This strategic role demands deep expertise in Source to Pay processes, including requisition to approval, PO management, contract lifecycle management (CLM), guided buying, catalogs, and services procurement systems such as SAP and Ariba.. The ideal candidate will be responsible for enabling cross-functional collaboration, aligning future-state STP designs with goals of process standardization, data quality improvement, and technological innovation.. Act as a recognized subject matter expert (SME) in Source to Pay (STP) , representing procurement teams and stakeholders in the S/4HANA modernization program.. Lean Six Sigma Green Belt certification.. Lean Six Sigma Black Belt.
Work closely with the Branch Manager to forecast equipment needs and coordinate repairs or maintenance. Assist with workforce planning, including recruitment and scheduling of staff based on operational needs. Collaborate with the Branch Manager on strategies for cost reduction and operational efficiency. Familiarity with fleet management and scheduling tools. As the nation’s leader in concrete cutting, coring, scanning, and demolition, and ranked 3rd in Demolition by ENR's 2023 Top Specialty Contractors, we deliver more than just expertise—we deliver results.
The Director of Quality Systems will play a key role in supporting this subsidary of one of the largest medical device companies in the world. There extensive experience in quality systems will be a needed in helping grow this medical device company. Oversee and maintain quality systems, including change control, CAPA, document control, and risk management processes (e.g., FMEA). Knowledge of supplier quality management and lean manufacturing principles. Certifications such as CQE (Certified Quality Engineer) or Six Sigma Green Belt/Black Belt.
The VP of Operations is critical to Fellow's success, leading and optimizing all key operational functions.. Supply Chain Management: Oversee the end-to-end management of Fellow's global supply chain, including sourcing, procurement, production, and logistics.. Oversee quality control processes throughout the supply chain, from raw materials to finished goods.. Logistics and Fulfillment: Optimize logistics operations to ensure efficient and timely order fulfillment.. Masters Degree or MBA preferred.
Initiate, plan and author engineering change orders to product design, product documentation, Bills of Materials, manufacturing/test/packaging procedures, process routings, tooling, compliance (EMC, safety, laser safety, ROHS, UDI etc. Broad experience supporting many of the following commodities or supplier types: lasers, optical components, fluidic systems, machined parts, sheet metal, cables, PCA's, plastics, power systems, product packaging, turnkey subcontractors, hardware, labeling.. Staff Manufacturing Engineer (Automation Experience Required)Senior Manufacturing Wire Harness Engineer.. Senior Electronics Manufacturing Engineer (Harnessing and Electronics)Senior/Staff Power Electronics Manufacturing Engineer.. Senior Mechanical Engineer – Interconnect DesignSenior Electro-optic Assembly Process EngineerSr. R&D Engineer (Process Development) - ShockwaveSr. Manufacturing Engineer, Cell Electrode
The area of Materials Services spans two strategic areas: global materials distribution as one-stop-shop - from steel and stainless steel, tubes and pipes, nonferrous metals and specialty materials to plastics and raw materials - and tailored services in the areas of materials management and supply chain management.. Services include supply chain management, logistics management, testing and inspection services, and packaging and kitting.. These may include: recruitment; training and development; compensation/remuneration; performance evaluation; organizational development; relocation; equal employment/affirmative action; human resources administration; human resource information systems; employee communications; employment/industrial/labor relations.. This position works on site in a warehouse / manufacturing environment in Livermore, CA. This role is not eligible for hybrid or remote.. SPHR Certification or SHRM-SCP Certification
Conducting process / operator audits within the above stated departments to determine if variations to the procedure have been introduced.. - Bachelor's or Master's degree in Chemical Engineering or 3-5 Years related experience in Process Engineering, or in a PCB manufacturing.. As such, all applicants must be U.S. persons, as defined by ITAR (U.S. citizens, U.S. lawful permanent residents, or individuals with refugee/asylee status).. The company features 6 total manufacturing sites: Santa Clara, our headquarters in the heart of the Silicon Valley; 2 in Southern California, 1 in Maple Grove, Minessota, Aurora, Colorado and Chandler Arizona.. of manufacturing space with over 480 employees, making AdvancedPCB one of the largest privately held printed circuit board manufacturers in North America.
Our ~15,000 employees create world-class solutions in communications, 5G, automotive, energy, quantum, aerospace, defense, and semiconductor markets for customers in over 100 countries. This role will be to manage critical supplier relationships focused on high mix / low volume electronics manufacturing within our vertically integrated Semiconductor fabrication operation and external Foundry portion of Keysight’s supply chain. You may also participate in or lead process improvement efforts in areas such as NPI, resourcing, cost reduction, and quality. BS/BA degree, or similar experience, in supply chain management, business, international business, finance, or another related field. 7-10 years experience in Supplier Management or Commodity Management with an extensive track record of results.
Redwood Materials was founded in 2017 to create a circular supply chain for electric vehicles and clean energy products, making them more sustainable and driving down the cost for batteries. Manufacturing Test Engineer, Energy Storage.. Work with firmware & software teams to develop test automation, self-test, and data analysis.. Bachelor's degree in Mechanical Engineering, Electrical Engineering, Mechatronics, or a related field.. Ability to perform the essential job functions consistent safely and successfully with the ADA, FMLA and other federal, state and local standards, including meeting qualitative and/or quantitative productivity standards
Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.. Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people.. The Senior Director works internally with other members of Global Supply Chain (GSC) and other Gilead functions – e.g., Clinical Development, Clinical Operations, Product Development & Manufacturing (PDM), Quality Assurance, Regulatory, and Project Management Office - to develop and formulate supply chain strategies, meet project deliverables, solve business problems and create competitive advantage.. Expertise in clinical supply management experience, knowledge in forecasting, demand & supply planning, IRT systems, inventory management, clinical labeling, distribution including cold chain, import & export, reverse logistics, CMC and GxP regulations. Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences.
At Persimmons, Inc., we are pioneering the future of generative AI with our ground-breaking full-stack innovations, including hardware and software integration capable of supporting trillion-parameter models.. We envision the future of AI hardware with our cutting-edge generative AI solutions designed for edge computing and hyperscale cloud environments.. Oversee the daily operations of the company, including production, logistics, supply chain, and customer support.. Bachelor’s degree in Business Administration, Operations Management, or a related field; MBA or advanced degree preferred.. Experience with supply chain management, production planning, and logistics.
You will work alongside our R&D Engineering teams and CM factories to develop and ramp NPI programs, supporting the mission critical goal of quality and quantity.. Drive cost optimization initiatives through process improvements, lean manufacturing principles, and efficient resource allocation to minimize MVA (Manufacturing Value Add). Contribute to supply planning and manage capacity planning for the region. 7+ years of experience managing prototype builds, ramp-ups and mass production of consumer electronics products in a high volume NPI Development Cycle. 5+ years of experience managing Supply Chain and Contract Manufacturer pricing and MVA
Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.. Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people.. The Senior Director works internally with other members of Global Supply Chain (GSC) and other Gilead functions – e.g., Clinical Development, Clinical Operations, Product Development & Manufacturing (PDM), Quality Assurance, Regulatory, and Project Management Office - to develop and formulate supply chain strategies, meet project deliverables, solve business problems and create competitive advantage.. Expertise in clinical supply management experience, knowledge in forecasting, demand & supply planning, IRT systems, inventory management, clinical labeling, distribution including cold chain, import & export, reverse logistics, CMC and GxP regulations. Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences.
Hiring Production Planner that will work as part of the program management team to integrate procurement, logistics, supply chain and manufacturing to affect efficient material flows from order entry to fulfillment. The Production Planner will perform facilitate cross-functional and multi-level discussions, analyze future production requirements, and assist this Program Management team as needed Responsibilities Include: Apply SIOP (long-range, demand, supply, capacity planning) to all areas of operations and participate in review discussions. Create and Maintain SAP BOM and recipe load files. Analyze future production requirements which may include workforce planning strategies to develop recommendations to ensure machine load and work force can meet the production requirements. Strong regard for product safety and quality standards.
Founded in 1991, we've grown into a leading provider of electronics manufacturing services (EMS), offering a comprehensive suite of solutions from design and manufacturing to supply chain management.. The Planner 3 plans, schedules, and coordinates the efficient movement of material through the production cycle, creates and manages work orders and is responsible for materials data input and integrity to effectively manage delivery and inventory costs.. Manage Project Master Production Scheduling (MPS) from Demand to Ship. Maintain and plan work orders accordingly to meet OTD objectives.. Provide information to Program Manager (PM), Supply Chain Management (SCM) & Buyer for constraint materials and/or manufacturing issues if any.. Have in-depth understanding of how backend operation works from sourcing, purchasing, tracking PO, receiving, IQC, warehousing, kitting, SMT, and system integration to close the cycle of work order completion.
The role ensures adherence to cGMP standards, supports quality initiatives, and contributes to efficient production processes under limited supervision.. ^Execute logistics coordination, batch record documentation, equipment use logs, and work order initiation and tracking.. ^Assist in project support and creation/maintenance of training kits and documentation.. ^Ensure all work is conducted in compliance with cGMP and cGDP guidelines.. ^Maintain personal training compliance and provide training to other technicians upon qualification.
Use the Discrepancy Management system/database and RCA tools at an expert level for investigations, data entry, and data mining;.. Solid understanding of pharmaceutical operations within clinical and commercial manufacturing, QC, Supply Chain, Validation, and Quality Systems. Knowledge/experience with risk assessments, regulatory document review, audits, Lean Six Sigma, and continuous improvement methodologies is preferred. Hands-on experience with pharmaceutical manufacturing processes, equipment, utilities, and facilities, including cGMP compliance and high purity water systems. Proficiency with Microsoft 365, SAP, MES, JMP, Veeva, ValGenesis, and other relevant systems.
Compensation & Benefits: HIRING SALARY RANGE: $50.00 - $74.00 (Salary to be determined by the education, experience, knowledge, skills, and abilities of the applicant internal equity, and alignment with market data.). Monitors and/or manages the entry of correct documentation and scheduled maintenance via Maximo/SAP.. Experience in a leadership position demonstrating the ability to analyze Facilities Maintenance related problems (e.g. Electrical, Mechanical, HVAC, Cranes and Hoists, etc.). Experience creating metrics and data mining for driving performance results.. Experience utilizing Continuous Improvement disciplines such as Six Sigma, Kaizen, Lean Manufacturing, 5S, 4 M's, etc.
The Medical Materiel Specialist III shall include but are not limited providing supervision and overall operational responsibility for medical logistics functions to include advanced medical supply chain activities and biomedical equipment maintenance functions.. Oversee medical supply chain operations, including procurement, inventory management, storage, and distribution of medical materiel.. Expertise in medical logistics, supply chain management, and biomedical equipment maintenance.. Specialized experience shall include supervision and overall operational responsibility for medical logistics functions to include general medical supply activities, ordering, receiving, customer support, inventory management, warehousing and operation of various materiel handling equipment, report development, analyzing log functions, and biomedical equipment maintenance functions.. Experience shall have taken place in a healthcare or healthcare support setting and have a comprehensive understanding of medical WRM, FHP,and IMAHR program management and ECMM operation execution of Class VIII medical supply sustainment.