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Provide oversight and implementation of procurement governance, policy design, continuous improvement programs, including regulatory compliance and policy compliance management. Understanding of best practices in Procurement, Compliance and Regulatory concepts.
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If an export authorization from an applicable US regulatory agency is required in connection with your employment, your employment is contingent upon Supernal’s receipt of such regulatory authorization(s) and your continued compliance with all conditions and limitations pursuant to such authorization(s.
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Technical knowledge of manufacturing systems, methods and procedures, biopharmaceutical manufacturing processes, knowledge of regulatory aspects (cGMP). Skills: Subject matter expert relative to manufacturing and MES Master Batch Records.
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Job Details Description This position develops, monitors, and maintains HUD and Tax Credit and other regulatory occupancy compliance at the affordable housing communities under the supervision of the Senior Compliance Specialist and Director of Compliance.
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Serves as an expert resource to other departments Manufacturing/Operations, Quality, Marketing, Regulatory Affairs, Clinical Studies, and International Technical Services), provides timely response and follow-ups.
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Management of lab equipment including, Qualifications, e.g. IQ/OQ, calibration and maintenanceParticipate in all GMP and operational training programs & complete associated Training RecordsParticipate in internal and external audits (including regulatory)Weekend work may be required as needed to meet production timeline schedules.
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Pharmacy Technicians take important steps to ensure all medication needs and regulatory compliance standards are met for our patients and they demonstrate ethical conduct and maintain patient confidentiality at all times.
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Develop and submit all applicable EHS permits, Forms, and reports to EPA, Wastewater, Fire Department, and other regulatory agencies. Strong track record of submitting permits, working with regulatory agencies, leading and developing EHS programs, performing audits, JHA, and gap assessment.
$98,200 - $157,200 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Review, create and coordinate document changes · Responsible for creating and updating inspection templates · Assist Customers with regulatory documentation like REACH, RoHS statements · Create and distribute final inspection reports per Customer requirements · Create internal quality documents related to QMS, quality alerts, PVPs etc · Assist on peer trainings for example on new procedures, procedure changes, new work instructions etc.
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Maintains adherence to regulatory requirements (e.g., USDA, FDA) and ethical standards in procurement processes. Maintains adherence to regulatory requirements (e.g., USDA, FDA) and ethical standards in procurement processes.
$49,000 - $54,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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In partnership with the team in New Mexico, implement the Performance Assurance Program to meet DOE/NNSA and other regulatory requirements. If you have a Medical Portable Electronic Device (MedPED), such as a pacemaker, defibrillator, drug-releasing pump, hearing aids, or diagnostic equipment and other equipment for measuring, monitoring, and recording body functions such as heartbeat and brain waves, if employed by Sandia National Laboratories you may be required to comply with NNSA security requirements for MedPEDs.
$97,500 - $187,500 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Analyze organizational readiness to implement strategy and work with sales, manufacturing, quality, regulatory, operations, and logistics partners to ensure an extraordinary customer experience.
$143,000 - $195,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Knowledge of regulatory compliance wireless and EMC processes. MiCOM Labs is a renowned international regulatory compliance laboratory specializing in testing and certification for wireless and telecommunication products.
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Biotechnology company is hiring a Regulatory Affairs Specialist III to manage activities associated with regulatory approval of in vitro diagnostic medical devices. 5 years of experience in regulatory affairs in In Vitro Diagnostics or medical devices.
$56.73 - $75 an hourExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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As a Manager in Supplier Quality Assurance, you will be responsible for leading a team of quality professionals in ensuring that suppliers meet the necessary quality standards and regulatory requirements.
$100,200 - $125,200 a yearFull-timeExpandApply NowActive JobUpdated Today
regulatory affairs jobs Title: regulatory affairs Company: Beigene in Pleasanton, CA
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