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Engages routinely with leadership from cross-functional partner teams such as Global Product Strategy, Compliance, Regulatory, Program Management, Clinical Development and any other BioMarin stakeholders associated with U.S. Commercial activities to evaluate strategic considerations across the portfolio of products.
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Reporting to the VOXZOGO Global Commercial Lead, the VOXZOGO Marketing Director, will lead key strategic initiatives to support the global growth and ongoing commercialization of VOXZOGO. S/he will lead value creating workstreams, working across regions and developing strong partnerships with our key strategic markets, market access, medical affairs, technical operations and supply chain, regulatory and worldwide Research and Development.
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The Oligonucleotide Production Technician I will perform tasks associated with the production of modified oligonucleotides in a high throughput time sensitive manufacturing environment in compliance with company procedures and external regulatory requirements.
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The Director, US Achondroplasia HCP Marketing Lead is responsible for overarching HCP vision, strategy and tactics for the cross-functional brand team for Voxzogo in achondroplasia and lifecycle opportunities in the US. They must be a seasoned leader who can influence without direct reporting relationships across all key stakeholder teams in the US (sales, reimbursement hub, market access, global product strategy, medical affairs, compliance, learning and development, etc.
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Develop collaborative relationships with various groups internally and externally, including clinical and support staff, other departments, management, Sutter Health clinical nurse educators, college staff, regional CPR training program coordinators, and regulatory agencies to coordinate educational needs and ensure compliance.
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Must be professionally licensed by the State of California, Board of Behavioral Sciences as a Licensed Clinical Social Worker, Licensed Marriage and Family Therapist, or a Licensed Professional Clinical Counselor OR must be professionally licensed as a Clinical Psychologist issued by the State of California Department of Consumer Affairs, Board of Psychology.
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Our consultant pharmacist teams lead the industry in clinical excellence, meeting the challenges of higher acuity, greater regulatory scrutiny, and staffing constraints head-on. This enables facilities to enhance care delivery, minimize regulatory risks, and adapt to rapid changes.
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Helping clients with everyday transactions such as deposits, withdrawals, payments, reordering a debit card, setting up a direct deposit or helping update their address, accurately and efficiently, while complying with all policies, procedures and regulatory and banking requirements.
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They must be a seasoned leader who can influence without direct reporting relationships across all key stakeholder teams in the US (sales, field based clinical support, reimbursement hub, market access, trade and distribution, global brand management, medical affairs, compliance, learning and development, etc.
$334,400 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Participate in safety orientations, weekly meetings, toolbox talks, pre-installation meetings, RFI and submittal process, storm water management, inspections, and other regulatory requirements.
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Manage the GAAP classification process Perform ERP administrative tasks (e.g., maintain manager posting limits, delete unposted journal entries, monitor and delete records in the GL interface table, fix corrupted Balances, add a missing FX rate, rereview COA audit report, COA local to GAAP mapping, CMAAR Med Affairs Allocation, etc.
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The Per Diem Nurse is responsible for meeting all regulatory documentation standards. The Per Diem Nurse participates in the multidisciplinary team, Quality Assurance, and Utilization Review activities.
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Ensures any additional pricing tasks related to local regulations and/or regulatory compliance programs are completed accurately and within the required time frame. Assists manager or assistant store manager in reviewing order exceptions on order release day and assists in reverse logistics (e.g., 1506, returns, empty package.
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These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.
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Ensure manufacturing adherence to company policies/procedures, regulatory licenses, industry standards, and GMP regulations. Working knowledge of United States and European regulatory requirements, guidelines, and recommendations a plus (additional jurisdictions a plus.
$38 an hourFull-timeExpandApply NowActive JobUpdated 11 days ago
regulatory affairs jobs Title: regulatory Company: Jobget in Novato, CA
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