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Job Title: Quality Systems Engineering Manager. Experience in semiconductor or electronics manufacturing industry in the functional areas like Quality Management Systems and audits.
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Oversee the implementation and monitoring all tracking systems related to data reporting requirements. Rehab Systems Management Provides supervision in all areas of the Day Hab Systems reporting standards to ensure organizational compliance with all DMA, DDS regulations.
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Experience with the use of quality systems and tools (for example, CAPA, Six Sigma methodology, change control, Statistical Analysis, Control Plans, and document management) Manager, Quality Systems Engineering - Medical Products page is loaded.
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Collaborate with cross-functional teams, including the CDMO joint project team, Obsidian Process and Analytical Development, Quality Assurance, Quality Control, and Regulatory to assure effective tech transfers and start-up of new manufacturing processes according to agreed upon timelines in support of business objectives.
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In the past decade, as the fields of proteomics and metabolomics have developed as leading techniques for determining biomarkers for disease presence, progression and the monitoring of therapeutic response, CIL has worked closely with industry leaders and researchers to provide the stable isotope-labeled tools needed for improved quantitation and qualification of complex biological systems.
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Since the systems SDD develops are deployed in operationally relevant environments, the hardware you develop needs to meet standards of quality, maintainability, and reuse. Understanding of and experience with RF systems and their principles of design, development, requirements verification, test planning, test execution, and data analysis.
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The Senior Analyst / Scientist will work cross-functionally with others in Quality Control, Analytical Development teams, Quality Assurance, and Manufacturing, as needed. The Senior Analyst/ Scientist, Quality Control Chemistry, will support external laboratory testing and internal study protocol design, study report review and IND support as needed.
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Required Technical Skills: Operating Systems: Red hat Enterprise Linux, Solaris and VMware Hardware: Dell Software/applications: RedHat IDM, McAfee; Enterprise Central Logging, LDAP, Splunk, NetApp, VMware vCenter/ESXI/vSAN, GitHub, ACAS Networking applications and protocols: TCP/IP, DNS/DHCP, NTP, SSH Programming Languages: Ansible, Shell Scripting, PowerShell.
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Leadership in areas of Lean Manufacturing, KAIZEN, ISO quality systems, innovation, and current systems technology. + Preferred: Experience with Lean Manufacturing and ISO quality systems.
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Triton is developing subsea systems, submarine systems, unmanned undersea vehicles (UUVs), sonobuoy, towed array, and offshore renewable energy. Experience designing systems for submarines, or other subsea applications.
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Experience with IT and/or network and system security administration, including operating system security configuration and account management best practices for UNIX, MS Windows, Red Hat Enterprise Linux, and CISCO systems.
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As the Director of IT for Manufacturing Operations and Supply Chain, you will be responsible for leading the strategic direction, implementation, management, and optimization of all technology solutions supporting Manufacturing and Supply Chain operations within the organization with a primary focus on SAP and Oracle E-Business Suite (EBS) as well as several key Manufacturing, Quality Assurance and Export Compliance systems.
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Participate in project kick-off teams improving quality aspects of product introduction, and have a fundamental understanding of quality systems, SPC, and control plans. Support quality improvement efforts, Internal Auditing and Continuous Improvement initiatives.
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Strong typing and computer skills, including efficiency using Microsoft Office Suite (Word, Excel, PowerPoint), and familiarity with cGMP quality systems - Veeva, Theia, LIMS, IDBS.Operate as a part of a team with experience supervising and or training individuals in a functional, safe working environment while maximizing laboratory efficiency.
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Record and review GMP data, monitor and evaluate QC systems and equipment, recommend improvements to procedures, and revise GMP documentation as required. Oversee and continuously improve FDA / regulatory compliant Quality System for QC laboratory system.
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quality tech systems jobs Title: senior data scientist in Billerica, MA
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