17 qa specialist jobs at 13 companies in Moosup, CT
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GLP QA Specialist II
Fall River, Massachusetts, United States
$88k-$114k/yr OnsiteFull Time
1+ YOEBS in life sciences preferred,1-3 years QA experience in biotech/pharma,knowledge of EDMS,cGMP/GLP,Microsoft Word and Excel,excellent communication and ability to work independently.
EDMS, Microsoft Word, Microsoft Excel
1mo
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Clinical QA Specialist
Newark or Marlborough
$85k-$133k/yr OnsiteFull Time
5+ YOEBachelor's degree in a related field, 5+ years in medical device or healthcare QA with adverse event reporting, CAPA experience, knowledge of FDA QSR/ISO 13485/ISO 14971/MDR, strong communication and analytical skills.
1mo
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Sr Specialist QA - Compliance
West Greenwich, Rhode Island, United States
$132k-$179k/yr OnsiteFull Time
6+ YOECoordinate site inspection readiness and logistics for regulatory inspections and audits; knowledge of cGMP, quality systems, auditing, data analysis, and project management; bachelor's degree plus experience or equivalent combinations as listed.
1d
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Specialist I, QA Compliance
Canton, Massachusetts, United States
$129k-$156k/yr OnsiteFull Time
6+ YOEBachelor’s degree in a scientific or related field, six years of cGMP quality experience, commercial large-molecule manufacturing experience, pharmaceutical regulations, ISO standards, GMP expertise, and PC software proficiency.
Microsoft PowerPoint, Microsoft Excel, Microsoft Word, Microsoft Outlook, Internet Explorer, Microsoft Access, Microsoft Visio, PC
4w
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Quality Specialist I/II
Providence, Rhode Island, United States
$58k-$78k/yr OnsiteFull Time
2+ YOEImplements and maintains QMS, performs QA activities, investigates deviations, supports validations, audits, supplier qualification, and regulatory inspections; requires relevant life-science education and 2+ years QA/manufacturing or clinical experience.
1w
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QA/Expeditor - Middletown Chili's
Middletown, Rhode Island, United States
$16-$21/hr OnsiteFull Time
Dependable team player with strong multitasking, communication, and teamwork skills; comfortable in a fast-paced environment. No experience necessary.
1mo
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Quality Assurance Specialist
New London, Connecticut, United States
$20-$25/hr OnsiteFull Time
Perform inspections and tests on raw materials and finished goods, document non-conformities, participate in audits, support QA process development, and maintain regulatory compliance in a pharmaceutical setting.
3mo
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Quality Assurance Specialist
Holyoke, Massachusetts, United States
$60k-$80k/yr OnsiteFull Time
3+ YOE3+ years regulatory compliance management; 5+ years QA/QC experience; degree in related field; knowledge of GMP/HACCP; driver’s license; strong communication and computer skills.
Microsoft Office
1w
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Quality Assurance Specialist
Rocky Hill, Connecticut, United States
$18/hr OnsiteFull Time
0+ YOEHigh school diploma or GED required; 1 year of laboratory QA or 2 years of manufacturing experience. Must be U.S.-authorized, 21+, computer proficient, and able to lift 25 pounds.
cGMP, SQF, Material Safety Data Sheets (MSDS), Standard Operating Procedures (SOP)
3w
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Senior eCommerce UAT Specialist
Manchester or Massachusetts or Connecticut
$90k-$110k/yr HybridFull Time
7+ YOE7+ years eCommerce QA/UAT experience, UAT strategy and execution, test planning, defect tracking, API and cross-device testing, leadership and mentoring skills.
Tosca, Playwright, Selenium, JIRA, Asana, Panaya, Postman, SoapUI, Google Analytics, Bloomreach, SAP Commerce Cloud (Hybris), SAP ERP
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Quality Assurance Specialist I
Milford or Ohio
$58k-$71k/yr OnsiteFull Time
1+ YOEKnowledge of cGMP/ICH Q7, experience writing/reviewing GMP documents, BS/BA in science or Associate plus experience, 1-5+ years QA cGMP experience, strong communication and problem solving.
1w
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Associate Quality Production Specialist (FAI)
Enfield, Connecticut, United States
$59k-$84k/yr OnsiteFull Time
3+ YOERequires 3+ years of quality experience, 2+ years using QA inspection methods, First Article Inspection, calipers, gages, and comparators, plus blueprint interpretation, AS9100/AS91023 knowledge, and Microsoft Office skills.
Microsoft Outlook, Microsoft Excel, calipers, ring gages, pin gages, comparator, Microsoft Office, GD&T
1w
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Associate Quality Production Specialist (FAI)
Enfield, Connecticut, United States
$59k-$84k/yr OnsiteFull Time
3+ YOERequires 3+ years of quality experience, 2+ years using QA inspection methods including First Article Inspection, blueprint interpretation, measurement tools, AS9100/AS91023 knowledge, Microsoft Office, and U.S. Person status.
calipers, ring gages, pin gages, comparator, Microsoft Office, Microsoft Outlook, Microsoft Excel, GD&T
2w
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Principal Clinical Quality Assurance Specialist
Maple Grove or Arden Hills or Marlborough
$117k-$222k/yr HybridFull Time
5+ YOEBachelor's degree, 5+ years clinical QA experience including GCP audits, working knowledge of ISO 14155/13485/GCP/GMP/GDP, CAPA and quality systems experience, ability to travel up to 30%.
ISO 14155, ISO 13485, Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), Good Documentation Practice (GDP)
2w
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Principal Clinical Quality Assurance Specialist
Marlborough or Arden Hills or Maple Grove
$117k-$222k/yr HybridFull Time
5+ YOE5+ years clinical QA experience including conducting GCP/regulatory audits, knowledge of ISO 14155/13485/GCP/GMP, CAPA and inspection readiness; bachelor's degree required and ability to travel up to 30%.
2mo
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Packaging Specialist (Rocky Hill, CT, US, 06067)
Rocky Hill, Connecticut, United States
OnsiteFull Time
1+ YOE1+ years related experience; accurately weighing, assembling, packaging, sealing, and labeling cannabis products; operating flow wrap, labeling, and heat-sealing machines; following SOPs, QA sampling, standing long periods, lifting up to 25 lb, and registering as a state cannabis agent.
flow wrap, labeling machine, heat-sealing machine, track and trace system
3w
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Principal Clinical Quality Assurance Specialist
Marlborough, Massachusetts, United States
$117k-$222k/yr HybridFull Time
5+ YOEBachelor's degree in science/engineering/health-related field, 5+ years clinical QA or clinical research compliance experience, 5+ years conducting GCP/regulatory audits, knowledge of ISO 14155/13485/GCP/GMP/GDP, CAPA and quality systems experience.
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