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Offers general guidance for Resource Conservation Recovery Act (RCRA), Department of Transportation (DOT), Toxic Substance Control Act (TSCA) and other applicable local, state, and federal regulatory bodies.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Ensure all scientific communications adhere to regulatory guidelines and industry standards including ICMJE guidelines. Familiarity with regulatory and publication guidelines regarding medical communications strategy and execution.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Current knowledge of State and Federal regulations, Joint Commission standards, HIPAA regulations, and Medicare COP to ensure compliance with all regulatory bodies. Provides administrative leadership to the Department of Case Management with responsibility for Utilization Review, Integrated Clinical Service, Discharge Planning and Care Transitions in accordance with Federal/State legal and regulatory requirements, as well as private payer guidelines.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Experience Minimum of 2 years' experience in instrument calibration and repair for manufacturing, laboratories, utilities, or facilities equipment in a pharmaceutical manufacturing, or high regulatory environment is accepted with degree, and in lieu of degree 3 years of experience will be accepted.
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In depth knowledge of acute care Case Management to include medical necessity, utilization review, LOS management, readmission reduction, denials management and effective transitions of care impacting revenue cycle.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Interpret study results and collaborate with HCPs (e.g., study Investigators, physicians) in the development of scientific communications content, such as conference proceedings (e.g., abstracts and presentations) and/or journal manuscripts.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Follow rules and regulations established by the NRC, state regulatory agencies, and JCAHO. Shields Health has an exciting opportunity for an PET/CT Technologist, to work Part-Time with flexible options.
Part-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Hello I'm Komal from Intellectt we have an opening for a Regulatory Affairs Specialist III in Mansfield, MA. Role: Regulatory Affairs Specialist III. Serves as the Regulatory Affairs lead on cross-functional MDR project teams.
Full-timeExpandApply NowActive JobUpdated 4 months ago - UpvoteDownvoteShare Job
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HOSPITAL WIDE RESPONSIBILITIES:Works within legal, regulatory, accreditation and ethical practice standards relevant to the position and as established by BWH/Partners; follows safe practices required for the position; complies with appropriate BWH and Partners policies and procedures; fulfills any training required by BWH and/or Partners, as appropriate; brings potential matters of non-compliance to the attention of the supervisor or other appropriate hospital staff.
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Act in compliance with Heritage Healthcare’s regulatory and professional standards and guidelines. The Certified Occupational Therapy Assistant (COTA) is a skilled technical worker who performs direct resident care activities under the clinical supervision of the Occupational Therapist.
$38 an hourPart-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Work with cross-functional partners, including but not limited to R&D, Clinical Affairs, Regulatory Affairs, Health Economics & Market Access (HEMA) and Marketing to provide leadership with product development and commercial plans to support product launch, training content and delivery.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Schneider Electric is seeking a Senior Legal Contract Manager (Government) in its Legal Department with experience in government and commercial contracting, grant awards and related Legal and Regulatory compliance.
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Transamerica is organized by lines of business (Life Insurance, Annuities, Mutual Funds, Retirement Plans, and Employee Benefits), which are supported by Transamerica Corporate (Corporate Development; Finance; Internal Audit; Legislative, Regulatory & Policy; Office of the CEO; People and Places; Brand; Corporate Affairs; Risk; and Technology.
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Knowledge of FDA, ISO, and EU MDR regulatory requirements as applicable to medical devise preferred. Part of a team of technical subject matter experts (SME) for all chemical and toxicological aspects of Chemical Characterization testing related to medical devices including current accepted practices, global regulatory requirements, current and developing scientific principles and concepts, and study design, execution, interpretation, and reporting.
$126,800 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Candidates familiar with GLP, GMP, GCP, CLIA, and ISO regulatory guidelines. Ensure that work product complies with Precision’s SOPs, regulatory requirements and customer expectations. Candidates familiar with GLP, GMP, GCP, CLIA, and ISO regulatory guidelines.
$100,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago
regulatory job in Mansfield, MA
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