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Reviewing control panel wiring diagrams. Experience interfacing various control systems to OPC Server applications and communication tto other control systems via OPC. Knowledge of general purpose OPC Server applications from Matrikon or OSI PI is desirable.
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This role will be a hands-on resource reporting to the Quality Control Manager. Support Quality Systems such as; change control, deviation, CAPA, audits, quality metrics, etc.
$90,000 - $210,000 a yearFull-timeExpandApply NowActive JobUpdated Today - 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.
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Drive project governance utilizing project Leadership and resource management with PVH PMO tools and processes. In addition to complying with all applicable laws, PVH also has a strong corporate commitment to inclusion, diversity and to ensuring that all current and future PVH associates are compensated solely on job-related factors such as skill, ability, educational background, work quality, experience and potential.
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Must maintain and apply working knowledge of PSEG Standards for Business Controls and NERC CIP requirements (North American Electric Reliability Corporation Critical Infrastructure Protection.
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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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We are seeking an innovative and highly motivated Senior Manager, Quality Operations, who will contribute significantly to the growth of the Cellares team. 10+ years of experience in a GMP environment in pharmaceutical, biologics, vaccines, cell or gene therapy operations, including solid experience in Quality Systems and Regulatory CMC.
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The Director, Quality Operations Head, Raritan Cell Therapy Manufacturing Operations leads and handles all aspects of Quality Operations in support of the Raritan CAR T manufacturing site, in full compliance with established cGMP, J&J and JSC requirements.
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The Digital Quality Lead will provide key quality expertise to establish pragmatic compliance controls supporting selection of data platforms, establishment of global data architecture, implementation of data governance tools at scale, enabling data science capabilities, and responsible design/development/deployment and use of AI enabled solutions.
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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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The Senior Software Engineer will support Research, Discovery and Development activities and leverage DevSecOps toolkits such as GitLab SaaS version control software, Terraform, Cloud Formation, to ensure smooth and secure delivery of R&D Digital Products, build and deploy scalable and resilient applications.
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Optimize usage maximizing utilization of deployed resources and reduce spend leveraging cost management tooling. An SRE is required to adhere to all Enterprise processes and controls (i.e.: ChgMgt, Incident and Problem Mgmt., etc.
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Perform high quality and consecutive professional eyelash extension services. Perform high quality and consecutive professional eyelash extension services. 1+ years as a Lash Stylist required. The Lash Lounge is the premier salon for Lash Extensions with over 100 locations in the United States.
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The role will provide scientific and strategic guidance to global project teams and will oversee the internal and CRO resources as they relate to TBS. Responsibilities Lead projects, provide oversight of outsourced GxP bioanalytical validations and sample analysis from early to late development for pharmacokinetic and biomarkers studies.
$140,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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 control project controls cost jobs Title: project manager cost in Branchburg, NJ
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