Collecting information
Organizing data
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.
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
The candidate is expected to lead and oversee all Operations for the company, including customer installations and deployments, customer interface management, SLA monitoring and maintenance, field operations, continuous improvement, and supply chain development and procurement.. The Head of Operations will also serve as the key interface between Engineering and the field, providing feedback for technology enhancements, prioritization and resource allocation.. Ability to grasp and manage complex customer delivery pipeline that integrates hardware, software and customer workflows is a must.. Ardent customer advocate with heavy focus on customer delight; capable of understanding and focusing on customer value derived from Vimaan’s products.. Strong practitioner of traditional Quality Management tools and Six Sigma processes, including SQC and CAPA processes.
We're backed by investors like Kleiner Perkins, Construct, Bloomberg BETA and Promus Ventures.. We have a great team, where you will be surrounded by talented engineers and tech leaders from companies like Cruise, Zoox, Google, Verb Surgical, Tesla, Nuro, Vicarious, Amazon Robotics, Strateos, Built Robotics, Facebook, Plenty, Yelp, and Microsoft.. As the Senior Robotics QA Automation Engineer, you will assume technical leadership in the design and implementation of automated test frameworks.. Implement HMI interface automation to ensure thorough validation of operator interactions with packaging systems.. Experience with industrial automation or manufacturing systems.
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
Design and launch greenfield and brownfield production lines for data center equipment and rack system assembly.. Drive continuous improvement through lean manufacturing, Six Sigma, and simulation-based process modeling.. Coordinate with Construction, Logistics, Data Center Operations, and Sourcing to align factory output with deployment schedules.. Have led the launch of at least one complex, low-volume production line (e.g., enclosures, switchgear, or electromechanical assemblies).. Understand data center infrastructure and how upstream factory decisions affect site-level deployment.
Design and launch greenfield and brownfield production lines for data center equipment and rack system assembly.. Drive continuous improvement through lean manufacturing, Six Sigma, and simulation-based process modeling.. Coordinate with Construction, Logistics, Data Center Operations, and Sourcing to align factory output with deployment schedules.. Have led the launch of at least one complex, low-volume production line (e.g., enclosures, switchgear, or electromechanical assemblies).. Understand data center infrastructure and how upstream factory decisions affect site-level deployment.
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
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
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.
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 responsibilities of the Maintenance Mechanic for the food manufacturing company are. Perform routine preventative maintenance on manufacturing and packaging equipment (e.g., blenders, mills, tablet presses, encapsulation machines, labelers, cappers, bottle fillers).. Assist with calibration and monitoring of systems like compressed air, HVAC, and water purification.. High school diploma or GED required; technical training or certification in mechanics, mechatronics, or related field preferred.. 3+ years of maintenance experience in a GMP-regulated manufacturing environment (nutraceutical, pharmaceutical, food, or cosmetics).
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.
The candidate is expected to lead and oversee all Operations for the company, including customer installations and deployments, customer interface management, SLA monitoring and maintenance, field operations, continuous improvement, and supply chain development and procurement. The Head of Operations will also serve as the key interface between Engineering and the field, providing feedback for technology enhancements, prioritization and resource allocation. Ability to grasp and manage complex customer delivery pipeline that integrates hardware, software and customer workflows is a must. Ardent customer advocate with heavy focus on customer delight; capable of understanding and focusing on customer value derived from Vimaan’s products. Strong practitioner of traditional Quality Management tools and Six Sigma processes, including SQC and CAPA processes.
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.
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.
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.
Participate in process and laboratory improvements, such as development of procedures and studies (i.e. 5s, Kaizen, Six Sigma) and execution of protocols, method validations, and other assay developments. Bachelor's Degree Biology, Microbiology, or other life science; A minimum of 8+ years' experience working in a QCM laboratory or similar GMP setting:Or equivalent combination of education and experience. Experience identifying, authoring, and supporting OOS and DRs. Generally, this job is performed in a clean laboratory setting and routinely uses standard medical and research equipment such as centrifuges, biosafety cabinets, microscopes, incubators, pipettes and computers. As a full-scale CDMO, we provide customers with services for the development and manufacturing of lentiviral vectors and cell and gene therapy products.
Microbiologist II *PC. Participate in process and laboratory improvements, such as development of procedures and studies (i.e. 5s, Kaizen, Six Sigma) and execution of protocols, method validations, and other assay developments. Bachelor's Degree Biology, Microbiology, or other life science; A minimum of 8+ years' experience working in a QCM laboratory or similar GMP setting:Or equivalent combination of education and experience. Generally, this job is performed in a clean laboratory setting and routinely uses standard medical and research equipment such as centrifuges, biosafety cabinets, microscopes, incubators, pipettes and computers. As a full-scale CDMO, we provide customers with services for the development and manufacturing of lentiviral vectors and cell and gene therapy products.
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.