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In-depth experience of QC analytical methods and regulatory/pharmacopeia requirements for biologic or cell/gene therapy product testing and method validation for US, EMA and ICH regulations and guidance documents.
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Electrical, Software, Systems, Experience Design, Design Transfer, Quality, Regulatory. Create and modify PCBA design packages and electrical component specifications, including but not limited to electrical circuit schematics, PCBA manufacturing specification packages, and wire harness / cable assembly specifications for products currently in production phase.
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Your expertise in trust administration, fiduciary responsibilities, and client relationship management will ensure the effective execution of trust services while maintaining compliance with legal and regulatory requirements.
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Professional certification is highly desired - Certified Internal Auditor (CIA), Certified Information Systems Auditor (CISA), Certified Financial Services Auditor (CFSA), Certified Regulatory Compliance Manager (CRCM), Certified Public Accountant (CPA), Certified Fraud Examiner (CFE) or Certified Risk Professional (CRP.
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Extensive management experience in a cGMP testing laboratory environment, with knowledge of regulatory and compendial guidelines as related to cell-based assay requirements, aseptic processing, and biosafety of cell therapy products.
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The code Enforcement Officer is expected to perform a wide variety of code enforcement and professional administrative tasks, including inspections, evaluations, compliance processes, and enforcement of land use, zoning, business license, occupancy, nuisance, standard housing, and related provisions of the Municipal Code and other regulatory codes.
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This investigation includes but is not limited to a criminal, civil litigations and regulatory review, employment, education, and credit review (role dependent). We assist companies and non-profit organizations in delivering benefits to their employees.
$60,000 - $100,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Coordinate with other privacy, compliance, and risk management leaders in the company to ensure our programs are aligned, as well as staying connected to governance owners, including Privacy Regulatory Affairs and Corporate External Legal Affairs Front Line.
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Just-Evotec Biologics is seeking a Director/Sr. Director of Regulatory CMC to join a fast-paced, collaborative and multi-disciplinary team to lead all aspects of regulatory affairs for the advancement of low-cost biotherapeutics manufacturing.
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Administer, enhance and execute an effective compliance program designed to ensure regulatory requirements are met including for KYC/KYB, Anti-Money Laundering, sanctions, consumer compliance, and state money transmission regulations and guidance.
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Primary responsibilities will be to provide support to a team of regulatory experts, scientists, and engineers to prepare hydropower licensing, permitting and compliance documents, perform consultation with agency and stakeholder groups, and support project management activities in accordance with Federal Energy Regulatory Commission (FERC) requirements.
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The Retirement Benefits Technician provides administrative support associated with participant and Fund data in accordance with Company policies, regulatory requirements, and Plan guidelines. Zenith American Solutions is the largest independent Third Party Administrator in the United States and currently operates over 40 offices nationwide.
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Full understanding of GCP, GLP and GMP regulations and regulatory compliance guidelines. Perform audits on clinical investigator sites, vendors, processes, systems, and study documents to assure quality assurance compliance with regard to internal procedures as well as regulatory guidelines.
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Reporting directly to the Head of Communications of Gaming at Microsoft, the Xbox Communications Senior Director will serve as a trusted advisor to the Xbox communications and marketing teams as well as the Gaming Leadership, Social Media, Public Affairs, Investor Relations and engineering teams to drive storytelling around the gaming business that will shape the future of play.
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The Vendor Strategy Category Director will serve as the single point of business accountability in Clinical Development and Operations to support strategic sourcing, vendor selection, assessment, onboarding, and monitor performance of vendors in Oncology Regulatory and Medical Affairs Strategy.
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regulatory affairs jobs Title: regulatory affairs specialist Company: Amgen in Redmond, WA
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