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In-depth knowledge of State and Federal rules/regulations such as EEO, OSHA, FDA, USDA. The Area Production Manager assists with the supervision of the planning, organizing and directing of production activities and employee placement/training/development to cost effectively produce a high quality finished product.
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Knowledge of ICH guidelines, FDA Drug Regulations with respect to DDMAC, PhRMA Principles on Conduct of Clinical Trials and Communication of Clinical Trial Results, and OIG Compliance Program Guidance for Pharmaceutical Manufacturers.
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Assist and partner with business leaders on implementation of process improvement (Six Sigma / Lean/ Kraft Heinz Management System (KHMS), including leading change initiatives, planning, and facilitation.
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Maintain and adhere to provisions of FDA, OSHA, GMP, and ISO specifications Review and monitor project progress, quality, and safety. LEED AP, PMP, and/or CCM designation(s) preferred. About the role The purpose of this position is to lead individual, multi-disciplined real estate construction and renovation project solutions for life science client, with direct accountability for project delivery.
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Our portfolio includes projects within multiple markets sectors including: FDA Regulated/Food & Beverage, Advanced Manufacturing, Mission Critical, Mobility and Energy. Collect and provide research, forecasts, and trends of the industry to assist the Executive Vice President (EVP) during the development of the annual strategic marketing and business planning process.
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Thorough knowledge of ISO/FDA regulatory requirements. Thorough knowledge of ISO/FDA regulatory requirements. 4-6 years years industry experience working in medical device and/or pharmaceutical manufacturing, Quality Assurance or Regulatory fields.
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Support compliance with external and internal regulations, such as International Standards Organization (ISO) and Food and Drug Administration (FDA) regulatory compliance, and Johnson & Johnson (J&J) requirements.
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Familiarity with regulatory standards (FDA, EPA, OSHA) related to chemical production. Familiarity with regulatory standards (FDA, EPA, OSHA) related to chemical production. Skills: - Bachelor's degree in Chemistry, Chemical Engineering, or a related field (or 5+ Years experience.
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Performs phlebotomy and collection procedures and processes related to the collection of blood and/or blood components from donors according to the organizations policies and procedures, the Food and Drug Administration (FDA) regulations, and American Association of Blood Banks (AABB) standards.
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We are seeking a Medical Science Liaison (MSL), field-based scientific/clinical expert that will report to a Regional Director of MSLs within the Medical Affairs (MA) department. The MSL is responsible for identifying, developing, and managing relationships with current and future Healthcare Providers (HCPs) in academic and community practices.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Overseeing development new products ensuring product quality meets expected standard set by regulatory bodies i.e., FDA requirements. Building robust relationships between cross-functional teams from procurement down stream until order fulfillment.
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Coordinate the preparation of regulatory documents for submission to Institutional Review Board (IRB), other internal committees, and the FDA as necessary (Submissions include but not limited to: Initial study submission, Continuing Review Reports, Amendments and addendums to protocols, Informed Consents, Drug Brochures, Advertisements.
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Working knowledge of related regulatory, oversight, and advisory agencies: AIB, FDA, USDA, EPA, PMO, 3A, GMPs, SPS, SSOP, and HACCP. Practical experience in some of the following: baking, thermal processing, commercial heat exchangers, fluid transfer (fittings, valves, pumps), evaporation, sterilization, CIP, SIP, and systems automation/integration in both consumer and bulk food processing.
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Blood banking experience, management experience, or FDA regulatory experience desired. Blood banking experience, management experience, or FDA regulatory experience desired. LifeSouth is a non-profit community blood bank serving more than 125 hospitals in Alabama, Florida, and Georgia.
$82,500 - $90,750 a yearFull-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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3+ years of experience in a food or FDA regulated manufacturing facility. Our client is currently seeking a Sanitation Manager in Central Florida. Bilingual Spanish skills are a plusSolid compensation package, including great benefits, relocation assistance and this is a 1st Shift Position.
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fda job in Jacksonville, FL
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