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Over 5 years in a technical or senior management role within food manufacturing, preferably in the meat and/or poultry processing industry, with experience managing HACCP and SQF programs. Extensive knowledge and experience in developing and managing HACCP, Preventative Controls, GMP, SSOP, SQF, BRC, and customer-driven quality and food safety programs.
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Working knowledge of laboratory GMP, quality, compliance and data integrity requirements and related recent industry trends. Working knowledge of laboratory GMP, quality, compliance and data integrity requirements and related recent industry trends.
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Coordinate international sales, including facilitating transactions, accounts receivable and ensuring compliance with international regulations for export shipment. Additionally, the ISR is responsible for managing requests for products, price and technical information.
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This position requires independent execution of SOX compliance controls testing, operational and financial assurance and advisory activities. Today, we have more than 3,500 employees across 28 different locations, with a family of brands that also includes SuperATV and Dayton Parts.
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Knowledge and experience in implementing sales, account management, and new business development strategies; managing product rationalization projects; system process improvement; metrics creation; and sales incentive compensation programs is required.
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Yoh has an exciting, full-time opportunity for a Survey Crew Chief to oversee survey operations for our Civil Engineering client. The ideal candidate will have 5+ years of overall surveying experience, prior experience as a Crew Chief, and live within a commutable distance to the office in Chalfont, PA for an onsite environment.
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Compliance Management International (CMI) is a premier global provider of environmental, health, and safety (EHS) services, serving clients of all sizes for over 25 years. Compliance Management International (CMI), is an equal opportunity employer, considering all applicants without regard to race, color, religion, gender, sexual orientation, age, national origin, disability, veteran status, or any other protected status.
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Collaborate with cross-functional colleagues across multiple departments such as Legal, Privacy, Compliance, Procurement, Drug Safety Unit, Brand Teams, Medical, Regulatory, Specialty National Account Directors, SAS Operations, SAS Data Analytics, USMA Access Leads, Payer Brand Marketers, Field-based Representatives, Trade, Digital and SPP customers.
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In compliance with OSHA standards, operate equipment (stand up forklifts, stand up staddle trucks, walk behinds, single/double pallet jacks and RF) in a manner that promotes safety. Under general supervision, Lift Truck Operator (LTO), Warehouse Worker will ensure safe and accurate receipt, storage, and shipment of food products utilizing equipment including, but not limited to sit down and stand up forklifts, stand up straddle trucks, walk behinds, pallet jacks, double pallet jacks and radio frequency equipment.
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The MDS Coordinator - RN is responsible for the timely and accurate completion of the MDS treatment assessment tool and for reviewing care plans and their delivery for factors specific to our patients/residents such as physical, cognitive, and socialization factors to ensure compliance with our high standards of care.
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Experience managing contracts incorporating Industrial Automation and Motion Control Technologies. Taking end-to-end responsibility for technical solutions, financial results, schedules, customer satisfaction, compliance and Environmental Health and Safety.
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Support Material Compliance and GT's regulatory status through maintenance of our chemical substances and raw materials information utilizing the SAP EHS module. May be responsible for data entry or checking accuracy of data input by others to ensure proper work flow, approvals, and/or compliance requirements.
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The Quality Assurance Laboratory Specialist is responsible for providing Quality direction and oversight to WP Laboratory Operations in the management of those areas assigned, such as Internal Auditing, Training, Change Control, Inspection Management, Documentation, Deviation Management and Risk Management in order to maintain compliance with Regulatory requirements.
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Experience managing sample chain of custody within a GLP/GMP lab. Strong knowledge in GxP and compliance guidelines, preferably in a bioanalytical laboratory environment. Job Description: Maintain and manage inventory of GLP and Clinical bioanalytical samples and critical reagents.
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Works in compliance with all regulatory standards including EH&S, cGMP, Radiation Safety, applicable pharmacy laws, DOT, and internal policies and interpretations of the above as required. It is SiemensHealthineers’ policy to comply fully and completely with all United Statesexport control laws and regulations, including those implemented by theDepartment of Commerce through the Export Administration Regulations (EAR), bythe Department of State through the International Traffic in Arms Regulations(ITAR), and by the Treasury Department through the Office of Foreign AssetsControl (OFAC) sanctions regulations.
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