22 qa director jobs at 15 companies in Nazareth, PA
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Associate QA Director
Durham or Indianapolis or Wayne
$89k-$247k/yrOnsiteFull Time
IQVIANYSE: IQV: Provides clinical research and data analytics for pharmaceutical companies.
10+ YOE10+ years GxP quality assurance experience in pharmaceutical/technical settings, audit experience, strong problem solving, risk analysis, communication and leadership skills.
Daiichi SankyoTokyo Stock Exchange: 4568: Global pharmaceutical developing innovative medicines for various diseases.
10+ YOE10+ MgmtBachelor's degree required (Master's preferred), 10+ years PV QA or related experience, strong knowledge of GCP/GVP/regulatory guidance, REMS oversight experience preferred, leadership and communication skills.
CytokineticsNASDAQ: CYTK: Develops muscle-directed medicines for cardiovascular and neuromuscular diseases.
10+ YOEBachelor's degree preferred; 10+ years in pharmaceutical manufacturing, team leadership, regulatory inspections or audits, global GMP regulations, MS Office, communication, organization, and independent decision-making.
North Chicago or Cambridge or Worcester or Florham Park or Irvine or San Francisco or United States
$142k-$269k/yrHybridFull Time
AbbVieNYSE: ABBV: Develops and sells innovative pharmaceutical and biopharmaceutical medicines.
7+ YOEBachelor’s degree in science or healthcare, 7+ years in pharmaceutical clinical development, regulatory affairs, or quality assurance, with extensive clinical regulations, auditing, leadership, and risk management expertise.
Tris Pharma: Develops and sells medicines for ADHD and neurological disorders.
12+ YOE8+ MgmtBachelor's degree in science or related field; 12–15 years of pharmaceutical or biotechnology quality experience, including 8–10 years of R&D or clinical QA leadership. Requires GxP, audit, inspection, and regulatory expertise.
Quality Management System (QMS), SOPs, CAPA, FDA, ICH Guidelines, EU Clinical Trial Regulation, EMA, MHRA, PMDA, GCP, GVP, GLP, GxP, ALCOA++, ALCOA+, clinical trial systems and technologies
SystImmune: Developing multi-specific antibodies and antibody-drug conjugates for cancer therapy
8+ YOEBachelor's degree in a relevant life sciences field, 8+ years in clinical quality or related pharmaceutical functions, and 5+ years of direct GCP quality assurance experience with audits and inspections.
Clinical Quality Management System (QMS), Risk-Based Quality Management (RBQM), Quality Tolerance Limits (QTLs), Standard Operating Procedures (SOPs)
Director, GPV Compliance & Business Management (QA)
Princeton, New Jersey, United States
$186k-$279k/yrOnsiteFull Time
Otsuka PharmaceuticalTokyo Stock Exchange: 4578: Develops and manufactures innovative pharmaceutical and nutritional products.
6+ YOEBachelor's degree required; minimum 6 years PV compliance or quality management experience; experience with GxP/GVP/GCP inspections, vendor oversight, global settings, CAPA/deviation management, audit readiness, and Microsoft Office proficiency.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook
Paratek Pharmaceuticals: Develops and sells antibiotic therapies for life-threatening infections.
15+ YOEBachelor's degree in chemistry, biology, or related field; 15+ years in pharmaceutical manufacturing, technical operations, or QA, including 12+ years of direct QA experience; strong cGMP and regulatory expertise.
Catalent: Global provider of drug development and manufacturing solutions.
Bachelor's in chemistry/engineering/natural sciences,10+ years pharmaceutical experience with leadership,extensive QA/QC knowledge,cGMP and ICH familiarity,ability to manage audits,inspections,and batch disposition.
Hajoca: Wholesale distributor of plumbing, heating, and industrial supplies.
10+ YOE5+ MgmtBachelor's or master's degree preferred in IT, business, or related field; 10+ years application or integration engineering, 5+ years management, ERP, integration architecture, API, ETL, CRM, vendor, Agile, and Scrum experience.
CelularityNASDAQ: CELU: Develops cell therapies and biomaterials derived from human placenta.
10+ YOEBachelor's in life sciences/engineering, 10+ years in QA/QC/regulatory in advanced therapeutics, GMP/GTP and FDA/EMA/GxP expertise, audit and inspection experience, leadership and cross-functional collaboration skills.
Madrigal PharmaceuticalsNASDAQ: MDGL: Develops and commercializes therapeutics for metabolic dysfunction-associated steatohepatitis.
15+ YOEBS in science/engineering,15+ years GMP QA/release experience with clinical supply,strong documentation and cross-functional coordination,inspection readiness,ability to travel 20-30% domestic and international.
Medical Director/Senior Medical Leader - Oncology Late Development - Prostate
Spring House, Pennsylvania, United States
$199k-$344k/yrHybridFull Time
Johnson & JohnsonNYSE: JNJ: Develops and manufactures pharmaceutical drugs and medical devices.
3+ YOEAdvanced medical degree, postdoctoral fellowship, and 3+ years of relevant urology or oncology clinical research experience; board-certified or board-eligible uro-oncologist or oncologist preferred.
Electronic Case Report Forms (eCRFs), Data Management, Biostatistics, Regulatory, Quality Management, Quality Assurance, Clinical Research Organization (CRO), NDA, MAA
Associate Director, Quality Assurance (Clinical Research Preferred)
Durham or Indianapolis or Wayne
$89k-$247k/yrRemoteFull Time
IQVIANYSE: IQV: Provides clinical research and healthcare data analytics services.
10+ YOE10+ years QA experience in pharmaceutical/biotech/CRO/clinical research, strong GxP/GCP knowledge, audit and CAPA experience, leadership, risk assessment, and Microsoft Office proficiency.
Johnson & JohnsonNYSE: JNJ: Provides pharmaceutical products and medical technology healthcare solutions.
7+ YOEBachelor's degree and 7+ years leading digital transformation, HR technology, automation, product management, or workforce experience initiatives. Requires AI strategy, cross-functional leadership, HR process, and global transformation expertise.