36 qa director jobs at 27 companies in Dighton, MA

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Sr Director, QA- GxP Systems
Needham, Massachusetts, United States
$258k-$280k/yr HybridFull Time
Candel Therapeutics
Candel TherapeuticsNASDAQ: CADL: Develops viral immunotherapies for the treatment of cancer.
10+ YOEBachelor's in life sciences,10+ years biotech/pharma QA with GxP systems, vendor oversight, CSV, audits, and Part 11 compliance; experience with eQMS/EDMS and regulated clinical workflows.
eQMS, EDMS
1w
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Director, QA for QC
Cambridge, Massachusetts, United States
$213k-$260k/yr HybridFull Time
Intellia Therapeutics
Intellia TherapeuticsNASDAQ: NTLA: Develops curative gene-editing treatments using CRISPR technology.
10+ YOE10+ years industry experience with GMP QC oversight; advanced degree (MS/PhD preferred); experience with stability, reference standards, analytical methods, audits, and regulatory interactions.
EDMS, LIMS, JMP, MINITAB, GraphPad Prism, PLA, HPLC, UPLC, CE
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Associate Director, GMP QA Operations
Waltham, Massachusetts, United States
$160k-$195k/yr OnsiteFull Time
Dyne Therapeutics
Dyne TherapeuticsNASDAQ: DYN: Developing therapeutics for genetically driven neuromuscular diseases.
8+ YOEBachelor's in engineering/science (Master's preferred), 8+ years in cGMP environment and 5+ years in QA, experience overseeing CMOs/CDMOs, knowledge of FDA/EMA regulations, GxP QA systems, strong communication and decision-making skills.
Microsoft Office, SmartSheet, Veeva
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Associate Director, GCP/GLP/GVP QA
Boston, Massachusetts, United States
$160k-$240k/yr HybridFull Time
Rhythm Pharmaceuticals
Rhythm PharmaceuticalsNASDAQ: RYTM: Develops precision medicines for rare neuroendocrine and obesity diseases.
8+ YOE8+ years industry experience with 5+ years GCP QA or clinical trial QA, experience with GCP/GLP/GVP regulations and regulatory inspections, strong communication and project management skills.
2w
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Director/Senior Director, QMS, Digital QA and GxP Compliance
Waltham, Massachusetts, United States
$200k-$260k/yr OnsiteFull Time
Crescent Biopharma
Crescent BiopharmaNASDAQ: CBIO: Develops novel oncology therapies and antibody-drug conjugates for cancer.
8+ YOEBachelor's degree,8+ years in QMS and digital QA in biotech/pharma,expertise in GxP computerized systems,validation,data integrity,vendor qualification,audit and inspection readiness.
GAMP
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Associate Director, QA Manufacturing Technical Services
Boston, Massachusetts, United States
$157k-$235k/yr OnsiteFull Time
Vertex Pharmaceuticals
Vertex PharmaceuticalsNASDAQ: VRTX: Develops and sells prescription drugs for serious genetic diseases.
8+ YOEBachelor's in biotech/life sciences required (Master's preferred), typically 8+ years' industry experience in manufacturing/QA/QC for biotech/pharma, strong GxP/cGMP knowledge, deviation/CAPA/root-cause expertise, and electronic QMS experience.
QMS, Trackwise, Veeva, cGMP, GXP, LEAN, DMAIC, Six Sigma
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Little People's College, Inc. - Program Director
Acushnet or Fairhaven or Mattapoisett or Wareham
$47k-$55k/yr OnsiteFull Time
Little People's College
Little People's College: Operates early education and childcare centers for young children.
5+ YOE3+ MgmtEEC Director I certification; Bachelor's in Early Childhood Education or related field (preferred); 5 years licensed ECE; 3 years leadership; licensing/QA experience desirable.
3mo
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Senior Quality Director
Waltham, Massachusetts, United States
$220k-$300k/yr HybridFull Time
Nova Biomedical
Nova Biomedical: Develops and manufactures blood testing analyzers and diagnostic equipment.
12+ YOE12+ Mgmt12+ years medical device/diagnostic QA experience with 12+ years managing quality teams; strong GMP, QMS, CAPA, audits, root cause analysis, validation, supplier and training oversight.
LMS
2d
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Associate Director/Director, Technical Quality
Charlestown or United States
$190k-$230k/yr HybridFull Time
Solid Biosciences
Solid BiosciencesNASDAQ: SLDB: Develops precision genetic medicines for neuromuscular and cardiac diseases.
10+ YOE3+ MgmtRequires a science-related bachelor's degree or equivalent experience, 10–15 years of biotech technical QA experience, 3+ years leading outsourced activities, GMP expertise, biologics experience, and regulatory inspection experience.
GMP, GDP, SOPs, CAPAs, AAV
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Director, Quality Assurance
Lexington, Massachusetts, United States
$170k-$218k/yr OnsiteFull Time
Agenus
AgenusNASDAQ: AGEN: Developing immuno-oncology therapies and vaccines to treat cancer.
10+ YOEBachelor's in a scientific discipline,10+ years QA experience in biotech/pharma, GMP/GCP/GLP expertise, eQMS experience, CMO oversight, inspection readiness, and leadership skills.
ZenQMS
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Director of Quality
Chelsea, Massachusetts, United States
$169k-$258k/yr OnsiteFull Time
Catalent
Catalent: Global provider of drug development and manufacturing solutions.
10+ YOEBachelor's in chemistry/biology required, master's preferred; 10+ years leading QA/QC in pharmaceutical GMP; regulatory inspection experience; knowledge of change management and Lean; leadership and budget management skills.
Lean, Good Manufacturing Practice (GMP), GEA Niro SD1, GEA Niro SD4, GEA Niro SD7, Dry Powder Inhaler (DPI)
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Associate Director, Programmatic
Boston or Charlotte or Chicago or Denver or New York or Salt Lake City or Colorado or Texas or Massachusetts or North Carolina or Utah or Illinois or New York or Florida or United States
$96k-$130k/yr RemoteFull Time
DEPT
DEPT: Global digital agency providing integrated technology and marketing services.
5+ YOE5+ years programmatic agency experience, advanced proficiency with The Trade Desk, DV360, Amazon DSP and Google Ads/YouTube, team leadership, campaign architecture, QA, launch management, and operational/process development.
The Trade Desk, DV360, Amazon DSP, Google Ads, YouTube, Trello
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Director, Clinical Compliance
San Francisco or Seattle or Boston
$210k-$235k/yr RemoteFull Time
Jade Biosciences
Jade BiosciencesNASDAQ: JBIO: Developing best-in-class therapies for autoimmune diseases.
10+ YOEAdvanced degree plus senior-level experience in clinical operations/QA (10+ years relevant). Strong knowledge of ICH-GCP, vendor/CRO oversight, audit/inspection support, CAPA development, and leadership skills.
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Associate Director, Quality Compliance
Somerville, Massachusetts, United States
$144k-$195k/yr HybridFull Time
Genetix Biotherapeutics
Genetix Biotherapeutics: Developing and commercializing curative gene therapies for rare diseases.
10+ YOEBachelor's degree with 10+ years QA/GxP experience; strong validation and product lifecycle expertise; in-depth US/EU GMP and ICH knowledge; experience with CMOs/CTOs and inspection readiness.
3mo
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Director, Product Quality Lead
Waltham, Massachusetts, United States
$212k-$235k/yr OnsiteFull Time
Innoviva Specialty Therapeutics
Innoviva Specialty TherapeuticsNASDAQ: INVA: Develops therapies for critical care and infectious diseases.
10+ YOEB.S. in a scientific/technical field, 10+ years pharma experience (7+ in QA/GMP), expertise with small-molecule product quality, inspection readiness, regulatory submissions, and proficiency with document management systems and Microsoft Office.
document management systems, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
1mo
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Associate Director, GMP Quality
San Francisco or Boston
$160k-$180k/yr OnsiteFull Time
Olema Oncology
Olema OncologyNASDAQ: OLMA: Develops targeted therapies for women's cancers.
8+ YOEBachelor's required (advanced degree preferred),8+ years in pharmaceutical GMP/GMP QA, knowledge of cGMP, small-molecule experience, NDA/BLA submission experience, quality systems familiarity, strong leadership and communication.
Veeva, TrackWise, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft SharePoint
2mo
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Associate Director, Early Development Quality Lead, R&D QA
Cambridge or United States
$165k-$223k/yr HybridFull Time
Alnylam Pharmaceuticals
Alnylam PharmaceuticalsNASDAQ: ALNY: Develops RNAi therapeutics to treat rare and common diseases.
8+ YOE8+ years relevant experience in bioanalytical/toxicology quality (GLP/GCP/GCLP); experience with assay development, risk-based QA, auditing, vendor oversight, and regulatory guidance across FDA/PMDA/EU/MHRA. Master's preferred.
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Senior Director, Corporate Quality – PV
Bedford, Massachusetts, United States
$222k-$278k/yr HybridFull Time
Sarepta Therapeutics
Sarepta TherapeuticsNASDAQ: SRPT: Develops precision genetic medicines for rare diseases.
15+ YOEBachelor's in life sciences with ~15 years in pharma/biotech drug development; minimum 10 years GCP/GVP QA (≥5 years focused GVP QA); clinical trial and inspection experience; QMS, SOPs, audit design, root-cause investigations, and strong technical writing skills.
2mo
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Associate Director, Development Quality Assurance
Carlsbad or Boston or Dublin or United States
$155k-$197k/yr HybridFull Time
Ionis Pharmaceuticals
Ionis PharmaceuticalsNASDAQ: IONS: Discovers and develops RNA-targeted medicines for serious diseases.
5+ YOEAdvanced degree and extensive GCP QA experience (varies by degree: BSc+12 yrs, MSc+8 yrs, PhD+5 yrs or equivalent). Strong knowledge of ICH/GCP, inspection readiness, audit conduct, CAPA management, risk-based QA, and ability to travel 30–40%.
2mo
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Director of Quality Improvement
Worcester, Massachusetts, United States
$62-$95/hr OnsiteFull Time
Tenet Healthcare
Tenet HealthcareNYSE: THC: Operates a network of hospitals and ambulatory care centers.
5+ YOERegistered Nurse with Bachelor's (or Master/Doctorate) in inpatient care field, 5 years QA/PI experience, current state license to practice, CPHQ or eligibility within two years, leadership and data/reporting experience.