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The Quality Assurance Document Control Specialist role is an exempt position responsible for supporting the document management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.
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Manages the packaging Batch Record review and approval process with Quality Assurance and other CSO personnel. Works closely with Quality Assurance to obtain temperature excursion disposition to update impacted inventory in IRT and other related systems.
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Reporting directly to the Senior Manager of Quality, this position collaborates closely with External Manufacturing Organizations (EMO), spanning pharmaceuticals, medical devices/combination products, consumer products/OTC, and biologics sectors, ensuring adherence to cGMP regulations and Bausch Health requirements.
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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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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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Functions and activities include Disposition activities, including incoming materials and final drug product, QA shop floor oversight of manufacturing operations, Quality Assurance review and approval functions, and QC laboratory oversight, among others.
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Support Quality Systems such as; change control, deviation, CAPA, audits, quality metrics, etc. This role will be a hands-on resource reporting to the Quality Control Manager. We are seeking an innovative, creative, and detail-oriented Senior Quality Control Analyst to join our team in Bridgewater, New Jersey.
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Lead risk assessment, quality assurance, quality/validation strategy definition and oversee their execution in collaboration with external service providers. Join our Digital Quality team as Digital Risk and Compliance Lead and make it happen.
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Must have experience collaborating with other teams such as Regulatory Affairs, Clinical Development, Quality Assurance, Legal, Clinical Operations, etc. The successful candidate will provide quality expertise to manage and improve processes across Aquestive's development program, ensuring compliance with Good Clinical Practices (GCP), Good Laboratory Practice (GLP), Preclinical stage and GMP for clinical manufacturing oversight.
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In addition, this role will perform critical quality assurance activities such as Change Management, SOP Management, and Audit oversight. Experience with Veeva (Quality Docs, QMS and Training modules) a plus.
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Use Mastercam CAD/CAM software to define efficient tooling operations to create high quality parts. The CNC Machinist Programmer will be responsible for operating several CNC machining tools to produce a variety of precision parts to support our growing sales of industrial drying equipment and systems.
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As an Appliance Repair Technician, you are the key component in providing excellent customer service by providing high-quality maintenance services for our customer's appliances. Quality of Work: This role requires critical thinking skills and the ability to problem solve.
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Johnson & Johnson is currently recruiting for a Senior Principal Scientist, Global Commercial Data Science (GCDS) , J&J Innovative Medicine. Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
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Utilize your extensive master data expertise to demonstrate a profound understanding of SAP MDG Materials, BOM, Recipes, MRP, MPS, Work Centers, Batch Management, Quality Inspection, Costing among others.
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A background of pharmaceutical manufacturing or quality control/quality assurance is a plus. Works closely with quality, manufacturing, Global Regulatory Affairs (GRA), and technical staff from global locations within industrial network, contract manufacturing organizations (CMOs), and alliance partners to author high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers.
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quality assurance jobs Company: Johnson in Bedminster, NJ
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