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Ensoma is seeking an experienced GMP Quality Assurance professional to use your resourceful and innovative thinking for a highly visible role within our rapidly growing company. Help to build the internal quality management system, including the development of vendor management and batch disposition processes.
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Responsible for Quality & Controls Assurance programs, activities and reviews, including claims reviews; call center and digital communications reviews; Medicare Risk Adjustment, HCC, clinical and coding reviews; DRG and medical records reviews; technology/systems and coding upgrade and implementation reviews (e.g. final user acceptance testing, etc.
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Prime Medicine is seeking a co-op for the Spring 2025 semester with experience in biological or chemical techniques to join the Analytical Development and QC team.
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Apply your topical knowledge and experience in one or more of the following: Quality, Risk Adjustment, Provider Data, Healthcare Data Interoperability, Value-based Care, Population Health, and/or Clinical Operations/Medical Cost Management to drive data solutions product innovation.
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Monitor the technical quality and accuracy of incoming and outgoing on-air programming from the master control room. Check studio equipment for proper functioning and notify Engineering of technical malfunctions affecting the quality of the broadcast.
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Job Description : POSITION OVERVIEW: The MassHealth Systems Teams unit seeks a highly motivated individual as a Data Warehouse Snowflake Migration Tester to join its Systems Quality Assurance (SQA) team.
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The Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up activities to ensure clinical trials are executed with high quality standards in compliance with regulatory requirements, GCP, and company SOPs. This role is based in our Waltham, MA headquarters.
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Clinical Trial Initiation Manager will deliver high quality and timely global study start-up. Coordinate contract and budget negotiations between sites and internal function team and coordinate investigational product release authorization with quality assurance.
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Responsible for external outreach with KOLs and key clinical trial sites to provide feedback on study feasibility and study start up activities. Oversee the informed consent process and translation of study required documents and participate in the development of study start up plans.
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Product Oversight : Ensure exceptional execution in delivering top-tier Software-as-a-Service (SaaS) solutions, maintaining a keen eye on product quality and user-centric design. With a focus on scientific computing and GPU acceleration, this role is pivotal in ensuring the efficient performance and scalability of our high-speed computing technology to deliver high-quality SaaS solutions.
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As a Joint Commission Certified Agency, our commitment to quality, integrity, and exceptional service has made us a trusted name in the healthcare staffing landscape. Cardiac Cath Lab Technologist 09/09/24 to 12/07/24 13 Weeks 40 Hours/week 10H Days 07:00 AM - 05:30 PM Boston, MA About TalentBurst, Inc TalentBurst Health & Life Sciences is an established provider of healthcare workforce solutions, servicing healthcare facilities across the United States for over 15 years.
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The Clinical Trial Manager, Site Start-up role plays a significant contribution to the clinical trial execution and ability to meet the corporate study goals for the Company clinical Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up activities to ensure clinical trials are executed with high quality standards in compliance with regulatory requirements, GCP, and company SOPs. This role is based in our Waltham, MA headquarters.
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As a Lab Production Technician, you will be responsible for: You will perform complex compounding, manufacturing (cyclotron and chemistry module operation) and quality control processes (utilizing analytical equipment TLC, HPLC, GC), under supervision as required by State and Federal law.
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The ideal candidate will have extensive construction management experience, plus at least some design experience, in land development, including a thorough working knowledge of contracts, safety, construction means & methods, scheduling, estimating, subcontractor management, and quality control.
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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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quality job Company: Inc in Melrose, MA
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