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10+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs / small molecules.
$100 - $113 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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With minimal direction the incumbent manages the global regulatory CMC activities except Asia for all assigned Taiho Oncology Inc., (TOI) projects; provides strategic regulatory guidance especially for CMC during drug development, approval and post approval processes and commercialization, in coordination with internal staff, Japanese colleagues at Taiho Pharmaceutical Corporation (TPC) and external consultants/contractors.
$197,000 - $232,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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As the Regulatory Affairs Operations Specialist, Ad/Promo, you will play a pivotal role in ensuring regulatory compliance and operational efficiency within our organization.
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Recommend solutions for required changes to life support systems based on analyses of water quality data, system trends, animal observations, regulatory and water discharge requirements, and water flow needs, in collaboration with Applied Water Science, Husbandry, and other departments.
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Advanced knowledge of industry, regulatory or Department of Energy/National Nuclear Security Administration (DOE/NNSA) complex codes, standards, and criteria pertinent to the particular engineering discipline.
$170,430 - $262,668 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This area of responsibility is from the front wheel wells to the windshield and is where driver ergonomics, endless option content, and regulatory/compliance all converge to create a unique engineering and configuration management challenge.
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For the health and safety of our team members and residents, Oakmont Management Group may require team members to vaccinate, participate in daily screening, surveillance testing, and to wear face coverings and other personal protective equipment (PPE) to prevent the spread of the COVID-19 or other communicable diseases, per regulatory guidelines.
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Understanding of diverse regulatory standards such as PCI DSS requirements and SOX regulations. Evaluate and respond to submissions to the Peloton Coordinated Vulnerability Disclosure (CVD) program.
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Facilitates requests from national and/or local customers for information supporting compliance with Sysco, Regulatory, or Customer requirements such as questionnaires, surveys, COI, HHA, provision of BRC Food Safety Certificates, food safety audits for suppliers, and shelf-life data, etc.
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As Coach Cleaner, you'll: Perform cleaning assignments for train cars in accordance with FDA and Amtrak standards and guidelines; Drain and flush waste tanks; Vacuum, mop, dust, sweep, wash walls and windows; Use chemical cleaners, equipment and material in accordance with regulatory agencies and HAZCOM guidelines and procedures; Maintain proper care and use of materials, equipment, machines and hand tools.
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Establish and implement policies, procedures, and processes in response to DOE/NNSA/LLNS and other regulatory requirements, including taxing authorities. Supervise exempt staff, providing leadership and day-to-day work direction including review of written analysis, journal entries and interpretation of complex financial policies, guidance and regulatory requirements.
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We are seeking a Principal Regulatory Affairs Specialist to join Abbott's Heart Failure Division on-site in Pleasanton, CA. As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to provide support for the regulatory department, ensuring efficient and compliant business processes and environment.
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XperiencOps, Inc., is seeking an IT Operations Specialist with a focus on Helpdesk support to join our dynamic team. Proven experience as an IT Helpdesk Specialist, Systems Administrator, or similar role, with a strong background in managing IT operations and support.
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Basic knowledge of industry and regulatory standards, design criteria and codes relevant to Instrumentation and Controls. Intermediate knowledge with PLC programming: Rockwell RSLogix 5000 (required), Allen Bradley, Delta V, Siemens, Exposure to multiple PLC manufactures and platforms.
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Experience in Regulatory Reporting such as Basel III, Dodd-Frank, MiFID II. Solid understanding of data mapping, validation, and transformation processes for regulatory reporting purposes.
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regulatory affairs jobs Title: regulatory affairs specialist Company: Beigene in Pleasanton, CA
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