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The right candidate must be familiar with pharmaceutical or related manufacturing processes and be thoroughly familiar with GMP/cGMP regulations (e.g. FDA cGMPs, ICH, IPEC, etc. SQA manages Supplier Audit and Supplier Development programs for customers in many industries including Pharmaceutical, Medical Device, Automotive, Aerospace, and Electronics manufacturing.
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Minimum of 5 years comprehensive food processing, food safety and quality experience with an extensive background in manufacturing food industry, HACCP, USDA, or FDA preferred. The Quality Assurance (QA) Supervisor has the primary responsibility for protecting the food by supervising QA Technicians to effectively implement food safety and quality procedures and meeting all regulatory, customer, and GREAT KITCHENS FOOD COMPANY requirements.
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KNOWLEDGE SKILLS & ABILITIES:Extensive knowledge of OSHA regulations, Joint Commission and HFAP and CMS COP standards, FDA and other applicable State and Federal rules and regulations. GENERAL SUMMARY/BASIC PURPOSE OF JOB:Reporting directly to the President of Mount Sinai Hospital Medical Center, the Vice President, Facility Operations, Design & Construction, and Real Estate develops and executes a system wide plan for Facilities Management which results in operational excellence, high customer and staff satisfaction, consistent and effective service delivery, and improved operating costs.
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Learn and maintain thorough familiarity and compliance with all state and federal regulations, U.S. Food and Drug Administration (FDA)-approved Standard Operating Procedure Manual, Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice (cGMP) and internal company procedures.
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As a Sanitation Manager, you will be responsible for maintaining a clean and safe working environment for all employees, adhering to industry sanitation standards, and ensuring compliance with FDA, SQF, HACCP, FSMA, and GMP standards.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Facilitate the investigation and resolution of intensified plant issues including quality holds, priority consumer complaints, and FDA/USDA regulatory matters. Good knowledge of statistics and statistical process control (SPC)( Six Sigma Green Belt experience preferred.
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Be the point person at the site for regulatory inspections (FDA/CFIA), identify preserved (ie, Organic, Kosher, ) and customer audits. Quality Manager is required to have or complete PCQI training.
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Write, test, and implement programs using JDE EnterpriseOne Tools (RDA, FDA) and other supported toolsets, including EDI. Write, test, and implement programs using JDE EnterpriseOne Tools (RDA, FDA) and other supported toolsets, including EDI.
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Ensures compliance with FDA and other relevant regulatory requirements and standards Ensure department personnel are aware of Fresenius Kabi's Environmental and Energy Management System including Environmental and Energy Policy.
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Job Summary The Validation Manager is responsible for managing Validation personnel at Melrose Park facility. Provide technical expertise and oversight on various technical documents (MBR's, New Product Validation Reports, MCR's, etc.
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Working knowledge of FDA regulations, Good Manufacturing Practices (GMPs), HACCP, food allergens and pest control. Demonstrated knowledge and application of statistical process control, quality assurance techniques and tools and quality management principles in a food, chemical or pharmaceutical manufacturing environment.
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Provide a source of advice on FDA regulatory requirements. Solid understanding of FDA regulations and quality systems pertaining to contract research supporting Pharmaceutical industry and good documentation practices within the CRO, life sciences, or pharmaceutical industries.
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We are seeking a Part time Contract Physician who will be responsible for ensuring donor suitability, product integrity, and the continued good health of donors through compliance with FDA regulations and our Donor Center SOP. You will not be seeing patients in this role, you will primarily be quality checking work and information and signing off on that.
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A hybrid schedule , with 2 days of remote work (Tuesday and Thursday) and 3 days on-site (Monday, Wednesday, and Friday), blending the convenience of working from home with the benefits of in-person collaboration.
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Support the implementation of new and existing FDA and OIG guidance documents, emerging state and federal regulations, and industry codes to current policies, training and monitoring activities as they relate to business activities and communications with healthcare professionals and/or patients or patient advocacy organization.
$115,000 - $130,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago
fda job in Bedford Park, IL
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