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... summarizing data and trends. Preparing regulatory filings Contribute to streamlining current ... candidate will have 2-5 years regulatory compliance experience working for an ... working for an exchange, a..
... summarizing data and trends. Preparing regulatory filings related to AML & ... candidate will have 5 years regulatory compliance experience working for an ... working for an exchange, a..
... trends. Conduce quality assurance on regulatory filings Contribute to streamlining current ... ideal candidate will have some regulatory compliance experience working for an ... working for an exchange, a..
Who We Are For more than two decades, going our own way has led to countless breakthroughs, bettering the lives of those suffering from rare genetic disease. In 1997 we were ..
... control to ensure we meet regulatory standards, and procure the needed ... and GMP core management, and regulatory compliance with worldwide requirements.u00A0 The ... as groups outside of TOPs..
Title: Research Associate 2- Chemical, Drug Product and Devices Technologies (CPDT)u00A0BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare ..
... control to ensure we meet regulatory standards, and procure the needed ... written technical reports, contributes to regulatory submission documentsu00A0Contributes to the overall ... have a broad knowledge of..
... control to ensure we meet regulatory standards, and procure the needed ... changes Interpret and apply applicable regulatory guidelines and directives (e.g., 21CFR, ... stakeholders appropriately Review and author..
Who We Are BioMarinu2019s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, ..
WHO WE ARE For more than two decades, going our own way has led to countless breakthroughs, bettering the lives of those suffering from rare genetic disease. In 1997 we were ..
Who We AreBioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, ..
... prior knowledge of ICH and regulatory submission is a plus.u00A0u00A0RESPONSIBILITIESu00A0Lead analytical ... strategy. Support pre- and post-IND regulatory submission by authoring and reviewing ... and responding to queries from..
BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and ..
... implementing federal, state, and local regulatory mandates Working as the liaison ... liaison to management to ensure regulatory compliance with applicable laws, regulations, ... implement federal, state, and local..