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The Part-Time Lab Technician will need to use formulation experience and scientific literature to develop, justify, and/or investigate formulation, processing techniques, and quality control protocols.
$15 - $17 an hourTemporaryExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reporting to the Executive Director of Development Quality Assurance, the Senior Director of Pharmacovigilance QA serves as a strategic partner managing quality and regulatory compliance related to Good Pharmacovigilance Practices (GVP) and other related activities performed by Drug Safety & Pharmacovigilance and Medical/Clinical Departments.
$200,000 - $280,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Our focus on combatting climate change through clean energy technology, our new net zero climate vision for 2030 and enhanced commitment to diversity, equity and inclusion; and supporting the communities we serve make this a particularly exciting time to join PSEG. Job Summary The Energy Management System (EMS) is a collection of specialized Electric Utility computer systems used by the Electric System Operations Center (ESOC) for the monitoring and control of PSE&G’s Bulk Electric System (BES.
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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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Packaging equipment, loading raw materials, equipment washing, quality control inspections and data recording. Interact with production team members, quality control and maintenance technicians to maximize output and efficiency.
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Quality Lab Analyst. Coordination with other brand protection associates and Quality with regards. Quality Lab Inspections. Sample Management (inventory management; check-in/check-out procedures; chain of custody.
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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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This includes documentation control, change control, deviation management, and CAPA (Corrective and Preventive Action) systems. 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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MedPro Healthcare Staffing , a Joint Commission-certified staffing agency, is seeking a quality MRI Tech for a contract with one of our top healthcare clients. Delivers quality, cost effective patient care in a professional manner.
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Coordinate Team Process Execution Excellence: Ensure that all warehouse processes are performed flawlessly by the team, maintaining high standards of accuracy and timeliness Develop and enforce SOPs, quality control measures, and performance metrics to drive execution excellence Facilitate regular team meetings to discuss process improvements, address challenges, and share standard methodologies.
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Supervise clinical staff to ensure all study activities are completed in accordance with applicable regulations and guidance, ICH, GCP and Bausch Health SOPs. Responsible for the quality of all study-related documentation (e.g., Trial Master File, site qualification and initiation visits reports, interim monitoring visit reports, clinical monitoring plan, informed consents, CRF completion guidelines, pharmacy manual, etc.
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Our client, a world-leading Pharmaceutical Company in Raritan, NJ is currently looking for a Packaging Quality Analyst to join their expanding team. Job Title: Packaging Quality Analyst / Pharma Industry / Hybrid Work.
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As a private Independent practice, Luxottica operates the optical dispensary while the Affiliated Doctor operates the Doctors office and provides high quality optometric care and service to patients.
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Works effectively to maintain an environment of excellence, which is patient focused, providing timely, compassionate, quality patient care. Key Words: MRI Tech, MRI Technician, MRI Technologist, Magnetic Resonance Technologist, Magnetic Resonance Imaging.
$2,850 a weekExpandApply NowActive JobUpdated Today
quality control jobs Title: quality control laboratory technician in Bridgewater, NJ
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