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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.
$1 - $2ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Knowledge of cGMP/GDP regulations, ICH Guidelines, and CMC (Chemistry and Manufacturing Controls) recommended. This includes documentation control, change control, deviation management, and CAPA (Corrective and Preventive Action) systems.
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Responsibilities Ensure compliance with cGMP, Quality Systems Regulations, WIs, SOPs, and Health & Safety Requirements. Familiar with inventory control using RF scanner. Responsibilities Ensure compliance with cGMP, Quality Systems Regulations, WIs, SOPs, and Health & Safety Requirements.
$18 - $22 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Intermediate knowledge of Microsoft Word, Microsoft Excel and Adobe AcrobatKnowledge of cGMP/GDP regulations, ICH Guidelines, and CMC (Chemistry and Manufacturing Controls) recommendedExcellent communication, organizational, interpersonal and computer skillsExcellent Oral/Written Communication SkillsDemonstrated ability to manage multiple competing prioritiesSolid organizational skills and attention to detail.
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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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Experienced in cGMP aseptic manufacturing environments, preferably in production, quality control or quality assurance. Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
$97,750 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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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.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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In coordination with the Associate Director, QMS, primary areas of responsibility include QA review and approval of Deviations/CAPAs/ECs, QA review and approval of Quality Documents in the Document Control System, tracking and trending.
$97,200 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Experience working across Supply chain, PM, Manufacturing, Quality Control in a cGMP environment within Biologics or Cell Therapy Operations. Experience working across Supply chain, PM, Manufacturing, Quality Control in a cGMP environment within Biologics or Cell Therapy Operations.
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Perform duties associated with synthesis, quality control, and quality assurance of FDG and NaF including reagent preparation. Provide on-the-floor QA oversight of manufacturing, QC, and other cGMP activities.
$116,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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As a Biologist, you will play a crucial role in ensuring quality control within our laboratory environment. This position requires a strong background in biology or biochemistry, with a focus on adhering to cGMP regulations while working both independently and collaboratively.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Experience working across with Supply chain, PM, Manufacturing, Quality Control in a cGMP environment within. Biologics or Cell Therapy Operations. The On-Board Family of Companies conducts operations through its Corporate Headquarters located in East Windsor, NJ along with Regional Offices in New Castle, DE and Wake Forest, NC. On-Board’s Mission is to provide “Flexible Service by applying the talents of our people, work processes and technology to meet our clients’ expectations in a Safe, Responsible and Dependable manner.
$114 an hourFull-timeExpandApply NowActive JobUpdated 4 months ago - UpvoteDownvoteShare Job
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Self starter and team player, Analytical, leadership, strong communication, stakeholder management and time. Minimum 6 years of Supply chain planning along with Project Management experience. Experience with root cause analysis, change management and material lifecycle management.
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Health Canada cGMP, European MDD and MDR. as a compliance SME Act as independent reviewer on design control projects to ensure compliance with internal procedures and external standards and regulations.
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