{"schemaVersion":"jobsearcher.job.v1","id":"e089895b0c8ab4556a3a0b9d","url":"https://jobsearcher.com/jobs/e089895b0c8ab4556a3a0b9d","canonicalUrl":"https://jobsearcher.com/jobs/e089895b0c8ab4556a3a0b9d","title":"QA Coordinator (2nd Shift)","description":"Pay Rate Low: 23.00 | Pay Rate High: 23.00\r\nQuality Control Technician – 2nd Shift\r\nOur client, a Fortune 500 industry leader, is seeking a Quality Assurance Coordinator to join their team. This is an exciting opportunity to contribute to innovative work across the biopharma, healthcare, and advanced technologies industries while supporting critical laboratory and quality operations in a GMP-regulated environment.\r\nPosition Details\r\nPay Rate: $23.00/hour\r\nShift: 2nd Shift | Monday–Friday | 3:00 PM – 11:30 PM\r\nWork Environment: Onsite\r\nPosition Summary\r\nThe Quality Assurance Coordinator is responsible for performing analytical testing and supporting quality operations to ensure timely and accurate results for raw materials, intermediates, and finished products. This role supports cGMP, ISO, and quality system compliance while collaborating with cross-functional teams to maintain operational excellence and product quality.\r\nKey Responsibilities\r\nPerform timely analysis of testing samples and report accurate results\r\nConduct sampling and testing of raw materials, intermediates, and finished goods\r\nSupport coordination with toll manufacturers regarding quality-related questions and issues\r\nEnsure compliance with analytical testing requirements (ATR)\r\nAssist with ISO implementation and quality system initiatives\r\nPrepare and standardize laboratory solutions, standards, and calibration activities\r\nOperate and support analytical instrumentation including HPLC, GC, and wet chemistry testing\r\nEnter and maintain analytical results and documentation within SAP\r\nComplete and maintain all required GMP and ISO documentation and logbooks\r\nSupport batch timeline, quality, and production goals\r\nPromote safe laboratory operations and maintain zero-incident standards\r\nAssist in training and supervising operators within the department\r\nParticipate as a member of the Emergency Response Team and support emergency preparedness activities\r\nMaintain compliance with ISO 9001, ISO/IEC 17025, cGMP, and internal quality systems\r\nMinimum Qualifications\r\nHigh school diploma or equivalent\r\n1–2 years of experience in Quality within a regulated manufacturing environment\r\nExperience supporting cGMP, ISO, and regulatory audit activities\r\nPreferred Qualifications\r\nExperience in Quality Control within fine chemical or pharmaceutical manufacturing environments\r\nWorking knowledge of cGMP regulations and laboratory quality systems\r\nHands-on experience with HPLC, GC, and wet chemistry analysis\r\nSkills & Competencies\r\nStrong attention to detail and organizational skills\r\nEffective communication and teamwork abilities\r\nWillingness to learn and adapt in a fast-paced environment\r\nCommitment to safety, quality, and continuous improvement\r\nThis job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you.\r\nJ-18808-Ljbffr","company":"Astrix","rawCompany":"astrix","city":"Carpinteria","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-07-04T03:06:31.860Z","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":"19-4031.00","title":"Chemical Technicians","slug":"chemical-technicians"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325413","title":"In-Vitro Diagnostic Substance Manufacturing","slug":"in-vitro-diagnostic-substance-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"QA Coordinator (2nd Shift)","description":"Pay Rate Low: 23.00 | Pay Rate High: 23.00\r\nQuality Control Technician – 2nd Shift\r\nOur client, a Fortune 500 industry leader, is seeking a Quality Assurance Coordinator to join their team. This is an exciting opportunity to contribute to innovative work across the biopharma, healthcare, and advanced technologies industries while supporting critical laboratory and quality operations in a GMP-regulated environment.\r\nPosition Details\r\nPay Rate: $23.00/hour\r\nShift: 2nd Shift | Monday–Friday | 3:00 PM – 11:30 PM\r\nWork Environment: Onsite\r\nPosition Summary\r\nThe Quality Assurance Coordinator is responsible for performing analytical testing and supporting quality operations to ensure timely and accurate results for raw materials, intermediates, and finished products. This role supports cGMP, ISO, and quality system compliance while collaborating with cross-functional teams to maintain operational excellence and product quality.\r\nKey Responsibilities\r\nPerform timely analysis of testing samples and report accurate results\r\nConduct sampling and testing of raw materials, intermediates, and finished goods\r\nSupport coordination with toll manufacturers regarding quality-related questions and issues\r\nEnsure compliance with analytical testing requirements (ATR)\r\nAssist with ISO implementation and quality system initiatives\r\nPrepare and standardize laboratory solutions, standards, and calibration activities\r\nOperate and support analytical instrumentation including HPLC, GC, and wet chemistry testing\r\nEnter and maintain analytical results and documentation within SAP\r\nComplete and maintain all required GMP and ISO documentation and logbooks\r\nSupport batch timeline, quality, and production goals\r\nPromote safe laboratory operations and maintain zero-incident standards\r\nAssist in training and supervising operators within the department\r\nParticipate as a member of the Emergency Response Team and support emergency preparedness activities\r\nMaintain compliance with ISO 9001, ISO/IEC 17025, cGMP, and internal quality systems\r\nMinimum Qualifications\r\nHigh school diploma or equivalent\r\n1–2 years of experience in Quality within a regulated manufacturing environment\r\nExperience supporting cGMP, ISO, and regulatory audit activities\r\nPreferred Qualifications\r\nExperience in Quality Control within fine chemical or pharmaceutical manufacturing environments\r\nWorking knowledge of cGMP regulations and laboratory quality systems\r\nHands-on experience with HPLC, GC, and wet chemistry analysis\r\nSkills & Competencies\r\nStrong attention to detail and organizational skills\r\nEffective communication and teamwork abilities\r\nWillingness to learn and adapt in a fast-paced environment\r\nCommitment to safety, quality, and continuous improvement\r\nThis job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you.\r\nJ-18808-Ljbffr","datePosted":"2026-07-04T03:06:31.860Z","dateModified":"2026-07-04T03:06:31.860Z","hiringOrganization":{"@type":"Organization","name":"Astrix","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Carpinteria","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"e089895b0c8ab4556a3a0b9d"},"url":"https://jobsearcher.com/jobs/e089895b0c8ab4556a3a0b9d"}}