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Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality Control Analyst, CAR-T Critical Reagents (1 of 4)! The Quality Control (QC) Analyst is responsible for preparing and conducting testing of critical reagents used by the QC laboratories.
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The Area Chief of Staff partners with the Practice Manager (if applicable) to drive the culture and delivery of quality care by the veterinary provider team (DVM, CVT, VA) in their assigned hospitals to ensure that every pet receives consistent care aligning with our six domains of quality(safe, effective, patient/client centered, timely, efficient and equitable care.
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The Clinical Systems Analyst will assist the Senior Director of Clinical and Development Systems in planning, directing, and coordinating software projects and support activities within the Drug Safety, Pharmacovigilance, Regulatory, Clinical Operations, and Quality Assurance groups.
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Experience working with data management projects having experience in data analysis, data governance, data quality and lineage. Experience with any of the following is a plus: Quantum, Swift, Aladdin, Clearwater, Chatham Financials, Pinnacle, QRM.
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Join our Digital Quality team as Digital Risk and Compliance Lead and make it happen. Critical aspect of the role includes defining an agile quality and compliance strategy that supports Digital Data unit in their effort to establish a standardized, resilient, and sustainable data pipeline - including data sources, data quality, data governance, data management and master data management.
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We specialize in aluminum extrusion and fabrication, and we’re committed to delivering high-quality products through continuous improvement and advanced manufacturing techniques. The successful candidate will leverage Lean Principles, Six Sigma Methodologies, and Advanced Automation and Robotics to drive continuous improvement, enhance product quality, and increase operational efficiency.
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The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. A background of pharmaceutical manufacturing or quality control/quality assurance is a plus.
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3-5 years of experience in drug safety, pharmacovigilance, quality assurance, or a related field. Provide drug safety and pharmacovigilance leadership to the quality and compliance team, fostering a culture of collaboration, excellence, and continuous learning.
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Manufacturing quality technician. Employee is responsible to follow and uphold all Food Safety, Food Quality, Occupational Safety, Health and Environment policies and procedures as pertains to role.
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Attention to detail and familiarity with batch record review process and FDA quality standards. Hands on experience with quality systems in a regulated environment, including change control, CAPA and investigations.
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Knowledge and understanding of drug development including regulatory requirements and quality standards applicable to nonclinical and clinical laboratories (e.g., GLP, GCP, ISO). They will also collaborate with internal stakeholders to develop and implement effective outsourcing strategies and implement vendor oversight frameworks to ensure quality and performance.
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We are seeking a Warehouse Manager to oversee the operations of a 3PL distribution warehouse, kitting, and assembly facility in Branchburg, NJ. This role encompasses managing material receipt, inventory control, order processing, outbound shipping, quality control, kitting project assembly, and additional value-added services.
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The RN PACU provides safe, effective, and quality patient-family centered care in the perioperative services for all patient populations. Job Summary: The RN PACU is a Registered Nurse that provides quality patient care using the nursing process, the medical plan of care, and organizational policies.
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Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting a Supervisor of Quality Systems Investigations, CAR-T in Raritan, NJ! Experience in Quality Assurance/ Quality Systems related to cell therapy manufacturing in commercial setting.
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Experience with Veeva (Quality Docs, QMS and Training modules) a plus. Global Pharmaceutical company, with US HQ in Central New Jersey, focused in Metabolics, Endocrinology and Oncology is expandingLooking for a strong Quality Assurance Manager for the entire North American manufacturing and quality organization.
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quality job in Branchburg, NJ
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