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Within TDS, the Analytical Development (AD) Biologics group supports method development and validation, process and formulation development, release, and stability analytics via automated workflows.
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The Lead Mechanical Design Engineer will be part of the LEAP Engineering Design Team in Cincinnati, OH. They will refine technical expertise and leadership skills by working turbomachinery design and product improvement activities that ultimately power our customers, lift people up and bring them home safely.
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The QA Specialist conducts QA audits of BIO laboratories and functions including but not limited to ongoing process, data review audits, technical report, and study independent facility / process.
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Provide manufacturing/process engineering support for printed circuit board assembly line. Provide manufacturing/process engineering support for cable/harness assembly, chassis assembly and final unit assembly.
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This position is responsible for exceeding sales and operational benchmarks, delivering an exceptional customer experience through the La-Z-Boy selling process, and championing the in-home design program.
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Focus on continuous process improvement and identify opportunities for automation, fusion of disparate sources of security findings, and consistency of remediation owner experience. Experience with Aqua, Palo Alto Prisma, Wiz, CrowdStrike, Tenable Nessus, or Qualys preferred.
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Provide data for process safety key performance indices and propose improvement actions and recommendations accordingly. Process Safety Engineer - Exton, PA (On-Site) The Process Safety Engineer will review all new proposed processes, process equipment, proposed changes to processes or process equipment, and existing plant operations to determine all necessary SHE (Safety, Health & Environmental) requirements are addressed in a thorough and rigorous manner.
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Lead Kaizen and process improvement events and follow-up audits to ensure sustainment and completion of parking lot items. Partner with site management team to identify, scope and coordinate process improvement events.
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Manage the LIMS change control process through timely resolution of incident tickets. One of our large pharmaceutical clients is looking to hire a QC Lab Analyst -Systems Specialist to support the QC Clinical, Release, and Stability (CRS) Laboratory, Laboratory Method Execution (LME) project and is responsible for local systems management in the QC organization and communication with global workgroups within the systems area.
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Skills in process analysis, assessment and improvement as well as creating a team environment where continuous improvement is encouraged. Payroll Operations lead has primary responsibility for all aspects of payroll operations processing, including ADP payroll BAU process deployment to ensure a consistent focus and involvement in driving efficiencies and process improvements.
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Quality Control Specialist-Large Molecule Exton, PA (Corporate) Frontage Laboratories Frontage Laboratories is a CRO / Clinical Research Organization providing integrated, science-driven, product development services throughout the drug discovery and development process to enable life science companies to achieve their drug development goals.
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The Clinical Nurse 2 or Clinical Nurse-NCL demonstrates within the competency domains of Continuous Quality Improvement, Evidence Based Practice and Research, Leadership, Person and Family Centered Care, Professionalism, Safety, Technology/Informatics, and Teamwork.
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CertainTeed is seeking a talented, and energetic senior-level process engineer to lead asphalt innovation research in a growing Roofing R&D team. Interact with asphalt or raw material planners, purchasing, R&D, engineering, and site plant management in support of supply chain forecasting, asphalt supply flexibility, and asphalt process optimization.
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Your expertise in the banking sector, coupled with your proficiency in business process automation with Salesforce, nCino, and other relevant technology will be instrumental in driving our sales and operations team's effectiveness and efficiency.
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The Sr Director, Regulatory Affairs CMC is responsible for identifying and evaluating CMC issues associated with product development including product and process development, device development, analytical methods, formulation development, manufacturing, and labeling.
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process improvement jobs Title: improvement analyst Company: Technologies in Exton, PA
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