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Must have sufficient experience and a demonstrated knowledge and understanding of global safety reporting regulations and guidelines including the FDA, ICH, & EU Regulations and Requirements for Pharmacovigilance.
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Preferred 10 years’ experience in regulatory & scientific affairs focused on ingredient issues management in food products and packaging and/or related product categories (such as food supplements, cosmetics) with proficiency in regulatory affairs and compliance.
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Primary responsibility is to complete documentation and analytical testing of raw materials, in-process materials, stability samples, finished products and product development in a timely manner, while maintaining compliance with cGMP requirements, FDA, OSHA, EPA, and DEA.
Full-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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They act as the management representative for Quality and Animal Food Safety domains, ensuring customer satisfaction, adherence to legal regulations, and continuous improvement of systems and processes to guarantee product safety, legality, and quality.
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Gene Delivery Product and Analytical Development (GDPAD) leadership seeks applicants for the Product and Analytical Lead role to drive strategy, knowledge, and deliverables related to lentiviral, AAV vector analytics development that are required for CMC milestone achievement of clinical program.
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Demonstrated method development experience in techniques such as viral safety and potency assays, viral titer assays, quantitative PCR (qPCR), ddPCR, NGS, ELISA, etc. This is a highly visible role that will serve as the GDPAD single point of contact for program vector analytics strategy, for CMOs/CTLs, and across our partner organizations (Process Sciences & Technology, Drug Product Development; Product and Analytical Development, Quality, Regulatory, Program teams.
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Partnership with the following stakeholders will enable the Quality Engineer to be successful in this role: Purchasing, Operations, Shipping, Receiving, Corporate Product Stewardship, Corporate Quality, Safety, Maintenance, Human Resources, and Operations Senior Leadership.
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Report to Administrator any site visits and/or communication from OSHA (Occupational Safety and Health Administration) and CPSC (Consumer Product Safety Commission) Fire/Building/City/Town/Local inspector.
$16 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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High Hotels Ltd., is a leading operator of select-service and extended stay hotels across PA & NJ. We strive to maintain the highest standards in guest service and overall product quality. As a Night Auditor , you will be responsible for positively representing the hotel to our guests by responding courteously and efficiently to guest inquiries and requests, acting as a source of information about the hotel and surrounding area, assisting with arrivals and departures, and maintaining the safety and security of the hotel guests and co-workers.
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Knowledge of modern CAD tools including but not limited to: MasterCAM, SolidWorks, ProE, and AutoCAD. Experience handling in the fabrication of an entire project from drawings to finished product.
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Work with Process and Analytical Development (P&AD) departments and cross functional partners to build vector process and product understanding that serves as the foundation of the analytical strategy including establishing and iterating QTPP, CQAs, and specifications throughout development.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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By working closely with end-users and grinding expert partners, Saint-Gobain Abrasives designs and provides customized solutions to secure the best option for performance, cost and safety. Time will be spent demonstrating and facilitating training on the proper application and use of all products in Saint-Gobain’s product portfolio.
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Ensure that all safety measures are consistent with Salvation Army policy and Government regulations and all personnel are in compliancMaintain regular communication with immediate supervisor and Store Managers, Sorting Room Supervisor, Administration office and the Administrator, as required, on matters pertaining to warehouse operation and personnel within production operatioEnsure that all equipment (communications, keys, material handling, etc.
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Additional Info: Monday 5 AM - 3:30 PM, Tuesday - Friday 4 AM - 3:30 PM Yard Jockey for extremely busy Marlborough, MA. Occasionally shuttling product from Southborough location to Marlboro. Your safety is our top priority, and we comply with DOT and FMCSA. Join the TransForce team.
$45,000 - $100,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Processing experience includes but not limited to: Chromatography, writing/using unicorn methods, Tangential Flow Filtration, Aseptic processing, bulk drug substance and drug product operations.
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product safety jobs in Titusville, NJ
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