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In person or Remote (East Coast with initial training onsite at Bridgewater, NJ and few days for the first few months)DutiesThe CMC Regulatory Technical Writer II authors high quality Module and regulatory submissions for both development and post-approval dossiers, change controls and technical reports.
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Coordinating internal pre/post-production efforts Keeping detailed records of all findings, communications, and settlement agreements. Urgently Hiring We're in need of a Claims Adjuster at Northeast Power Dry, Xactimate is a plus.
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Pre-sales and post-sales technical support of spectroscopic products. A leader in Raman spectroscopy, HORIBA’s New Jersey Optical Spectroscopy Center specializes in scientific instruments and has an opening for a Raman Applications Scientist.
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Position Status Full Time Posting Number 24FA0689 Posting Open Date 06/27/2024 Posting Close Date 07/26/2024 Qualifications Minimum Education and Experience Terminal degree in the biological sciences (e.g., PhD, DSc), plus at least 5 years’ experience post-degree; or terminal professional degree in the medical or veterinary sciences plus at least 10 years’ experience post-degree.
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There is employee ownership to meet community post-acute, long-term care and senior living needs sparking innovation, creativity and collaboration. Create and implement education programs in response to identified infection control needs identified through QAPI, rounding, center quality measures, or other means.
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Identify exceptions that require post-closing follow-up. Post funding complete the booking sheet in accordance with timeframes in the booking procedure. Experience with basic office programs and equipment including Microsoft Office.
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Prepare for post-production support for all lines of business in ClaimCenter. In addition, this role will assume post-production responsibilities for our ClaimCenter implementation. Longer term, this role may expand as needed to support further business-sponsored projects targeted at improving efficiencies/workflow or adhering to compliance regulations for the various lines of business we write.
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Be available for early Saturday morning post-production business testing after releases, which occur every 3-4 weeks. Familiarity with Duckcreek or other Chubb systems or applications (Marketplace, BCWS, Genius, WIP, BizTalk, etc.
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Job Summary:The CMC Regulatory Technical Writer authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports.
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The Project Manager will be responsible for overall project implementation for lifecycle management and post-approval changes for Bausch + Lomb portfolio of products with a focus on geographic expansion of existing products into new markets.
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3 years' post-graduate experience in human immunology, virology or lentivector gene therapy, 2-3 years of industry experience is preferred, in vivo CART experience is a plus. Develop cell therapy gene editing platform and optimize cell-based immunoassays, including virus packaging, immune cell isolation and expansion, multi-color flow cytometry, ELISA, cytotoxic assays.
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The Director, Clinical Safety, will be a product safety lead or part of a product safety team, and be responsible for overall product safety strategy or specific areas of safety surveillance and risk management, and provide safety leadership including but not limited to clinical studies, post-marketing surveillance, signal detection and management, important safety topics, and regulatory submissions.
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Provided programming support on ISS/ISE and post-submission activities. Works with Statistician and Statistical programmer to assure results are consistent with expectations, and quality control (QC) procedures are.
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The Research Compliance Auditor is a key contributor to HMH’s Research Compliance Audit and Monitoring Program (RCAMP) which is responsible for post-approval review and auditing of Hackensack Meridian Health Research portfolio for compliance with applicable policies, regulations, and best practices.
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5-10 years post degree, ideally in cryogenic related field. Technical support for Otis location. 5-10 years post degree, ideally in cryogenic related field. Safety in transfill network and at Otis.
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post job Title: sponsored programs in Bridgewater, NJ
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