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The role of the Manufacturing Technician/Scientist is to contribute to the high-quality and regulatory compliant manufacture of a variety of DNA based IVD kits and components to demanding quality specifications, and to ensure that the laboratory environment is operating effectively and safely in accordance with instruction provided by the Manufacturing and QC Manager.
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Job Overview:The Junior to Mid-level Global Franchise and Supply Network Associate Attorney will work on a variety of matters related to franchise and distribution law, including structuring and developing franchise programs, drafting legal documents, advising clients on compliance and regulatory matters, and resolving franchise-related disputes.
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Technical Excellence: Provide expert advice on fire safety design, strategy, and compliance, ensuring that all work meets regulatory standards and best practices. As an Associate Chartered Fire Engineer, you will play a key role in leading fire engineering commissions, interfacing directly with clients, and helping to develop and expand the fire engineering service offering in London.
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Our client is currently hiring for a Customer Service Associate (Greek speaking) to work on a hybrid basis at Chester, UK. Title: Customer Service Associate (Greek speaking) We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
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If current Policy, Procedure and/or Protocols are not in alignment with state regulatory guidelines, the Nurse Consultant is to immediately notify the Director and/or VP of Clinical Service and work jointly to update practices for that state to ensure regulatory compliance.
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Director, Model Validation for SHUSA Compliance models (Transaction Monitoring, Sanctions Screening, Fraud Risk, etc) will be responsible for leading the independent validation of models used by various Compliance groups in conformance with regulatory guidance on model risk SR- and other regulatory requirements around Compliance models.
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As a Preclinical Study Director, you will oversee the planning, execution, and reporting of preclinical studies in compliance with regulatory standards (e.g., GLP). Ensure all studies are conducted in compliance with Good Laboratory Practice (GLP) regulations and other relevant regulatory guidelines.
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Responsible for developing strategies and overseeing the execution of technical activities associated with product development and manufacturing, supporting clinical development, regulatory filings (IND/NDA/MAA), and product approvals and commercialization.
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Oversee and monitor effective compliance programs aligned with current industry best practices, regulatory guidance, and compliance practices, but not limited to fraud risk management, monitoring suspicious transactions, the Customer Identification Program (“CIP”), due diligence compliance and drafting/updating policies and procedures related to BSA/AML/OFAC compliance.
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Liaison with the NOC Manager and NOC Associate Security Officer to ensure that all operating processes meet the regulatory compliance of all governing US Agencies and satisfies all contractual obligations.
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Position Purpose: As part of Sunshine Health Plan's Payment Integrity Compliance team, the Compliance Analyst will assist in maintaining Centene Corporation's Compliance Program; guide special projects; provide regulatory interpretation; perform compliance reporting; and develop and implement compliance auditing and monitoring strategies.
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The Director of Trade and Customs Compliance will oversee and manage NLA's global trade compliance program. 10+ years relevant import/export customs compliance/regulatory work experience.
$175,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Report to the Director, Assistant General Counsel, Regulatory and Transactions, and work cross functionally with the Company’s Trade Compliance, Security, Employee Relations, and Communications functions to provide oversight and development of programmatic compliance programs and procedures to ensure adherence to relevant laws, regulations, and industry standards.
$204,000 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Responsibilities: Oversee and direct all CMC regulatory strategies in compliance with global regulatory requirements for the development of ORIC’s products. Excellent CMC technical writing and communications skills with a strong background in small molecules, ideally solid-oral dose formulations, manufacturing, and regulatory writing.
$235,000 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Job Title:Assistant/Associate Director - Histocompatibility LaboratoryDepartment:University Hospital | Tissue TypingScope of Position Individual is responsible for histocompatibility laboratory compliance with regulatory and accreditation agency standards, quality assurance, development of laboratory processes & clinical protocols and budget preparation & monitoring.
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