{"schemaVersion":"jobsearcher.job.v1","id":"3ee9e5f96ff95676ea9466f3","url":"https://jobsearcher.com/jobs/3ee9e5f96ff95676ea9466f3","canonicalUrl":"https://jobsearcher.com/jobs/3ee9e5f96ff95676ea9466f3","title":"Quality Associate 2 – Batch Release","description":"Why join Team Singota?\n\nWe pride ourselves on a high-trust, high-accountability environment where we lift each other up. When you join Singota, you are a part of a team that respects, supports, and values its people. We celebrate wins together, brainstorm solutions together, and genuinely enjoy the work we do. The result? A team that’s not just efficient, but also passionate, dedicated, and fun to work with.\n\nJob Title: Quality Associate 2 – Batch Release\n\nDepartment: QA\n\nReports to: Quality Assurance Supervisor\n\nLocation: Bloomington, IN (Onsite)\n\nPosition Type: Full-time, Exempt, 40 hr/wk\n\nGeneral Description:\n\nThe Quality Associate 2 – Batch Release is responsible for managing the workflow of records for Manufacturing and\n\nQC/Development activities in accordance with company, client and regulatory quality standards, including the\n\nappropriate disposition of materials or manufactured product. This position is responsible for reviewing records for\n\naccuracy and completeness and for identifying discrepancies or issues that could result in product impact.\n\n1. Responsible for the issuance, review, and release of batch records and protocols. Ensure records are executed in accordance with procedures and regulatory requirements.\n\n2. Perform disposition of materials within the electronic inventory management system, issue appropriate release documentation.\n\n3. Collaborate with various departments to ensure record specifications are accurate and related deviations are thoroughly investigated.\n\n4. Interface with clients to provide support for review and release of records related to client material or product.\n\n5. Author complex deviations, CAPAs, and change controls as needed.\n\n6. Participate in the training of new Quality Assurance staff.\n\n7. Support continuous improvement of the site’s Quality Systems.\n\n8. Generate and issue controlled labeling material for manufacturing operations. Review for legibility, accuracy, and compliance to company, client, and regulatory standards.\n\n9. Review and disposition Quality Control/Development Laboratory records.\n\n10. Write and review Standard Operating Procedures related to Quality Systems within Manufacturing and QC/Development.\n\n11. Responsible for the development and issuance of Quality operational metrics.\n\n12. Represent Quality Assurance at various project and technical meetings.\n\n13. Must perform other duties as assigned by supervision. Responsible for notifying supervision when issues arise.\n\n14. Comply with quality and safety management systems including requirements for documentation, training, system use, SOPs, processes, and procedures\n\nBenefits\nDental insurance - effective day one of employment\n\nHealth insurance - effective day one of employment\n\nVision insurance - effective day one of employment\n\nHealth savings account\n\nLife & AD&D insurance\n\nShort & long term disability\n\nPaid time off & holidays\n\nEmployee Assistance Program\n\nTuition assistance\n\nSam's Club Basic membership reimbursement\n401(k) with company match\n\nSingota Solutions is an Equal Opportunity Employer","company":"Singota Solutions","rawCompany":"singota solutions","city":"Bloomington","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-08-11T10:44:47.919Z","occupations":[{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"51-9061.00","title":"Inspectors, Testers, Sorters, Samplers, and Weighers","slug":"inspectors-testers-sorters-samplers-and-weighers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"325413","title":"In-Vitro Diagnostic Substance Manufacturing","slug":"in-vitro-diagnostic-substance-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Quality Associate 2 – Batch Release","description":"Why join Team Singota?\n\nWe pride ourselves on a high-trust, high-accountability environment where we lift each other up. When you join Singota, you are a part of a team that respects, supports, and values its people. We celebrate wins together, brainstorm solutions together, and genuinely enjoy the work we do. The result? A team that’s not just efficient, but also passionate, dedicated, and fun to work with.\n\nJob Title: Quality Associate 2 – Batch Release\n\nDepartment: QA\n\nReports to: Quality Assurance Supervisor\n\nLocation: Bloomington, IN (Onsite)\n\nPosition Type: Full-time, Exempt, 40 hr/wk\n\nGeneral Description:\n\nThe Quality Associate 2 – Batch Release is responsible for managing the workflow of records for Manufacturing and\n\nQC/Development activities in accordance with company, client and regulatory quality standards, including the\n\nappropriate disposition of materials or manufactured product. This position is responsible for reviewing records for\n\naccuracy and completeness and for identifying discrepancies or issues that could result in product impact.\n\n1. Responsible for the issuance, review, and release of batch records and protocols. Ensure records are executed in accordance with procedures and regulatory requirements.\n\n2. Perform disposition of materials within the electronic inventory management system, issue appropriate release documentation.\n\n3. Collaborate with various departments to ensure record specifications are accurate and related deviations are thoroughly investigated.\n\n4. Interface with clients to provide support for review and release of records related to client material or product.\n\n5. Author complex deviations, CAPAs, and change controls as needed.\n\n6. Participate in the training of new Quality Assurance staff.\n\n7. Support continuous improvement of the site’s Quality Systems.\n\n8. Generate and issue controlled labeling material for manufacturing operations. Review for legibility, accuracy, and compliance to company, client, and regulatory standards.\n\n9. Review and disposition Quality Control/Development Laboratory records.\n\n10. Write and review Standard Operating Procedures related to Quality Systems within Manufacturing and QC/Development.\n\n11. Responsible for the development and issuance of Quality operational metrics.\n\n12. Represent Quality Assurance at various project and technical meetings.\n\n13. Must perform other duties as assigned by supervision. Responsible for notifying supervision when issues arise.\n\n14. Comply with quality and safety management systems including requirements for documentation, training, system use, SOPs, processes, and procedures\n\nBenefits\nDental insurance - effective day one of employment\n\nHealth insurance - effective day one of employment\n\nVision insurance - effective day one of employment\n\nHealth savings account\n\nLife & AD&D insurance\n\nShort & long term disability\n\nPaid time off & holidays\n\nEmployee Assistance Program\n\nTuition assistance\n\nSam's Club Basic membership reimbursement\n401(k) with company match\n\nSingota Solutions is an Equal Opportunity Employer","datePosted":"2026-08-11T10:44:47.919Z","dateModified":"2026-08-11T10:44:47.919Z","hiringOrganization":{"@type":"Organization","name":"Singota Solutions","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bloomington","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"3ee9e5f96ff95676ea9466f3"},"url":"https://jobsearcher.com/jobs/3ee9e5f96ff95676ea9466f3"}}