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This means that, in addition to our blockchain expertise, part of our operational needs are very similar to that of a traditional investment manager: trade management, service provider relations, book reconciliation, audit, tax, and regulatory compliance, and the like.
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US Regulatory Operations Lead, CHC page is loaded US Regulatory Operations Lead, CHC Apply locations Bridgewater, NJ time type Full time posted on Posted 3 Days Ago job requisition id R2720807 US Regulatory Compliance & Operations Lead, CHC Location: Bridgewater, NJ.
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SCOPE OF RESPONSIBILITY AND ADDITIONAL ROLES AND RESPONSIBILITIES: ·Third-party compliance service provider relationships and performance·Manage Compliance Risks Responsible for partnership with Kenvue Domestic and International Transportation teams, Kenvue Legal, and outside legal counsel for all Regulatory Compliance issues Manage third-party compliance service provider relationships by setting performance expectations and holding compliance service providers accountable for performance.
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Partner with Manufacturing, Product Support, Microbiology, Regulatory Affairs, Quality Control Labs, Engineering and Compliance. The Quality Engineer II will provide compliance and technical support to Manufacturing on all aspects of the biological manufacturing process controls at the Raritan manufacturing site for the Transfusion Medicine line of business.
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Key Activities/Responsibilities Manage all Government Pricing compliance obligations - policy updates as required to business or regulatory changes, Bona Fide & Non-Bona Fide Service Fee monitoring for treatment in calculations.
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Provide strategic direction on toxicology from discovery throughout market application for programs in different therapeutic areas, ensuring alignment with company objectives and in compliance with regulatory guidelines and industry standards.
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This position reports to VP, CDMA with a dotted line reporting relationship to the CSO. The Senior Director CDMA will interact with internal colleagues in Research and Development (Clinical Development & Medical Affairs, Strategic Operations, Evidence Generation & Data Sciences, Regulatory Affairs, Pharmacovigilance) Strategy/Portfolio Management,Commercial and Operations functions.
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The AD SAS, in partnership with the Medical Safety Officer (MSO), is responsible for the preparation of scientific safety analysis and evaluations, which are required for regulatory compliance and to aid in safety-related decisions for marketed products and products in development.
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Title: Data Architect in Regulatory with Databricks, Datafabric, Data mesh, Snowflake (Required) Client Innovative Medicines is seeking an experienced IT Solution Architect to support systems product development in Global Regulatory Affairs.
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Technical knowledge in metrology, calibrations, instrumentation, automation PLCs, VFDs and electrical practices generally attained through hands-on experience, cGMP compliance, EHS and regulatory standards (e.g. EPA, OSHA and DEA.
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Partner and manage relationships with contractors to ensure quality of work and compliance with all company policies and regulatory guidelines. EHS and regulatory standards (e.g. EPA, OSHA and DEA.
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This role will also play a key role in the Privacy, Forced Labor, and Product Regulatory programs and support a range of compliance activities, such as maintaining and communicating compliance policies, updating compliance education programs, process development, implementation, and monitoring.
$135,000 - $155,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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He/She maintains an up to date knowledge of ways of working and SOPs and develops a comprehensive understanding of global CMC regulations and guidelines to enhance probability of regulatory success and regulatory compliance.
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Pace Life Sciences provides a full suite of contract CMC development, CTM manufacturing, regulatory compliance, consulting, and facility support services to the pharmaceutical, biopharmaceutical, and gene therapy industries from our network of CDMO sites, GMP analytical testing laboratories, and manufacturing support service centers.
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At least 5 years of experience in a Solution Architect role serving the Regulatory Information Management domain. 7+ years of experience supporting pharmaceutical content management solutions and integration (Authoring, Submissions, Archival, TMF, Quality, DAM, PLM.
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regulatory compliance jobs Title: pharmacy technician Company: Cardinal Health in Neshanic Station, NJ
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