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Certified Group includes Food Safety Net Services (FSNS), Certified Laboratories, EAS Consulting Group, Labstat International Inc., Advanced Botanical Consulting & Testing (ABC Testing Inc.), Microconsult Inc., and Micro Quality Labs Inc. Certified Group provides laboratory testing and regulatory consulting services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, tobacco, nicotine, cannabis, hemp, and other industries.
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2 Yeras experience entry writer or international transportation; knowledge of the Harmonized Tariff Schedule (HTS), Customs regulations, and PGA regulations related to FDA, CSPC, DOT, EPA, etc.
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Perform QC sampling and chemistry testing of raw materials under FDA/EU regulations, applicable International Regulations, processes and procedures to support GMP manufacturing. Working knowledge and experience with physiochemistry analytical methods such as HPLC, GC, TOC, FTIR/NIR/Raman, Karl Fischer, osmolality, melting point, optical rotation, and wet chemistry compendial methods.
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Participate in the I-SPY TRIALS, a ground-breaking national public-private collaboration among NCI, FDA, more than 20 cancer research centers, and major pharma, biotech companies as well as the University of California-wide Athena Breast Health Network, a learning system designed to integrate clinical care and research as it follows 150,000 women from screening through treatment and outcomes.
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Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures. Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures. We are currently looking for a Pathogen Lab Analyst to join our growing team.
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Export Administration Regulations (EAR)EU Dual use/Sanctions RegulationsForeign Trade Regulations (FTR)Office of Foreign Assets Control (OFAC)International Traffic in Arms Regulations (ITAR)US Customs and Border Protection (CBP.
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Maintain a current knowledge of applicable phase appropriate FDA and International cGMP regulations for Regenerative Medicine, Cell Therapy, and Good Tissue Practices. The Quality Assurance (QA) Auditor provides compliance and quality improvement support to the manufacture of phase 1/2a Investigational New Drug, Biologics manufacture and facility operations.
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Qc raw material analyst. Support QC sample management with the receipt of in-process samples and issuance of controlled documentation. skills: Quality control, HPLC, Quality Assurance, GMP (Good Manufacturing Practice.
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Deep understanding of the regulatory landscape for molecular diagnostics, including CLIA, CAP, FDA, and other international standards. This executive role is designed for a seasoned professional who combines deep technical expertise in molecular diagnostics with a proven track record of leading innovative R&D projects from conception to commercialization compatible with CLIA, CAP and FDA compliance.
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The duties include all tasks related to Customs clearance at the desk level, including Customs entry, clearance follow up with Customs & Border Protection (CBP), and other Partner Government Agencies (PGA), such as Food & Drug Administration (FDA), Consumer Product Safety Commission (CPSC), Department of Transportation (DOT), Environmental Protection Agency (EPA), and others as needed.
$17.35 - $49.73 an hourFull-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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NVE, Inc. provides Program Management, Administrative Services, Engineering, Facilities Management, and Security services to a range of Federal and local agencies including the US Department of State, US Agency for International Development (USAID), Nuclear Regulatory Commission (NRC), US Army, General Services Administration (GSA), US Food and Drug Administration (FDA), US Geological Survey (USGS), Department of Commerce, and Virginia Railway Express (VRE.
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Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc. Proficient in the use of several of the following laboratory instruments: Analytical Balance, pHmeter, automatic pipettes, FTIR, UV-Vis, Voltammeter, Autotitrator, HPLC, GC, IC, ICP, Flame AA, TOC,and Conductivity meter.
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Key areas of responsibility include: 1) ensuring compliance with US import regulations as outlined by Customs and Border Protection, FDA, FWS, FTC and other regulatory agencies as well as special trade programs including Foreign Trade Zones and CTPAT, 2) maintaining responsibility for TSA compliance as the companys designated coordinator, and, 3) working cross-functionally within the organization with the Domestic Customer Service, Audit, Solutions, and Finance departments.
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Ensure that testing meets international and domestic biocompatibility test requirements according to ISO, Good Laboratory Practices (GLP), FDA, EU MDR, Japan, and APAC countries. Ten or more years of biocompatibility of materials related experience including biomaterials, materials science, polymer chemistry and/or analytical chemistry.
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Maintain current knowledge of US and international regulations regarding Microbiology, Chemistry and cGMP's. Provide support for regulatory agency (i.e. FDA, HC, EU, TGA, etc.) Job Segment: Controls Engineer, QA Tester, Quality Engineer, Microbiology, QC, Engineering, Quality, Science.
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