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Familiarity with Good Documentation Practices (GDP), Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Ensure policies are followed regarding environmental health & safety, hazardous waste disposal and DEA compliance within the early development areas.
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Follows basic GMP, ISO Procedures, GLP, Safety, Lab Notebooks and/or other electronic records keeping tools. We're a cutting-edge innovator leading the way to a new future of plant-based consumer and industrial solutions to replace petroleum-based products.
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External Job Description:For more than a century, the people of Archer Daniels Midland Company (NYSE: ADM) have transformed crops into products that serve the vital needs of a growing world. With a global value chain that includes approximately 450 crop procurement locations, more than 330 food and feed ingredient manufacturing facilities, 62 innovation centers and the world's premier crop transportation network, we connect the harvest to the home, making products for food, animal feed, industrial and energy uses.
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1-3 years of QA or five years of GxP regulated (GLP, GMP, GCP) industry experience; 1-3 years of QA or five years of GxP regulated (GLP, GMP, GCP) industry experience; Discounts on local sports games, local fitness gyms and attractions Official Sponsor of FC Cincinnati.
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Ensures documentation meets facility audit as well as cGMP or GLP requirements. Background in HPLC and other analytical techniques (GC, AA, UV, TLC, and wet chemistry) desirable. Fresenius Kabi is an Equal Opportunity/Affirmative Action employer.
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Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP.
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With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
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Follow basic GLP, GMP, and Safety standards. QC technician responsible for quality analysis of raw materials, finished products, expired materials, and Contract Manufactured items. This position reports to the QC Manager.
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With industry-advancing innovations, a complete portfolio of ingredients and solutions to meet any taste, and a commitment to sustainability, we give customers an edge in solving the nutritional challenges of today and tomorrow.
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Follows basic GMP, ISO Procedures, GLP, Safety, Lab Notebooks and/or other electronic record keeping tools. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law.
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Microsoft word, gmp, sop, data entry, sample preparation, sample collection, biology, glp, inventory. Provides support to Sample Coordinator and performs administrative tasks in the Sample Management department.
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Responsibilities:Responsible for GLP, including equipment monitoring and calibration as well as media preparation and biohazard disposalEvaluate, develop, implement, and maintain testing procedures and programs.
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For more information regarding our efforts to advance Diversity, Equity, Inclusion & Belonging, please visit our website here: Diversity, Equity and Inclusion | ADM. ( Maintain QC laboratory, stocking/purchasing supplies and raw materials.
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Work in accordance with all relevant requirements including, but not limitedto GMP, AIB, OSHA, HACCP, FDA, USDA, GLP and internal safety guidelines. Work in accordance with all relevant requirements including, but not limitedto GMP, AIB, OSHA, HACCP, FDA, USDA, GLP and internal safety guidelines.
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Our client is seeking a Microbiologist for their manufacturing facility in central Illinois. MUST have PCR experience and proficiency interpreting results. MUST have a B.S. in Microbiology or a related degree.
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glp job in Cincinnati, OH
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