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The position of Scientific Affairs Director is within our Toxicology business unit. Data review for immunoassay screening and mass spectrometry results. The position of Scientific Affairs Director is within our Toxicology business unit.
$286,700 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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More details on our benefits can be found on our website at to the Chief Compliance Officer, the Assistant General Counsel - Regulatory Affairs provides legal support to each of ITW’s Segments and Corporate functions as needed on a variety of regulatory matters, with a principal focus on monitoring and advising ITW businesses regarding existing and developing legal and regulatory issues affecting the company’s operations and products.
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This role will provide CMC regulatory support and guidance for assigned projects and interfaces with R&D, Project Management, Manufacturing, Quality, and Regulatory colleagues to ensure a robust CMC regulatory strategy is developed and implemented to have on time submissions with the highest quality to meet global health authority expectations.
$225,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Regulatory Specialist will support the Legal and Regulatory Departments with monitoring and assessing the implications of existing and pending laws and regulations on RCP products and advocating for RCP's interests.
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The Associate Scientific Director provides medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions (HCP’s, Patients and Payers); generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, data, guidelines, and value proposition); safeguarding patient safety (risk minimization activities and safety surveillance activities.
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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. Required Knowledge: Regulatory, Scientific/Technical, QA, Business acumen.
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You will report to the VP, Communications and Public Affairs and be expected to work in either Lake Forest or our Chicago, IL office 3 times per week. You will report to the VP, Communications and Public Affairs and be expected to work in either Lake Forest or our Chicago, IL office 3 times per week.
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Title: Regulatory Affairs Associate Jr. Manager regulatory submissions ot ensure timely regulatory approval of medical devices. Ensure all client product and procedures comply with applicable regulatory agency requirements and guidelines.
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Role: Regulatory Affairs Associate Jr. Ensure all client products and procedures comply with applicable regulatory agency requirements and guidelines. Experience: 1+ years experience in a medical device or similarly regulated industrySkills: Ability to schedule and organize multiple projectsEducation: BS Engineering or ScientificDuties: Manager regulatory submissions to ensure timely regulatory approval of medical devices.
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Job DescriptionThe Director, Information Services reflects the mission, vision, and values of NM, adheres to the organization's Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards.
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The Government & Policy Affairs Group (GPAG) is Capital One's voice in the legislative and political processes. This role is also eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI.
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You will act as one of the primary spokespersons for the company with key opinion leaders, at global scientific conferences and advisory boards, and regulatory agencies and accountable to ensure that Worldwide Medical (WWM) global policies and standards are followed and supported for all aspects of Clinical Nutrition, IV Fluids and Pharmacy Solutions Medical Affairs and work is done with high ethical standards.
$286,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Interfaces with the regulatory affairs office at the producers and ensures our products meet the required government regulations. The Regulatory Specialist role is responsible for acquiring and providing the necessary document support for regulatory requests, requiring frequent interaction with internal and external personnel.
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The Project Manager provides project leadership for high-visibility, highly complex compliance initiatives across multiple business units and functions around the globe.
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The Project Manager provides project leadership for high-visibility, highly complex compliance initiatives across multiple business units and functions around the globe.
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Title: regulatory affairs Company: Inventiv Health Clinical in Deerfield, IL
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