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Ensures compliance with regard to U.S. Government regulatory agencies such as FDA, EPA, FCC, Fish & Wildlife, etc. The Account Representative - Customs Brokerage is responsible for coordinating and executing shipments to ensure adequate service levels of clients are met.
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Design, Mechanical, Solidworks, Gd&t, New product development, Electromechanical, sub assembly, Medical device, FDA, iso13485. Design, Mechanical, Solidworks, Gd&t, New product development, Electromechanical, sub assembly, Medical device, FDA, iso13485.
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Ensure compliance to all applicable FDA, ISO, Luminex Quality System, and safety requirements. 10 Years Manufacturing operations leadership experience 3 Years Experience in FDA regulated industry and/or ISO certified organization.
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Communicates with specified offices, departments, and teams on all issues affecting customs brokerage. Minimum 3 years experience in customs brokerage or an equivalent combination of both education and experience.
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In-house counsel experience in the field of biotechnology/pharmaceutical research and development and its related FDA regulations is preferred. Our flagship product PROVENGE (sipuleucel-T), was the first FDA approved immunotherapy for the treatment of metastatic castrate resistant prostate cancer and is made from the patient's own immune cells.
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Direct acquisition and analysis of laboratory research data following GCP and FDA regulations. The Lundquist Institute offers a variety of investment options through Fidelity Investment, TIAA/CREF.
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Execute and enforce Food Safety, HACCP, FDA, and labeling policies to guarantee compliance with industry standards. HACCP is required, PCQI Preferred. The QA Team Supervisor will report to the QA Manager and be responsible for overseeing the Quality Assurance team, ensuring compliance with all relevant regulations, and maintaining the highest standards for our products and processes.
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We are academically affiliated with the David Geffen School of Medicine at UCLA and work in partnership with the Harbor-UCLA Medical Center. Previous work experience as a study coordinator working on a clinical trial.
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Must adhere rigidly to all GMP policies and procedures as stipulated by the FDA. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives.
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Experience with inventory policies and procedures (Including USDA, FDA, and International Policies). You’ll take the lead in defect tracking and remediation processes, analyzing root causes, and charting the optimum path forward.
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Communicate with the FDA Project Coordinator and local supervisor to maintain the warehouse sampling schedule. Digitally transmit photographs in appropriate quality to the FDA Project Coordinator using various service providers as directed (Google Drive, Dropbox, Box, etc.
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Batching and Filling: Execute batching and filling operations in GMP/FDA regulated environments, handling bulk product batches ranging from small-scale to large-scale production. Batching and Filling: Execute batching and filling operations in GMP/FDA regulated environments, handling bulk product batches ranging from small-scale to large-scale production.
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Generally, you are considered fully vaccinated 14 days after receiving the last dose, as recommended by the manufacturer, of a vaccine that has been authorized by the FDA for use in the United States, including vaccinations that have been approved pursuant to an Emergency Use Authorization.
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Completes all forms (i.e., labs, tissue, FDA, billing, waiver of liability for visitors) and logs (i.e., tissue, Lens, temperature/humidity) as appropriate. Receives brief report from Pre op RN when the patient is taken to the OR, Assists anesthesiologist in transfer of patient to and from OR, Brings chart and any supplies needed for the patient after discharge to the PACU, Gives brief report to PACU RN when taking the patient from the OR to PACU.
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The Animal Health Tech will maintain records as necessary to comply with USDA, FDA, DEA, GLP and Comparative Medicine regulations and policies as well as AAALAC Int. standards for accreditation.
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fda job in Long Beach, CA
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