{"schemaVersion":"jobsearcher.job.v1","id":"4b979cb0a9fd7ef6dca2182c","url":"https://jobsearcher.com/jobs/4b979cb0a9fd7ef6dca2182c","canonicalUrl":"https://jobsearcher.com/jobs/4b979cb0a9fd7ef6dca2182c","title":"Quality Manager","description":"Description: Job: Senior Manager\nR&D Deviation and CAPA Management\nR&D Quality and Medical Governance\nOnsite - T/W/Th\nLocation - Parsippany, NJ (preferred) or Foster City, CA\nPrimary Responsibilities\nLead and facilitate Quality Event Investigations and subsequent CAPA development in accordance with defined timelines and in collaboration with appropriate subject matter experts\nBuild, deploy and reinforce learning tools and materials to support quality event management capability development\nOversee the standard and timeliness of deviation and CAPA completion\nWork with the business process owners to identify issues and improvement requirements and lead those improvement initiatives\nIn support of the quality management system module leads maintain records of issues, enhancement requests and support the implementation of system changes\nAdminister notification to management and escalation process\nParticipate in risk assessments and act as risk facilitator\nCandidate Requirements\nGxP experience is preferred\n10+ years experience in Biopharma experience\n6+ years managing investigations (deviations, CAPA, etc)\nExperience writing investigations\nExperience managing RCA\nJob Type: Contract\nPay: $70.00 - $75.00 per hour\nExpected hours: 40 per week\nBenefits:\n401(k)\n401(k) matching\nDental insurance\nHealth insurance\nLife insurance\nPaid time off\nVision insurance\nSchedule:\n8 hour shift\nMonday to Friday\nApplication Question(s):\nDo you have experience with Quality Event Investigations and subsequent CAPA development? If yes, Mention Client Name?\nAre you comfortable with Rate $75/hr on W2?\nAre you comfortable with onsite in Foster City CA?\nExperience:\nCAPA: 8 years (Required)\nR&D Deviation: 6 years (Required)\nWork Location: On the road","company":"Indominds Solutions","rawCompany":"indominds solutions","city":"Millbrae","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-08-04T14:23:05.911Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-9199.02","title":"Compliance Managers","slug":"compliance-managers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Quality Manager","description":"Description: Job: Senior Manager\nR&D Deviation and CAPA Management\nR&D Quality and Medical Governance\nOnsite - T/W/Th\nLocation - Parsippany, NJ (preferred) or Foster City, CA\nPrimary Responsibilities\nLead and facilitate Quality Event Investigations and subsequent CAPA development in accordance with defined timelines and in collaboration with appropriate subject matter experts\nBuild, deploy and reinforce learning tools and materials to support quality event management capability development\nOversee the standard and timeliness of deviation and CAPA completion\nWork with the business process owners to identify issues and improvement requirements and lead those improvement initiatives\nIn support of the quality management system module leads maintain records of issues, enhancement requests and support the implementation of system changes\nAdminister notification to management and escalation process\nParticipate in risk assessments and act as risk facilitator\nCandidate Requirements\nGxP experience is preferred\n10+ years experience in Biopharma experience\n6+ years managing investigations (deviations, CAPA, etc)\nExperience writing investigations\nExperience managing RCA\nJob Type: Contract\nPay: $70.00 - $75.00 per hour\nExpected hours: 40 per week\nBenefits:\n401(k)\n401(k) matching\nDental insurance\nHealth insurance\nLife insurance\nPaid time off\nVision insurance\nSchedule:\n8 hour shift\nMonday to Friday\nApplication Question(s):\nDo you have experience with Quality Event Investigations and subsequent CAPA development? If yes, Mention Client Name?\nAre you comfortable with Rate $75/hr on W2?\nAre you comfortable with onsite in Foster City CA?\nExperience:\nCAPA: 8 years (Required)\nR&D Deviation: 6 years (Required)\nWork Location: On the road","datePosted":"2026-08-04T14:23:05.911Z","dateModified":"2026-08-04T14:23:05.911Z","hiringOrganization":{"@type":"Organization","name":"Indominds Solutions","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Millbrae","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"4b979cb0a9fd7ef6dca2182c"},"url":"https://jobsearcher.com/jobs/4b979cb0a9fd7ef6dca2182c"}}