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Maintain required documentation according to DDS, DMH, MassHealth, HUD, DPH, CARF, and all applicable regulatory standards as well as Bridgewell policies and procedures. Provide services to individuals according to DDS, DMH, MassHealth, HUD, DPH, CARF, and all applicable regulatory standards, as well as Bridgewell policies and procedures.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Obtain signed orders, reports and approval of treatment plans from primary physicians and specialists; and ensure that records/documentation meets regulatory requirements for MAP, DDS, DPH, CARF, MASS Health and Day Habilitation programming.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The LPN will assist with covering day habilitation hours as needed, residential Direct Care LPN hours as needed, conduct medication audits, and provide training and support to program staff. Reinforce a team approach, set clear expectations, provide feedback, communication and support to staff and individuals.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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This role reports directly to the Vice President of Human Resources for the Endoscopy division and will support R&D, Medical Affairs, Clinical, Regulatory Affairs, and Finance functions.
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Support regulatory compliance and the development, maintenance and improvement of documentation and processes. Key responsibilities/essential functions include: Support continuous improvement activities, including such areas as regulatory procedure development and documentation, aligning and standardizing approach across products and team.
$42 an hourExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Skills: estate planning,financial analysis,regulatory compliance,tax,accounting. Support the development of tax strategies to minimize tax liabilities for trusts and estates. The Senior Tax Accountant (Trust and Estates) plays a critical role in providing tax and accounting services for trusts and estates.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Responsible for leading and managing the analytical development and support of the analytical quality control strategies during late-stage and post-approval (commercialization) phases. The ASL Associate Director will also be responsible for implementing strategic initiatives that will develop and integrate best practices across brands, Analytical Sciences, and GPS. These initiatives will include, leading, and strategizing control strategy improvements providing robust Health Authority Strategies with a high probability of technical and regulatory success across the portfolio of biological brands.
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8-10+ years experience in the Biopharm/Pharmaceutical industry with cross-functional experience in one or more areas (i.e., research, analytical, quality, engineering, manufacturing, regulatory CMC, or IT.
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This role in Regulatory Affairs will be responsible for developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers.
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The Principal Consultant - Utility Regulatory Accountant is responsible for analyzing and compiling financial data through multiple sources to support regulatory filings for investor-owned utility companies across mostly North America.
$151,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Quality and Regulatory Support Manager for Cytiva is responsible for supporting the Business and Customers in a global environment by providing quality documents and regulatory support in ongoing projects, new product development, change control, and in response to customers' requests for quality, regulatory and technical-related information as it pertains to Bioprocess filtration products.
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This investigation includes but is not limited to a criminal, civil litigations and regulatory review, employment, education, and credit review (role dependent). We will support you while you learn the FINRA licensing material and work to obtain the Series 7 and 63 licenses.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Job Description: QA Lead Technical Operations, ProjectsOnsite, Devens locationWork Schedule: Mon - Fri, First shift (:AM - PM) Job Description/ Responsibilities:- Provides Quality Assurance (QA) support to Devens Site and reporting Manger through quality review andapproval of Investigations and Corrective Actions.
ExpandApply NowActive JobUpdated 5 months ago - UpvoteDownvoteShare Job
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The Environmental, Heath, and Safety (EHS) Coordinator is responsible for providing full time environmental health and safety support to manufacturing operations in compliance with applicable policy and regulatory requirements.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Provide support for the Quality Assurance and Regulatory Affairs processes that the team adheres to. The role will support with the management of Client’ s calibration and metrology program.
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regulatory support jobs in Bolton, MA
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