86 assurance associate jobs at 58 companies in Smithfield, RI
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Senior Associate, Quality Assurance
Bedford, Massachusetts, United States
$109k-$121k/yrOnsiteFull Time
Ocular TherapeutixNASDAQ: OCUL: Develops hydrogel-based drug delivery systems for treating eye diseases
5+ YOEBachelor's in a scientific discipline, 5+ years pharma/biotech/medical device QA experience, strong GMP/GLP knowledge, analytical testing familiarity, OOS/CAPA experience, and proficiency with MS Office.
Microsoft Office, Microsoft Excel, Microsoft PowerPoint
Charles River Center: Provides residential and vocational support for people with disabilities.
3+ YOE3+ years human services experience preferred; experience with DDS regulations, audits, data analysis, documentation review, training, and quality improvement.
ReplimuneNASDAQ: REPL: Develops oncolytic immunotherapies for cancer treatment.
3+ YOEBA/BS or equivalent, minimum 3 years pharma/biotech regulated experience with 3 years in QA/QC/manufacturing, working knowledge of cGMP and GDP, strong communication and multitasking skills.
PwC: Providing audit, tax, and management consulting services to businesses.
2+ YOEBachelor's degree, 2+ years experience, proficiency in QA methodologies including automation and testing for AI-enabled applications; experience with Selenium, data validation, and strong analytical and communication skills.
AbbottNYSE: ABT: Manufactures medical devices, diagnostics, and nutritional health products.
5+ YOEAssociate degree in engineering (or equivalent), 5+ years quality supervisory experience in medical devices or pharma, auditing experience, FDA/QMS compliance, strong communication and organizational skills.
AbbottNYSE: ABT: Provides medical devices, diagnostics, and science-based nutritional products.
5+ YOE5+ MgmtAssociate degree in engineering or equivalent, 5+ years quality supervisory experience in medical devices/pharma, quality systems/auditing experience, FDA compliance knowledge, strong communication and organizational skills.
Genetix Biotherapeutics: Developing and commercializing curative gene therapies for rare diseases.
4+ YOEBachelor's degree in life sciences, engineering, or related field; 4-6 years of QA experience in GMP-regulated biopharmaceutical or cell/gene therapy manufacturing; CMO oversight experience and cGMP knowledge.
Mass General Brigham: Provides integrated medical care, research, and clinical training services.
5+ YOEAssociate or Bachelor in Health Sciences; MA Radiography/Mammography license; ARRT-R and ARRT-M; 5-7 years radiology or related leadership/quality experience.
ZOLL Medical: Manufactures medical devices and software for emergency care.
4+ YOESupervise QA technicians, review and close product complaints, perform root cause and failure analysis, and coordinate corrective actions; 4+ years experience and associate's degree preferred; knowledge of FDA QSR and MS Office.
MS Windows, Microsoft Excel, Microsoft Access, Microsoft PowerPoint, Microsoft Word
Associate Director, Manufacturing Process and Technical Quality Assurance Cell and Genetic Therapies - VCGT
Boston, Massachusetts, United States
$157k-$235k/yrHybridFull Time
Vertex PharmaceuticalsNASDAQ: VRTX: Develops and sells prescription drugs for serious genetic diseases.
8+ YOEBachelor’s degree in a scientific or allied health field and 8+ years in a regulated pharmaceutical environment, with GxP quality assurance, cell therapy, investigations, risk management, and process lifecycle experience.
MES, eQMS, LIMS, data visualization platforms, process monitoring tools, advanced analytics, AI-enabled solutions
Candel TherapeuticsNASDAQ: CADL: Develops viral immunotherapies for the treatment of cancer.
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
AmgenNASDAQ: AMGN: Develops and manufactures biotechnology medicines for serious diseases.
4+ YOEHigh school/GED plus 4 years, associate degree plus 2 years, bachelor's plus 6 months, or master's, in QA or manufacturing experience; cGMP, GMP documentation, data integrity, analytical testing, and Microsoft Office preferred.
Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Teams
Cogent BiosciencesNASDAQ: COGT: Develops precision therapies for genetically defined diseases
8+ YOEProvide GCP QA leadership, lead audits and inspection readiness, manage CAPAs and vendor oversight; requires 8+ years GCP QA experience and a scientific bachelor's degree.
Bristol Myers SquibbNew York Stock Exchange: BMY: Develops and distributes innovative medicines for serious diseases.
4+ YOE4+ years cGMP experience (1+ year site manufacturing preferred). Bachelor's in STEM preferred (HS/Associates with experience considered). Proficiency with quality systems, data interpretation, MS Office and digital tools; strong communication and decision-making skills.
BMSDocs, CELabs, MES, SAP, ValG, DeltaV, Maximo, Infinity, Microsoft Power Automate, Smartsheet, Tableau, MS Office
Leonardo DRSNASDAQ: DRS: Manufactures advanced electronic systems for defense and military applications.
Associate degree in technical discipline or equivalent experience; strong decision-making and leadership; handling of small components; ESD practices; soldering/wire bonding a plus; safe handling of chemicals; proficiency in Access, Excel, and LabVIEW; MRPs experience a plus; good mechanical skills.
HologicNASDAQ: HOLX: Develops medical technology for women's healthcare and diagnostics.
Experience in quality assurance, quality systems, CAPA, root cause analysis, audits, data analysis, KPIs, procedures, training materials, and regulated industries; strong communication and independent judgment required.
Quality Management Systems (QMS), Corrective and Preventive Action (CAPA), Quality Plans (QPLs), Key Performance Indicators (KPIs)
Genezen: Produces viral vectors for cell and gene therapy programs.
6+ YOEBachelor's degree in science or related field; 6–8+ years in pharmaceutical or biologics quality assurance; GMP, investigations, quality systems, cross-functional leadership, and mentoring experience.
Veeva, 21 CFR Part 11, 21 CFR 210, 21 CFR 211, 21 CFR 600, 21 CFR 610, EudraLex Volume 4, ICH Quality Guidelines, EMA, ISO
TeleflexNYSE: TFX: Manufactures medical devices for critical care and surgical procedures.
1+ YOE1+ year training/document control or quality support experience in a regulated industry; high school diploma (associate preferred); knowledge of QMS, controlled documentation, FDA and ISO 13485 requirements; strong accuracy and reporting skills.