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Assists the Assistant Dean of Student Affairs in determining resource allocation, including budgets and staffing, for student programs, organizations, and events. Essential Duties and Responsibilities: Under the direction of the Assistant Dean for Student Affairs, do the following: A. Guide to Professional Success (GPS) –Scheduling - Oversees and manages GPS CalendarSchedules rooms and appropriate educational technology support for GPS sessions Communication - Manages GPS communication Ensures timely and effective correspondence with session presenters, learning community mentors, and students via email, news board, and student assignments.
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QualificationsTo be considered for this role, you’ll require a minimum of 5 years of professional experience in relevant field of healthcare products or related activities e.g.:Work in medical devices industry and/or in vitro diagnostic devices(preferred) or closely related industries (e.g., pharmaceutical industry) such as research and development, manufacturing, quality management, regulatory affairs.
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The FHCC is a first-of-its-kind partnership between the US Department of Veterans Affairs and the Department of Defense (DoD), integrating all medical care into a federal health care facility with a single combined VA and Navy mission: "Readying Warriors and Caring for Heroes.
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Engage with regulatory agencies and industry stakeholders regarding regulatory and legislative affairs, including by providing feedback on proposed regulations. 2-5 years' experience working in regulatory compliance or regulatory affairs for a consumer products, food, beverage, cosmetics, or pharmaceutical company, or in a highly regulated industry.
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The position of Regulatory Affairs Specialist II is within our Infectious Disease business unit. Title: Regulatory Affairs Specialist II - 5 Openings. 4 years' experience in Regulatory Affairs role.
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You will report to the Director, Corporate Affairs Operations and will support teams within Corporate Affairs that includes Legal, Ethics and Compliance, Security Loss & Prevention and Environmental Health & Safety.
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The primary purpose of this position is to provide financial education, counseling, and information & referral services to assist clients with personal financial readiness, money management, debt liquidation, and consumer affairs.
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6+ years of progressive medical/scientific affairs experience within the pharmaceutical, biotech industry or at a consulting firm that supports the pharmaceutical or biotech industry; at least 3 years driving medical strategy.
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This includes the management and preparation of various critical regulatory documents such as: product Safety Data Sheets, product labels, product attestation documents and certifications.
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Strategic support to the IMCO/IMAP commercial (Immunology, Oncology and Specialty VPs and GMs), Medical Affairs and functional leadership on a variety of legal matters impacting key priorities. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.
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Experience working with CPG technical roles in Research and Development, Quality, Manufacturing, Procurement or Government Affairs related to Medical Device, OTCs and/or Supplements. Bachelor’s degree and at least 4 years of experience in Regulatory Affairs and/or Compliance OR a High School diploma/GED and at least 7 years of experience in Regulatory Affairs and/or Compliance.
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This position is in-person and on-site at the Snap-on Diagnostics Facility in Lincolnshire, IL. The Marketing intern will help support the Marketing team with binder preparation and events, make outgoing phone calls, documentation preparation, website maintenance, social media, community event support, proofreading, data entry, and general office administration.
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Drive continuous improvement and evolution of the Congress channel by working with Strategic Brand Marketing teams, Medical Affairs and Commercial divisions to gather insights and customer feedback on Congress experience, ensuring learnings and improvements are embedded into future events and/or processes.
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Minimum 7+ years of progressive experience in medical devices/IVD/biotech industry Regulatory Affairs required, including experience in Armed Forces. The Senior Manager position in Regulatory Affairs leads the regulatory strategy for new and modified Sysmex medical device products.
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Hybrid Senior Manager, Regulatory Affairs - Lincolnshire, Illinois. Minimum 7+ years of progressive experience in the medical devices/IVD/biotech industry Regulatory Affairs, including experience with regulatory agencies.
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affairs job Title: intern Company: Amgen in Mettawa, IL
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