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As part of the Regulatory Affairs CMC team, you will report to the Executive Director and Head, CMC Regulatory Affairs Pharmaceuticals. Join Takeda as a Senior Director, GRA Pharmaceuticals- Small Molecule where you will establish collaboration with Global CMC teams and leadership through networks and enable CMC regulatory teams success in meeting goals/objectives.
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We are looking for a Manager of Food, Safety, Quality and Regulatory Affairs (aka FSQRA) to join our team remotely! High level experience of in food safety and quality regulations and standards (GMP, GFSI [SQF, BRC, other benchmarked scheme], HACCP, SSOP), government regulatory requirements, food safety, food manufacturing processes, technologies or other relevant area of responsibility.
$100,000 - $147,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The Director will advise and work closely with colleagues in creative, production, finance, marketing, publicity, consumer products, as well as with Business and Legal Affairs in other departments.
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Regularly interfaces with team members in R&D including Biostatistics and SAS Programming staff, Data Management, clinical research and operations teams, regulatory affairs, clinical pharmacology, medical writing, medical affairs and quality management.
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This position provides an opportunity to join the US Global Regulatory Policy & Advisory team as a subject matter expert, with a focus on providing policy guidance on the Fundamental Review of the Trading Book (‘FRTB’) / new Market Risk capital requirements within the US Agencies’ proposed adoption of the ‘Basel III Endgame.
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The Regional Medical Scientific Director (Medical Science Liaison) is a credentialed (i.e., PhD, PharmD, DNP, MD) Director Level Medical Affairs position and therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs.
RemoteExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Professional education and experience in any or a combination of the following disciplines can provide the base knowledge required to perform the work: Foreign Affairs; International Relations; History; Anthropology; Sociology; and related social science disciplines.
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Key Responsibilities The Medical Science Liaison (MSL) is a member of a field-based team of scientists who function as an extension of the US Medical Affairs organization. MSLs provide medical information through scientific exchange in a fair-balanced manner and provide clinical/scientific support for Bristol Myers Squibb and the Medical Affairs department at the direction of Medical Affairs management.
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Leading new business architecture required to support the Regulatory Capital computation per the Federal Reserve Bank Basel III requirements across the IHC. Extensive experience with Federal Reserve Bank Basel III regulatory Capital requirements, preferably at a Large FBO.
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This position reports to the Director, Global Strategy, Regulatory & Public Affairs. The TeamAmongst its other responsibilities, the Global Strategy, Regulatory and Public Affairs team leads on the development and implementation of Gates Ag One's regulatory science programs and related activities, such as regulatory studies, permit acquisition, and ensuring compliance with phytosanitary and biosafety regulatory requirements.
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The analyst will regularly work with senior members of Customer Operations, Regulatory and External Affairs, Transmission Operations, Finance, Accounting and outside consultants in performing these daily responsibilities and supporting strategic initiatives.
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Exercise product risk management related to ADTS activities (, technical recommendations), Product Stewardship and Regulatory affairs. The ADTS Engineer, MBS (Masterbatch Solutions) reports to the ADTS Director, USCAN. The primary focus of the ADTS Engineer - MBS will be on internal and customer interaction but is not limited to senior-level competence surrounding all aspects of primary and secondary [downstream] plastic and ancillary processing, tooling, part design, and material selection capabilities.
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Consistent adherence to field and corporate policies and Global Medical Scientific Affairs (GMSA) strategy, including field standard operating procedures (SOPs), Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities.
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Any other tasks requested by Team Lead, Head of Regulatory Compliance, Chief Compliance Officer and Chief Legal and Compliance Officer. Working closely with the Head of Regulatory Compliance, Chief Compliance Officer, Chief Legal and Compliance Officer and Asia Compliance team, this individual will work to strengthen the Company’s overall RCMP, while ensuring the timely identification, resolution and documentation of update of regulatory and compliance issues.
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Contacts are with a diverse multi-national audience including all 13 Invivo/Invitro Business Lines, Business Areas, External Customers, Regional Support Center, Customer Care Center, Education Services, CSML, Finance, Services Marketing, Customer Administration, Business Process Engineering (Quality) and Regulatory Affairs.
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regulatory affairs jobs Title: sr director Company: Biogen
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