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Perform and document preventive maintenance and quality control procedures. Report accurate and timely test results to deliver quality patient care. [declination form required]Blood bank experience requiredASCP or AMT certification[preferred not required Description: Job Duties/Responsibilities:Responsibilities are interchangeable within job titles of medical laboratory scientist (MLS), medical technologist or clinical laboratory scientist.
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What we are looking for:A PhD in medical physics, imaging physics, physics of nuclear magnetic resonance, or related fields, ideally with an experimental component such as optimizing experimental design via metric development or quality control reporting.
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MelroseWakefield Hospital and Lawrence Memorial Hospital are distinguished by the range of high-quality clinical care and services. Participates in unit specific quality improvement projects i.e. hand washing audits, time-outs, refrigerator/medication logs, daily/monthly code cart checks.
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Reporting to the SVP CHCs, the Senior Medical Director, Community Health Centers (SMD CHCs) has primary responsibility for leading and directing clinical practice across Harbor Health’s Community Health Centers to ensure the delivery of high-quality and safe patient care, interdisciplinary collaboration, patient satisfaction, and provider satisfaction and engagement.
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Manager, Quality Systems Engineering - Medical Products page is loaded. Manager, Quality Systems Engineering - Medical Products. Manage the Medical Products Quality Team with a focus on ensuring operational excellence regarding improvements and strategy.
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Will provide essential medical and scientific expertise, review, advisement, and oversight to support development of high quality promotional and medical materials, internal training materials, and communications as part of the Promotional Review Committee (PRC) and Medical Review Committee (MRC.
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Collaborates with cross-functional team members, eg, Clinical Pharmacology, Toxicology, Research, Clinical Development, Regulatory Affairs, Biostats, Data Management, Quality, CMC, QC, etc., to ensure accurate and timely completion and delivery of high-quality, scientifically-sound documents, slide decks, and publications.
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The Sr. Advanced Manufacturing Engineer will act as a liaison between R&D, Supplier Development, Quality, and Operations team members assigned to the project. Proactively identify and evaluate potential contract manufacturing partners by analyzing quality, cost, delivery timelines, and regulatory compliance capabilities to recommend optimal providers.
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To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the Group research, develops and markets innovative drugs in its three therapeutic areas: AIR (products and services that promote respiration, from new-born to adult populations), RARE (treatment for patients with rare and ultra-rare diseases) and CAR E (products and services that support special care and consumer-facing self-care.
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Collaborate with executive leadership, clinical teams, and external stakeholders to develop and implement value-based care strategies that improve patient outcomes, reduce costs, and enhance the overall quality of care.
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The incumbent provides input into medical affairs activities, inclusive of high quality scientific and strategic communications and scientific congress coverage. Create strategic territory plans and metrics that align MSL activities with medical affairs objectives.
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Ophthalmic Consultants of Boston (OCB) was established in 1969 to offer patients the highest quality eye care and laser/surgical treatment. A Little About The Position:Gathers important patient medical history & accurately updates electronic medical record.
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Our numerous awards include being named a Top Performer on Key Quality Measures by The Joint Commission, receiving a national hospital safety score "A" rating by The Leapfrog Group, being recognized as a Top Hospital by US News & World Report, and earning a place on the Harvard Pilgrim Hospital and Physician Group Honor Rolls.
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EGenesis is seeking a Medical Writer to develop high-quality, technically accurate documents to support regulatory filings for our xenotransplantation programs. Develop and write high-quality, scientifically accurate documents for regulatory filings, including preclinical and clinical study reports, protocols, investigator brochures, and regulatory submission documents.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Thorough knowledge of the current quality and regulatory requirements for medical devices. Ensure that manufacturing has accurate and detailed information on specifications, with customer manufacturer under corresponding QMS (Quality Management System.
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quality job Title: medical Company: Inc in Melrose, MA
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