This position requires access to information which is subject to stringent controls under the International Traffic in Arms Regulations (ITAR) or Export Administration Regulations (EAR).. Applicants must be a U.S. citizen or national, U.S. lawful permanent resident, person granted asylee status in the U.S., or person admitted into the U.S. as a refugee.. Develops, implements and maintains quality control systems and standards, methods and procedures for inspecting, testing and evaluating the precision, accuracy and reliability of company products, ensuring finished products conform to government and company standards and satisfy good manufacturing practices regulations. Provides technical support to the quality assurance and quality engineering functions by conducting inspections on products, materials, components, parts, etc., at various stages of the production process. Uses magnifiers, electronic instruments, calipers, micrometers, snap gauges, HIPOT, automated electrical equipment, and special fixtures and verifies calibration against standards
Join to apply for the Director, Financial Planning & Analysis Supply Chain role at Vuori.. Job Description Reporting to the VP of Financial Planning & Analysis the Director FP&A - Supply Chain will play a key role in leading financial planning, analysis, decision support, and reporting for end-to-end supply chain activities, including product costing, inventory management, and logistics. Support system implementations/enhancements (e.g. ERP, EPM tool). Familiarity Microsoft Office, BI tools a plus (Domo, Power BI).. Apparel industry and experience with Microsoft d365, EPM tools, Shopify a plus.
Assists periodic product audits/inspections on running parts and conduct final shipment audits utilizing AS9100 Standard as the basis for auditing. Proficient in AS9100 Aerospace Standard is a plus, other related quality system standards (e.g., TS16949 etc.. Ability to use precision measuring instruments (Caliper s, Micrometer s, Optical Comparator s, Faro Arm CMM is a plus, Pin Gauges, Drop Gauge, etc). High school diploma with additional technical courses, CQT or CMI preferred. Minimum 5 year Quality Inspector experience in manufacturing and minimum of 2 years of Quality Technician Experience.
The QC Associate I is responsible for routine, accurate and timely testing of QC samples according to standard protocols and operating procedures, such as flow cytometry related protocols.. This may require working with human blood, human or mammalian cell culture and/or animals and animal tissues.. Report problems to QC Supervisor or Manager.. Participate in Environmental, Health & Safety programs.. Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices.
This may require working with human blood, human or mammalian cell culture and/or animals and animal tissues.. Analyze data and report test results including completion of all required documentation and database entries as required by QC protocols or operating procedures.. Report problems to QC Supervisor or Manager.. Participate in Environmental, Health & Safety programs.. Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices.
You will have opportunities to contribute to new product design, customer requests, lab testing, PCB development and troubleshooting.. Strong understanding of NI test stand/LabVIEW architecture & best practices. Interested in power electronics. PCB layout and design via Altium. Previous power electronics experience
Collaborate with Analytical Development for seamless method transfers and onboarding of new assays into the QC laboratory. Bachelor's degree in a relevant Biological Science discipline (Master's or Ph. D. 7+ years of experience in a GMP Quality Control laboratory or GMP/GLP setting. In-depth knowledge of FDA regulations, ICH guidelines, USP standards, and cGMP requirements for cell therapy or biologics. Hands-on experience with laboratory methods including flow cytometry, Real-Time PCR, DNA isolation, ELISA, bioactivity assays, and sequencing.
Title: QC Inspector II. Performs in-process an/ord final inspection on materials, detail components, hardware, and assemblies to ensure product compliance to Customer and Company requirements. Inspects machined parts, components, assemblies and materials to ensure compliance with appropriate regulatory guidelines (Military Standards, ASTM and ANSI, and ASME Codes). Good knowledge of aerospace manufacturing practices, procedures, inspection methodologies, and techniques in an AS9100 QMS environment. Performs in-process an/ord final inspection on materials, detail components, hardware, and assemblies to ensure product compliance to Customer and regulatory requirements by using a variety of measuring equipment with minimal supervision.
Our Operations Team is seeking an on-site Senior Purchasing Agent.. The Senior Purchasing Agent is responsible for executing company policy, processes and procedures to ensure all statutory and regulatory compliance.. You would also be responsible for the development of strategic sourcing partners in alignment with the needs of programs, projects, engineering, finance, marketing and quality assurance in support of the organizational strategic goals including supplier sourcing, supplier negotiations and supplier management.. APICS (CPIM) and/or NAPM (CPM) certification preferred.. Previous experience with ERP/MRP systems, preferably in an electronics OEM environment.
Toyota Carlsbad is seeking a motivated and detail-oriented Quality Control Specialist to join our Service Department team. The Quality Control Specialist will ensure our “Repair Issue Resolution” score consistently meets or exceeds company standards. Conduct daily quality control inspections on randomly selected vehicles to ensure repair standards are maintained. Perform random quality checks and road tests on vehicles near completion to ensure readiness and safety. Understand and promote adherence to the Toyota Express Maintenance process for optimal workflow and efficiency.
Toyota Carlsbad is seeking a motivated and detail-oriented Quality Control Specialist to join our Service Department team.. The Quality Control Specialist will ensure our “Repair Issue Resolution” score consistently meets or exceeds company standards.. Conduct daily quality control inspections on randomly selected vehicles to ensure repair standards are maintained.. Perform random quality checks and road tests on vehicles near completion to ensure readiness and safety.. Understand and promote adherence to the Toyota Express Maintenance process for optimal workflow and efficiency.
Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability.. These markets include aerospace and defense, factory automation, environmental monitoring, electronics, oceanographic research, oil and gas exploration, medical imaging, and pharmaceutical research.. We are currently hiring for an R&D Laboratory Technician.. Maintain complex test equipment, including calibration and preventive maintenance scheduling.. Teledyne is committed to ethical business practices and equal employment opportunity, considering all qualified applicants without discrimination based on race, gender, age, disability, or other protected characteristics.
This may require working with human blood, human or mammalian cell culture and/or animals and animal tissues.. Analyze data and report test results including completion of all required documentation and database entries as required by QC protocols or operating procedures.. Report problems to QC Supervisor or Manager.. Participate in Environmental, Health & Safety programs.. Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices.
Toyota Carlsbad is seeking a motivated and detail-oriented Quality Control Specialist to join our Service Department team.. The Quality Control Specialist will ensure our “Repair Issue Resolution” score consistently meets or exceeds company standards.. Conduct daily quality control inspections on randomly selected vehicles to ensure repair standards are maintained.. Perform random quality checks and road tests on vehicles near completion to ensure readiness and safety.. Understand and promote adherence to the Toyota Express Maintenance process for optimal workflow and efficiency.
Responsible for leading and developing drug supply planning strategy and overall management of all aspects of drug supplies (IP) for global Phase I - III clinical studies as the leader of Investigational Medicinal Supply Chain (IMSC).. Coordinate drug supply delivery timelines with Clinical and CMC; Packaging, Labeling, and Distribution CRO's; and indirectly with GMP manufacturers, QA, and Regulatory Affairs,. Support financial planning for global clinical supplies, including budgeting, forecasting, and strategic planning activities for clinical trials; and reconciliation of drug distribution invoices with finance staff to maximize productivity, efficiency, and overall business performance.. Fundamental knowledge of inventory management and forecasting systems, IVR systems, and Clinical Trial Supply processes is required.. Collaborates with Quality Assurance, cGMP and cGCP Compliance Specialists and Subject Matter Experts, and maintains a strong understanding of Global Health Authority regulations for packaging, labeling, systems, distribution, and vendor management is required.
Ignite your career at Builders FirstSource, America’s largest supplier of building materials, value-added components and building services to the professional market.. At BFS, you’ll be equipped with all the tools, training, and resources you need, and you’ll be empowered to try new things, gain new experiences, and build a career with unlimited horizons.. Compiles data from records and shipping/receiving documents, requisitions, contracts and accounting reports.. At BFS, we want you and your career to be greater than what you ever could have expected.. Our supportive, people -first culture will build you up and empower you to do more, be more, and become better every day.
This may require working with human blood, human or mammalian cell culture, and/or animals and animal tissues.. Report problems to the QC Supervisor or Manager.. Participate in Environmental, Health & Safety programs.. Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices.. Flow Cytometry experience required, and Tissue Culture experience highly preferred.
The Senior QC Analyst is responsible for executing quality control activities, including in-house environmental monitoring and water testing, final release and stability testing, and incoming quality inspections.. The Senior QC Analyst also facilitates outsourced testing and contributes to maintaining an efficient and compliant QC laboratory.. Conduct high-purity water testing in accordance with USP. Support functional assay development and validation in collaboration with R&D and manufacturing teams.. Experience with environmental monitoring, water testing, and microbiological/chemical testing methodologies preferred.
Manage onshore/offshore team that provides level 2/3 support activities of Workday managed services engagements for a variety of post-production clients including enhancement and optimization initiatives, break/fix support, release management, new feature deployments, process improvement and road mapping activities. Operate as Supply Chain Management lead for all managed services engagements acting as the point of contact for escalations and work prioritizations; ensure client satisfaction and timely delivery and collaborate with clients to strategize and drive goals forward post-production. Assist with onshore/offshore resource management, forecasting, and load balancing; assess skill levels and gaps and upskill team members as needed; identify strategies, risks, and opportunities to meet client needs and grow/improve the team. Lead SCM pillar by mentoring a team of Workday Supply Chain consultants; provide guidance, coaching, and support for team members; act as functional subject matter expert during sales and proposal activities as well as on KPMG Value Optimizations, assessing tenant to identify optimization opportunities for clients to realize value out of Workday investment. Minimum five years of recent experience in post-production, managed services support or consulting experience working directly with internal/external clients in area of Workday Supply Chain Management; minimum two years of recent experience in a leadership role
Under minimal supervision, the Quality Technician I is responsible for, but not limited to, conducting inspections of materials, components, subassemblies and finished products in accordance with company procedures to meet customer expectations.. Collect and record Key Performance Indicator (KPI) data and prepare associated reports. Collect and record Statistical Process Control (SPC) data and prepare associated reports. Good data collection and analysis skills with strong attention to details.. Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.