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Interact with key site stakeholders, including but not limited to internal (Planning, Quality, Operations, Vein to Vein, Finance) and external (J&J, Avantor) to the department, on activities linked to his/her area of responsibilities.
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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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Job Title : Research Associate Quality Control. Research Associate Quality Control, Somerville, NJ. Demonstrate initiative to perform routine QC responsibilities such as sample coordination, lab equipment maintenance, QC document management, QC inventory control and reconciliation of sample requests/documents as needed.
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Maintain and control access to all facilities owned or operated, leased or owned by Hackensack Meridian Health. These responsibilities include but are not limited to continuous surveillance, reporting and documenting all incidents and remaining sensitive to the need for delivery of quality guest services and assistance to all persons visiting the Medical Center.
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What your duties will be: Drive new business with a focus on installation and service on large enterprise-sized Access Control, CCTV, Intrusion, Alarm and Low Voltage systems. What you'll experience: Brand partnerships at your disposal with the largest and most advanced systems - such as Lenel, Genetec, Honeywell Prowatch, Winpak, SH, S2, HID, Milestone, Avigilon, Verkada, EagleEye.
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Get paid an hourly rate of up to $55 as a Licensed Practical Nurse (LPN) in Edison, NJ (and nearby areas), with a completely flexible schedule that you control and the employee benefits that you deserve.
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Under the direction of the Youth Development Director, provides support of SACC, Camp and youth programs, to ensure all programs are of high quality and are member focused. Works with the director to ensure all school age child care programs, camp and enrichment programs including birthday parties for youth are of high quality.
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To deeply understand data quality, monitoring and validation needs and transform these insights into detailed business requirements for clinical data products. Craft study-specific Data Quality specifications and define key Clinical data metrics to uphold the highest data quality and integrity standards across study lifecycles.
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At PT Solutions, we’re more than colleagues; we’re a tight-knit community united in our mission to expand access to quality care. Twin Boro, a PT Solutions company, has provided New Jersey residents with the highest quality rehab services since 1980.
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Assessing the quality of management’s Business Process SOX control testing, and providing feedback to strengthen management’s testing capabilities. As a subject matter expert, you will partner with business leaders and play a central role in translating SOX compliance requirements into internal Verizon control guidance and enforcing a strong control environment.
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Working in close collaboration with its sister division, Population Health, Quality, and Implementation Science (PopQuIS), which houses ambulatory primary care pediatrics and our generalist research mission (Lawrence Kleinman, MD, MPH Division Director) the RWJMS Department of Pediatrics is moving its academic mission for general pediatrics to an exciting new trajectory.
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Must understand and apply cGMP requirements applicable to quality control laboratory. Perform testing using HPLC, UPLC, GC, IR, UV, Malvern Mastersizer, XRD, Dissolution, Karl-Fischer titrator, analytical balances, and other instruments as required.
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Enjoy competitive weekly pay between $2700 and $3200.
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The Team Lead for Authoring Support Group will be part of the Global Regulatory Operations group and will develop and manage the authoring support group within Regulatory Affairs (RA) to ensure timely and high-quality document delivery to the Regulatory Publishing Group.
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quality control jobs Title: field tech Company: Eaton in Bound Brook, NJ
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