{"schemaVersion":"jobsearcher.job.v1","id":"b656c331a6493bc563e9768f","url":"https://jobsearcher.com/jobs/b656c331a6493bc563e9768f","canonicalUrl":"https://jobsearcher.com/jobs/b656c331a6493bc563e9768f","title":"Analytical QA Associate","description":"Job Description\nJob Title: Quality Assurance (QA) Associate III – Analytical\nWork Location: Fall River, MA\nJob Purpose\nThe purpose of the QA Associate III - Analytical position is to monitor and ensure product and analytical quality is maintained throughout all phases of the analysis process in compliance with established specifications and standard operating procedures (SOPs).\nDuties and Responsibilities\nReview data generated in the laboratory is accordance with stablished criteria set forth in SOPs and\n· established specifications\nAssemble quality data to support management review meeting requirements\nIssuing, reviewing, maintaining, and archiving of laboratory logbooks\nScanning of laboratory approved finalized qualification for easy accessibility by all department\nTraining and execution of internal audits, as required\nReview/approval of calibration records for analytical instrumentation and equipment\nIdentify and report any non-conformances and/or discrepancies to management if applicable.\nComplete other duties or participate in project work as assigned by management.\nEducation and Experience\nMinimum bachelor’s degree from an accredited college/university in relevant field of study such as Chemistry,\nPharmaceutical Science, or other Life Science discipline.\nAdvanced training or education in pharmaceutical quality compliance or related field of study from an\naccredited college/university.is preferred.\nMinimum of three (3) years’ experience in quality assurance in a current Good Manufacturing Practice (cGMP)\npharmaceutical work environment.\nExperience in metered dose inhalation (MDI) preferred.\nProficient user of personal computer hardware and software applications such as Microsoft Office tools, SAP,\nand other business applications.\nPhysical and Work Schedule Requirements\nIndependent, unassisted lifting up to 10 kg, may be required.\nAble to always wear appropriate personal protective equipment (PPE) such as safety glasses, shoe covers,\nhard hat, lab coat and other PPE, when required.\nSitting at a desk and/or working at a computer or other \"screen\" 75% or greater of an 8-hour period.\nTypical work schedule is Monday through Friday, 9 AM to 5:30 PM. Some weekends may be required based\non business needs.\nProfessional and Behavioral Competencies\nMust be able to work under general supervision and able to work independently and in a team environment.\nMust be able to influence decision-making and facilitate completion of work toward the achievement of the business plan and goals.\nMust be able to exercise appropriate professional judgment on matters of significance.\nEffective interpersonal relationship skills and the ability to work in a team environment.\nProficiency in the English language to include usage, spelling, grammar, and punctuation.\nMust have current Good Manufacturing Practices (cGMP) knowledge.\nMust have strong attention-to-detail.\nMust be a self-starter and demonstrate initiative with seeking additional training or direction as needed.\nMust have strong organization and communication skills (written, verbal, and presentation).\nMust be detail-oriented with the ability to multitask and prioritize tasks with strict deadlines.\nNo employment sponsorship or work visas.\nMUST HAVES:\nMinimum bachelor’s degree from an accredited college/university in relevant field of study such as Chemistry,\nPharmaceutical Science, or other Life Science discipline.\nAdvanced training or education in pharmaceutical quality compliance or related field of study from an\naccredited college/university.is preferred.\nMinimum of three (3) years’ experience in quality assurance in a current Good Manufacturing Practice (cGMP)\npharmaceutical work environment.\nExperience in metered dose inhalation (MDI) preferred.\nJob Type: Full-time\nPay: $70,000.00 - $75,000.00 per year\nBenefits:\n401(k)\n401(k) matching\nDental insurance\nHealth insurance\nPaid time off\nRelocation assistance\nVision insurance\nSchedule:\n8 hour shift\nDay shift\nMonday to Friday\nExperience:\nPharmaceutical: 5 years (Preferred)\nhplc: 3 years (Preferred)\nQA Associate: 5 years (Preferred)\nWork Location: In person","company":"Staid Logic","rawCompany":"staid logic","city":"Fall River","state":"MA","isRemote":false,"isActive":false,"createdAt":"2026-04-12T20:37:22.809Z","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":"325411","title":"Medicinal and Botanical Manufacturing","slug":"medicinal-and-botanical-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Analytical QA Associate","description":"Job Description\nJob Title: Quality Assurance (QA) Associate III – Analytical\nWork Location: Fall River, MA\nJob Purpose\nThe purpose of the QA Associate III - Analytical position is to monitor and ensure product and analytical quality is maintained throughout all phases of the analysis process in compliance with established specifications and standard operating procedures (SOPs).\nDuties and Responsibilities\nReview data generated in the laboratory is accordance with stablished criteria set forth in SOPs and\n· established specifications\nAssemble quality data to support management review meeting requirements\nIssuing, reviewing, maintaining, and archiving of laboratory logbooks\nScanning of laboratory approved finalized qualification for easy accessibility by all department\nTraining and execution of internal audits, as required\nReview/approval of calibration records for analytical instrumentation and equipment\nIdentify and report any non-conformances and/or discrepancies to management if applicable.\nComplete other duties or participate in project work as assigned by management.\nEducation and Experience\nMinimum bachelor’s degree from an accredited college/university in relevant field of study such as Chemistry,\nPharmaceutical Science, or other Life Science discipline.\nAdvanced training or education in pharmaceutical quality compliance or related field of study from an\naccredited college/university.is preferred.\nMinimum of three (3) years’ experience in quality assurance in a current Good Manufacturing Practice (cGMP)\npharmaceutical work environment.\nExperience in metered dose inhalation (MDI) preferred.\nProficient user of personal computer hardware and software applications such as Microsoft Office tools, SAP,\nand other business applications.\nPhysical and Work Schedule Requirements\nIndependent, unassisted lifting up to 10 kg, may be required.\nAble to always wear appropriate personal protective equipment (PPE) such as safety glasses, shoe covers,\nhard hat, lab coat and other PPE, when required.\nSitting at a desk and/or working at a computer or other \"screen\" 75% or greater of an 8-hour period.\nTypical work schedule is Monday through Friday, 9 AM to 5:30 PM. Some weekends may be required based\non business needs.\nProfessional and Behavioral Competencies\nMust be able to work under general supervision and able to work independently and in a team environment.\nMust be able to influence decision-making and facilitate completion of work toward the achievement of the business plan and goals.\nMust be able to exercise appropriate professional judgment on matters of significance.\nEffective interpersonal relationship skills and the ability to work in a team environment.\nProficiency in the English language to include usage, spelling, grammar, and punctuation.\nMust have current Good Manufacturing Practices (cGMP) knowledge.\nMust have strong attention-to-detail.\nMust be a self-starter and demonstrate initiative with seeking additional training or direction as needed.\nMust have strong organization and communication skills (written, verbal, and presentation).\nMust be detail-oriented with the ability to multitask and prioritize tasks with strict deadlines.\nNo employment sponsorship or work visas.\nMUST HAVES:\nMinimum bachelor’s degree from an accredited college/university in relevant field of study such as Chemistry,\nPharmaceutical Science, or other Life Science discipline.\nAdvanced training or education in pharmaceutical quality compliance or related field of study from an\naccredited college/university.is preferred.\nMinimum of three (3) years’ experience in quality assurance in a current Good Manufacturing Practice (cGMP)\npharmaceutical work environment.\nExperience in metered dose inhalation (MDI) preferred.\nJob Type: Full-time\nPay: $70,000.00 - $75,000.00 per year\nBenefits:\n401(k)\n401(k) matching\nDental insurance\nHealth insurance\nPaid time off\nRelocation assistance\nVision insurance\nSchedule:\n8 hour shift\nDay shift\nMonday to Friday\nExperience:\nPharmaceutical: 5 years (Preferred)\nhplc: 3 years (Preferred)\nQA Associate: 5 years (Preferred)\nWork Location: In person","datePosted":"2026-04-12T20:37:22.809Z","dateModified":"2026-04-12T20:37:22.809Z","hiringOrganization":{"@type":"Organization","name":"Staid Logic","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Fall River","addressRegion":"MA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"b656c331a6493bc563e9768f"},"url":"https://jobsearcher.com/jobs/b656c331a6493bc563e9768f"}}