25 qa specialist jobs at 19 companies in Putnam, 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.
3d
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QA Labeling Specialist
Milford or Maine or Massachusetts or Maryland or Tipperary County or Oxford or Traverse City
$55k-$82k/yr OnsiteFull Time
2+ YOEBachelor’s degree or equivalent experience, 2+ years in a regulated medical product environment, and proficiency with Microsoft Word, Excel, Adobe InDesign, and/or NiceLabel Pro. Knowledge of FDA and ISO requirements preferred.
Microsoft Word, Microsoft Excel, Adobe InDesign, NiceLabel Pro, ETQ
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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.
5d
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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
2mo
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Senior Specialist, Field Quality QA Operations
Devens, Massachusetts, United States
$90k-$108k/yr OnsiteFull Time
4+ YOE4 years QA experience in pharma/medical device, batch record review experience, knowledge of US/EU cGMP, ability to perform on-floor GMP walkthroughs, and familiarity with electronic batch record systems (DeltaV desirable). Bachelor's degree preferred.
DeltaV
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QA Specialist- Documentation
Waltham, Massachusetts, United States
$110k-$170k/yr OnsiteFull Time
5+ YOEBachelor's degree in a relevant field, 5+ years of GxP quality assurance experience, SOP and controlled document management, Veeva Vault QMS proficiency, FDA and ICH knowledge, and strong communication and organizational skills.
Veeva Vault QMS, Microsoft Office Suite, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook
2mo
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Senior Specialist, Field Quality QA Operations
Devens, Massachusetts, United States
$90k-$108k/yr OnsiteFull Time
4+ YOEMinimum 4 years QA experience in pharmaceutical or medical device manufacturing, batch record review experience, knowledge of US/EU cGMP, familiarity with electronic/paper batch record systems and DeltaV; bachelor's degree preferred.
DeltaV
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QA Specialist - Lot Disposition, Site Based, Redmond, WA
Redmond or Seattle or Watertown or Alderley Park or United Kingdom or United States
$90k-$100k/yr OnsiteFull Time
3+ YOEBachelor's degree in biological or engineering science and 3+ years in biopharmaceutical or pharmaceutical cGMP manufacturing; requires cross-functional communication and strong analytical and organizational skills.
cGMPs
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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.
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)
4w
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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
1mo
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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.
2w
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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
2w
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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
3w
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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)
3w
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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%.
4w
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Senior Quality Assurance Document Specialist
Needham, Massachusetts, United States
$143k-$155k/yr HybridFull Time
6+ YOE6+ years QA experience with BS/BA in scientific or engineering (or 8+ years with Associate); knowledge of 21 CFR Part 11/Annex 11/CFR210/211, GxP, eQMS, internal audit, and regulatory guidelines; strong communication and organizational skills.
Electronic Quality Management System (eQMS), SmartSheet, SharePoint, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Microsoft Teams
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