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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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Experience in the quality field on machined / mechanical parts using GD&T interpretation, able to use Optical Comparator and/or Vision Systems, exposure to CMM manual inspection, work with profilometers, thread gages / pin gages and various micrometers and caliper types.
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Quality Control Scientist - Microbiology, BioanalyticalPosition Summary:Catalent Pharma Solutions in Princeton, NJ is hiring a QC Scientist – Microbiology, Bio-Analytical and Raw Materials who is responsible for performing microbiological, bio-analytical and raw material testing to ensure the quality and safety of products.
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We are looking for a dedicated Construction Quality Control and Quality Assurance to join our talented team at our office located in Somerset, NJ.In this role, you will use your technical knowledge and skills to effectively train, supervise, communicate, execute, and manage the IPS Construction Quality Control and Quality Assurance (QA/QC) program for ongoing Construction Projects.
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The Behavioral Health Quality Management Supervisor shall report to the ABHNJ Quality Management Director and will work in close partnership with the ABHNJ Behavioral Health Medical Director, Behavioral Health Administrator, CMO, Behavioral Health Director of Network Relations and all matrixed growth partners to effectively manage access and quality of behavioral health benefits and care.
$40,600 - $89,300Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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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On-Board Services is hiring a Quality Control Chemist in New Brunswick, NJ! per hourLength of Assignment: year with a possibility of extension The Quality Control Chemist for the drug product testing team reports to the Finished Product/Stability Supervisor.
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The Chief Quality Officer will report directly into the EVP, Global Product Development & Supply Chain (GPS)with a dotted line reporting into the CEO and Chairman of the Board, and have responsibility for providing long-term Quality strategic insights connected to BMS business imperatives.
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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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Position requires on-site presence at companies' HQ Essential Duties and Responsibilities Conducting Training: Developing and conducting training programs for personnel on GMP and GDP requirements, quality systems, and relevant procedures to ensure understanding and compliance throughout the organization.
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Developing and Maintaining Quality Systems: Establishing and maintaining comprehensive quality systems in compliance with GMP and GDP regulations. Continuous Improvement Initiatives: Leading or participating in continuous improvement initiatives to enhance the effectiveness and efficiency of quality systems and processes, driving a culture of quality and excellence within the organization.
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Quality Risk Management: Implementing quality risk management processes to identify, assess, and mitigate risks to product quality, patient safety, and regulatory compliance throughout the product lifecycle.
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Managing Supplier and Vendor Quality: Assessing and approving suppliers and vendors based on their adherence to GMP and GDP standards. Reporting and Tracking: Providing internal customers with status reports, inspection results, improvement updates and other KPI and regulatory/quality required reporting.
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Title: quality Company: Direct Line Global in Belle Mead, NJ
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