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2+ years of server level/Client testing experience as Quality Assurance Engineer, Software Engineer in Test, or SDET; Here you have the opportunity to cooperate with the world's top AI scientists, get in touch with the most cutting-edge technology, and provide quality assurance for artificial intelligence products serving hundreds of millions of people around the world.
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Thorough knowledge of quality assurance, quality improvement, utilization review, risk management, and accreditation and licensing requirements including The Joint Commission, NCQA, Knox-Keene Act, Federal HMO Act, CMS, Cal-OSHA, Public Employees Medical and Hospital Act, HIPAA and Medi-Cal regulations and standards.
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Leads quality assurance for both molecular genetics lab and cytogenetics lab. Oversees quality assurance and regulatory compliance across the laboratory. Coordinates quality assurance for the integration of laboratory information systems.
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Areas of work include Sensing Hardware Engineering, Sensing ASIC Architecture, Algorithm Engineering, Machine Learning Engineering, Deep Learning, Firmware Engineering, Software Engineering, Quality Assurance Engineering, and User Studies and Human Factors Engineering.
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Lead CAPA projects (or work closely with Quality Assurance) related to product quality or non-conformities and investigate customer complaints. The Senior QC Scientist is expected to use technical expertise to develop and document quality processes that support the R&D design & development and ensure the reliability and reproducibility of instruments and reagent products.
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Strong communication and organizational skills are required to oversee the transfer of new products into the Quality Control workflow, resolve problems, improve processes, and manage QC stocks.
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This position is responsible for ICD-10 Coding and OASIS Review, quality assurance, accuracy and overall integrity of the clinical records and documentation completed by Clinical staff. This position is responsible for ICD-10 Coding and OASIS Review, quality assurance, accuracy and overall integrity of the clinical records and documentation completed by Clinical staff.
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Responsibilities will vary depending on department of assignment (e.g., Emergency Room/Clinic, advisory to non-medical administrator, infection control, nurse/health education development, quality assurance, nurse anesthetist, etc.
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Prior experience in core assurance services conducting audit planning, developing audit programs, performing testing and preparing work papers is required. We are looking for a passionate Assurance Partner serving an evolving and exciting industry.
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Manage executive calendars: SVP Operations, EVP Technology and Clinical Development, and SVP, Regulatory Affairs, and Quality Assurance, including scheduling meetings and resolving schedule/resource conflicts.
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Minimum 6 years of experience in a biotech or pharma with relevant work experience within a quality control team. Review and track PLC projects to ensure quality tasks are completed on time.
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Work with product development teams to transfer design into manufacture with good quality assurance. Have knowledge and experience of quality control and assurance in a volume production.
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The Associate Director Quality Support, under the supervision of the Regional Executive Director, is responsible to manage quality assurance structures in large geographic regions consisting of multiple counties, programs and contracts representing substantial agency revenue.
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As a member of their Quality team, you will report to the Director of Product Assurance and will help define the inspection process for our first certified aircraft. Support the development and rollout of Advanced Product Quality Planning techniques such as PFMEAs, control plans, and SPC.
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The Senior Supplier Quality Engineer will be responsible for the quality oversight of Onto Innovation suppliers and contract manufacturers. Six Sigma Green/Black Belt, Quality Auditor certifications a plus.
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quality assurance jobs Title: quality assurance intern Company: White Castle in San Jose, CA
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