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Provide services to individuals according to DDS, DMH, MassHealth, HUD, DPH, CARF, and all applicable regulatory standards as well as Bridgewell policies and procedures. Summary: The Developmental Specialist 3 will provide support and assistance in Level 3 day habilitation programs.
Full-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Our successful candidate will have experience preparing state and Federal environmental permit applications, interacting with regulatory agency representatives, conducting natural resource assessments, performing waters/wetland delineations in New England, familiarity with the 1987 USACE Wetland Delineation Manual and Northcentral and Northeast Regional Supplements.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Assisting in regulatory compliance with applicable federal environmental laws (National Environmental Policy Act (NEPA), Endangered Species Act (ESA), National Historic Preservation Act (NHPA), Executive Orders (E.O.) 11988, 11990, and 12898; other laws, regulations, and E.O.s.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Work closely with Regulatory, Clinical Affairs, Quality Assurance personnel to align with Post Market Surveillance activities. Stay appraised of latest developments in the regulatory landscape related to Post Market Surveillance.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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More specifically, you will plan, organize, and/or direct cyber, IT, COMSEC, and information/knowledge management (IM) activities which comply with legal, regulatory, and AF/DoD-directed requirements and meet mission and customer needs.
$151,870 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Acts as regulatory specialist on development project cross-functional team processes. Collaborates with other functional work teams e.g., Preclinical, Clinical, Medical Affairs, Manufacturing and Quality Control, providing regulatory guidance to aid in preparing, reviewing, and approving of regulatory NDA/IND/CTA/IMPD submissions materials.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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We are looking for a Sr. Regulatory Affairs (RA) Specialist who wants to grow your skills and take the lead on U.S. and international medical device submissions. Are you our next Sr. Regulatory Affairs (RA) Specialist.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Your Talent Acquisition Specialist can share more about the specific salary range for your preferred location during the hiring process. Able to facilitate technical review meetings and explain content to technical and non-technical audience members including but not limited to software, analytics, Site reliability engineers, Cloud Operations, Clinical, Medical, Marketing, Data engineering, Privacy, Regulatory, Product owners, Product Managers.
$152,955 a yearFull-timeRemoteExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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The Principal Regulatory Specialist is responsible for carrying out Pre-Market and Post-Market regulatory activities in compliance with Digital Factory’s Quality Management System for domestic and various international markets for SaMD products.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Experience: Minimum of 10 - years’ experience in regulatory approval processes for medical devices or in vitro diagnostics, with at least 5 years related to software as a medical device (SaMD.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Work with the Anika Regulatory team to create a comprehensive Master Control document control system. The Customer Care Specialist II is fully responsible for all Anika Inc customer orders, documentation, and other activities required to support commercial activities.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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We are looking for an Executive Director Specialist RN that will travel to many of our branch locations throughout our East Region as a hospice subject matter expert - minimum of 75% travel required You will serve as the administrator on call and are responsible for the overall operation at the local office, employment of qualified Hospice personnel, and provision of Hospice services.
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I'm Chandrasekhar, a Staffing Specialist at Intellectt Inc. as it is a regulatory implementation/remediation effort for China that will take the Gap analysis that has been done and look at the Gaps to determine what is missing and how to fix it.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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The Document Control & Records Specialist will support the Quality Team and will be responsible for daily support activities related to document control and archiving. Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, company policies, operating procedures and processes.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The QA Compliance Specialist I performs quarterly audits support internal audits and participates in customer and regulatory audits as part of the Audit Team. Job requires maintenance of up to date knowledge of all applicable international regulation and regulatory guidance.
Full-timeExpandApply NowActive JobUpdated 10 days ago
regulatory specialist jobs in Acton, MA
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