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Position Title: CNC Programmer Department: Model Shop/Engineering Location: Fenton, MO Reports To: Manufacturing Engineering Manager/Machine Shop Manager Classification: Hourly - Non-Exempt Schedule: Tuesday - Friday - 5:00 am - 3:00 pm Position Summary: Launch newly developed offline programming department to improve overall CNC throughput, quality, and process standardization.
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Experience with 8Ds, corrective action, and preventive action programs; required LICENSING/CERTIFICATIONS: ASQ Certification (Quality Auditor, Quality Engineer, Quality Improvement Associate); preferred COMPETENCIES KNOWLEDGE: Quality - Knowledge of tools, SPC, concepts and methodologies of QA. Manufacturing - Knowledge of production processes, costs, quality control, raw materials and other methods for maximizing the efficient manufacture and distribution of goods.
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Detailed understanding of quality process and procedures, to include experience with Lean Manufacturing, ISO, SPC, and computer-based analytical/reporting tools is required. This includes providing oversite to the quality team, defining quality requirements, preparing documentation (including control plans, PFMEA's, PPAP's, and corrective action), and monitoring production quality performance to find opportunities for improvement.
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This position will work closely with CMC Analytical Development and CMC Quality Control, Regulatory Affairs, and other functional teams. Reporting to our Senior Manager, Quality Assurance CMC, this position is responsible for managing, reviewing, and approving quality documents from Contract Manufacturing Organizations and Contract Testing Laboratories for manufacturing, testing, validation, and disposition of clinical and commercial products for human use.
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The QA Documentation Specialist is responsible for developing, implementing, and maintaining end-to-end Quality Assurance document systems at Chemical Guys. We manufacture our auto-detailing chemicals right here in Carson, CA and this is a great opportunity to grow and work alongside our both our quality (QA/QC) and manufacturing teams.
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Provide day-to-day Quality support of the warehouse, manufacturing, packaging, and batch record review areas. 5+ years of work experience in Quality Assurance or Regulatory Affairs in a cGMP pharmaceutical and/or biological manufacturing regulated environment preferred.
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Monitoring of FSQA programs including HACCP Program, sanitation standard operating procedures, pest control, good manufacturing practices, approved supplier program, foreign material control, plant sanitation, chemical control, product quality assurance, FSQA Customer complaints, food defense and security.
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Flow cytometry, method validation, qc, analytical skill, R&D, Quality control, Validation, Analytic, Gmp, Laboratory, method development. This includes leading projects in process development, technology transfer and continuous improvement of our client's novel manufacturing processes.
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As a Supplier Quality Manager , you will be leading, inspiring, and setting strategic quality direction for our contract manufacturing partner and a team of Mfg Quality Engineers who ensure quality control and issue prevention throughout the new product introduction, manufacturing, and delivery phases for contract manufacturer operations building our award-winning Monarch Tractor.
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Demonstrated success leveraging Advanced Quality Planning Tools such as DVPR, PPAP, statistical process control, control plans, FMEA, building inspection and production quality plans.
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Requirements: ISO9001/ Quality Control/ Plastics Industry/ AS9100. A minimum of 3 years of experience in a Quality Manager role within the Manufacturing Industry. Proven experience with Quality Control, Quality Assurance, and Process Improvement.
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As our Quality Control Lead you will assist in overseeing QC Technicians to ensure a smooth workflow throughout our QC department. Quality Control Lead-Onsite Position. Quality Control Lead.
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The incumbent will work cross-functionally with colleagues from Manufacturing, Manufacturing Science and Technology, Global Engineering, Validation, Process Engineering, EM/UM Quality Control, CMC Regulatory, and Quality Operations on the design of processes and technologies required to produce aseptic drug product to successfully commercialize an exciting and diverse portfolio of innovative cell and gene therapy pipeline programs.
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Strong oral communication skill and demonstrated technical writing skills: able to write detailed reports, comprehensive manufacturing procedures and assist Quality Engineering with validation protocols.
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Collaborate with cross-functional teams including Product Design, Manufacturing, Quality and Product Operations to deliver products to customers. Use statistical process control and studies to validate process capability, establish reasonable specifications, and drive process improvements in partnership with Tooling and Manufacturing Process Engineers.
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