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The role works closely and have high visibility with Executives, VP's and Directors of Engineering, Infrastructure, SRE, Product Management and Customer Support to ensure overall software quality in development pipeline all the way to production regions, and to set the strategy for developing high-quality software to solve complex problems for our customers and users.
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The Software Quality Assurance Testing Engineer will play a key role in the quality assurance of Anti-Money Laundering ("AML"), Sanctions Screening, AML Transaction Monitoring, and Know Your Customer ("KYC") suite of applications in the Boston, MA area.
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We are willing to invest time, money and resources into teaching and training someone to assemble high quality bikes in a fun and fast-paced environment. Our power equipment department is known for expert repairs and sales of products from leading manufacturers including Honda, Stihl, Ariens, Toro, Redmax & Ego. We stock a complete selection of lawnmowers, snowblowers, chainsaws, trimmers, generators and more.
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Minimum of 10 years of progressive quality experience; including experience in a QA leadership role in the related field or a combination of equivalent education and relevant experience along with at least 5 3 years of supervisory/management experience.
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All-around training in all areas of tool making and conventional soft machining, CNC Machining, hard machining, heat treatment, precision grinding, precision ram EDM, precision wire EDM, mold making, die making, electrode manufacturing, proto-typing, machine assembly and debug, planning, quality and metrology.
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Serve as the focal point for all quality, clinical, survey and certification, and policies for MassHealth ACO, MCO and CP models. Develop, test, evaluate, adopt and support performance measurement systems (i.e., quality measures and health equity initiative) to evaluate care provided to MassHealth members enrolled in ACO models.
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Vor Bio is seeking an experienced Quality Control Senior Analyst to be a part of the team responsible for the day-to-day operations assigned to the QC Microbiology group, including sampling of a cGMP manufacturing facility, testing samples in the QC Microbiology laboratory for batch release of advanced therapeutics including cellular and gene therapy products.
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The CLIA Quality Manager will collaborate with direct and/or delegated authority to ensure the CLIA Quality Management Systems (QMS) are effective and compliant with applicable requirements, provide leadership and guidance re: CLIA and associated regulations, and support the Lab Director and leadership in maintaining audit readiness.
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The Radiologic Technologist/Mammographer is expected to produce high quality Radiographic and mammographic images under the guidance of the Radiology Supervisor. The Radiologic Technologist/Mammographer will also take part in Quality Improvement and Quality Control activities.
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The selected candidate will also work collaboratively with Quality Assurance to assess laboratory conformance with cGMPs, and with CMC Regulatory Affairs to ensure the translational accuracy and integrity of data incorporated into Module 3 sections of CTD regulatory submissions and written responses to regulatory authorities.
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You will build high quality, robust, and efficient analytical solutions that will be used to improve Fixed Income's investment processes. We build high quality, robust, and efficient high-responsive solutions that are used to improve efficiency and decision-making processes.
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Partner with CMC Regulatory and SMEs to assess compliance with regulatory guidelines and industry best practices for US and EU markets to ensure appropriate quality processes and procedures are implemented for commercial cell-therapy GMP manufacturing, at-scale and in-compliance.
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Must have strong knowledge of biologics and small molecules manufacturing, materials management, quality control, quality assurance and CMC regulatory requirements. Responsible for all aspects drug substance including conjugation process development, validation, characterization, scale-up, tech transfer, analytical method qualification, specifications, release and stability testing.
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The Senior Director, GCP Quality Assurance coordinates GCP Compliance activities with Clinical Operations, Regulatory Affairs, Clinical Supply & Logistics, Sample Management and Pharmacovigilance as well as vendors supporting Scholar Rock sponsored Clinical Studies.
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CFS is seeking an experienced Quality Inspector to lead inspection and test activities for the SPARC project. Interface with Technicians on issues related to quality and help them in understanding and interpreting quality specifications and technical drawings.
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quality job Title: field tech Company: Dhl in Jamaica Plain, MA
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