audits related to lot disposition processes.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><strong><span data-contrast=\"auto\">Cross-Functional Collaboration: </span><span data-ccp-props=\"{}\">&nbsp;</span></strong></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Partner with Manufacturing, QC, Supply Chain, and Regulatory Affairs and Process and Assay Development as&nbsp;required&nbsp;to address quality issues&nbsp;impacting&nbsp;lot disposition.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Provide guidance to internal and external stakeholders on quality standards and regulatory compliance.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n</div>"
    },
    {
      "text": "About You:",
      "content": "<div>\n<div>\n<p><span data-contrast=\"auto\">- Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Pharmacy) or equivalent experience.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Minimum 5&nbsp;years of experience in Quality Assurance within the pharmaceutical, biotechnology, or related regulated industry, including experience with lot disposition.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Experience working with CMOs and CTLs in a&nbsp;cGMP environment preferred.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n<div>\n<p><span data-contrast=\"auto\">- Strong understanding of cGMP, ICH guidelines, and applicable regulatory requirements.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Proficient in reviewing manufacturing batch records, analytical data, and quality documentation.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Excellent attention to detail and&nbsp;ability&nbsp;to make sound quality decisions.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Strong organizational, problem-solving, and communication skills.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">- Ability to work independently and in a cross-functional team environment.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">-&nbsp;Proficiency&nbsp;with electronic quality management systems (e.g.,&nbsp;MasterControl) is a</span><span data-contrast=\"auto\">n asset.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n</div>\n</div>"
    }
  ],
  "country": "US",
  "createdAt": 1775234987248,
  "updatedAt": null,
  "categories": {
    "team": "Quality Assurance",
    "location": "Redwood City, CA",
    "commitment": "Contract",
    "department": "Research & Development",
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      "Redwood City, CA"
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