- Manufacturing Engineering Manager (Hagerstown, MD)on January 21, 2021 at 4:54 pm
Manufacturing Engineering Manager(Hagerstown, MD) SNAPSHOT! Looking to join a growing organization that is acquiring companies and in need of future leaders? READ ON!! In this position, you will develop and implement optimal, cost-effective fabrication processes and methods in accordance with product specifications and quality standards. Participate in any manufacturing launch for new or revised metal fabricated products. Develop equipment and/or tooling to aid in the manufacturing process. Review, evaluate, improve and implement routings, programming and manufacturing engineering changes to maintain proper product functionality as well as cost efficiency. Recommend and implement improvements to production processes, methods and controls. Immediate opening for a Manufacturing Engineering Managerin Hagerstown, MD who possesses: Requires knowledge in CNC Machining, Sheet Metal Fabrication, Welding, metal chemical surface treatments, assembly, tooling design, molding. Strong knowledge of the manufacturing processes, procedures and CNC milling/lathe equipment. Requires experience with AutoCAD, ProE, Virtual Gibbs, 3D modeling, Mastercam, Featurecam or similar programs related to CNC machining and/or fabrication Strong knowledge and demonstrated experience of Continuous Improvement Practices Strong presentation and training skills required. Strong listening and conflict resolution skills required. Ability to organize and prioritize work. Must have the ability to make recommendations to effectively resolve problems or issues, by using judgment that is consistent with company standards, practices, policies, procedures, including disciplinary issues, regulations and/or labor law. Ability to work well with others and in a team environment. Key Responsibilities include: Coordinate the fabrication launch of new/revised products including establishing production process, sequence of operations, routings, work instructions, equipment and tooling required to produce a quality product that meets customer’ specifications in a cost-effective manner. Improve CNC programs and routings to run more efficiently in the machines to increase overall productivity and throughput. Responsible for leading and driving activities to achieve improvements in the operations of the plant, that lead to positive performance and financial impacts. Manage and develop Key Performance Indicators that drive the improvement activities and create daily accountability. Report on daily performance selected KPIs. Design, develop and test and/or source and cost-justify various tools, machinery and equipment for recommended fabrication methods. Confer with vendors to determine product specifications and arrange for purchase of machinery and equipment according to specifications and quality standards. Confer with management, engineering, manufacturing, opex and other staff regarding manufacturing capabilities, production schedules, and other considerations to facilitate production processes. Confer with design engineering, production and opex staff concerning product design for manufacturability and required tooling to ensure efficient production methods and quality results. Apply statistical methods and perform product/process analysis for cost reduction, quality improvement, and improved efficiency. Employ Lean Six Sigma methodologies and tools in order to accomplish business objectives Perform other related duties as assigned. For immediate consideration, please send your resume to email@example.com!
- Senior Manufacturing Engineer (Carlsbad, CA)on January 21, 2021 at 4:31 pm
Senior Manufacturing Engineer (Carlsbad, CA) SNAPSHOT! Looking to join a technology-driven company headquartered in Carlsbad that has been around for 20 years and has no signs of slowing down? READ ON!! The Quality Manager will be a leading designer, developer, manufacturer and marketer of innovative medical devices used in spinal surgical procedures. Our client combines leading medical device technologies, biologics and instrumentation to create positive surgical outcomes that exceed surgeon and patient expectations. The company markets a complete portfolio of advanced spinal implant technologies. Responsibilities include developing, implementing, and maintaining methods, operation sequences and processes in the manufacture of fabrication of parts, components, sub-assemblies and final assemblies. Interfaces with product and engineering in coordinating the release of new products. Estimates manufacturing costs, determines time standards, and makes recommendations for tooling an process requirements of new or existing product lines. Maintains records and reporting systems for coordination of manufacturing operations. Typically, a bachelor’s degree in manufacturing or industrial engineering with 2-5 years related work experience or equivalent. Employees with this job title take on progressively more responsibilities demonstrating their knowledge by solving problems of moderate scope with more general direction or oversite. Skilled employees at this level would be expected to manaage smaller projects on their own. Experience working in FDA (Good Manufacturing Practices) and ISO 13485 regulated industry. Immediate need for a Senior Manufacturing Engineer – in Carlsbad, CA who possess: Experience with validating machinery processes Advanced knowledge of equipment validations (IQ/OQ/PQ) Must have strong computer skills Strong sense of customer service and team-oriented skills Excekkent organizational, prioritization and multi-tasking skills Excellent communication skills Strong attention ot detail Professional phone and email etiquette Ability to work independently Essential Functions: design and developing manufacturing procedures, work instructions, tooling, and fixtures that promote product/quality, process efficiency, and operator safety Implement process improvements, troubleshoot equipment, and addressing operator inquiries Generate and modify manufacturing documentation assuring manufacturing process, related documentation, follow established policies and procedures. Utilize LEAN, Six Sigma, and other best practice tools for problem solving and continuous improvement. Assist in identifying equipment needs on the production floor. Generate and modify fixture and tooling drawings using Solid Works Develop and release new products as per internal specifications Write and execute process and equipment validations (IQ/OQ/PQ) Work with external vendors as needed Other assignments as requested For immediate considerations please email your resume to firstname.lastname@example.org
- Quality Assurance Specialist (Vista, CA)on January 14, 2021 at 4:52 pm
Opening for an Quality Assurance Specialist (Vista, CA) SNAPSHOT! Looking to join a pioneering biomedical compant that works with leading research institutes and universities to develope breakthrough technologies? READ ON!! Our client is seeking an experienced and motivated Quality Assurance Specialist with a strong background in medical device manufacturing. The successful candidate will report to the Sr. Director Program Management, Quality Systems and Compliance and work with the team to maintain and manage the quality management system. Knowledge of cGMP, GLP, ISO regulations are a plus. Immediate Opening for Quality Assurance Specialist in Vista, CA who possesses: BS in engineering, technical, or science field 3+ years of work experience in medical device or biotech manufacturing with good understanding of current Good Manufacturing Practices Knowledge of ISO 13485, 21CFR820 1+ years supporting ECO’s, NCR’s, CAPA’s 1+ years supporting audits 2+ years in Document Control MS Word and Excel – basic to intermediate skills Be an independent, self-starter with exceptional communication (written and verbal) skills, detail oriented, organized, and able to prioritize and balance department workloads in a fast-paced environment Demonstrated evidence of a solid background of technical knowledge and experience combined with the proven ability to successfully direct projects and influence people at all organizational levels Must be available to work hours outside of normal workday as needed Experience with electronic quality management systems software a plus Key Responsibilities include: Support Quality System processes in compliance with ISO 13485, 21CFR 820, applicable regulatory requirements and Quality Policy Support Gowning area environment monitoring Support supplier qualification, and supplier corrective actions (SCAR) processes Assign and manage CAPA’s Assist in Complaint handling, NCR’s, and CAPAs/ SCARs Assist in audits and publish audit reports (Internal and External) Assist QA management with special projects Process trending (CAPAs, SCARs, Complaints) Provide support to maintain Quality Management System in accordance with US FDA Quality System Regulations and ISO 13485 for controlled documents (paper and electronic) Reviews incoming documents for completeness and determines proper filing category for accurate archival, retrieval and record keeping Oversee the scanning and upload of documents to the document management system Take charge of all document identification, classification, and filing Assist internal audits and regulatory inspections through retrieval and coordination of documents Routing ECOs, NCRs, CAPAs and various other documents either paper or electronically Maintaining correct revision level of documents in control books (paper and electronically) Check and edit incoming documents and prepare for distribution Support the training program and provide trainings on eQMS and Quality Management System to employees Update and maintain Quality Databases Support other QA/QC functions such as inspection and testing, nonconforming material processing, etc Assist QA management with special projects and other duties as assigned Works collaboratively with the team For immediate consideration, please send your resume to email@example.com!
- Technical Support Engineeron January 12, 2021 at 8:53 pm
Opening for a Technical Support Engineer (Chino, CA) SNAPSHOT! Looking to join a team of leading innovators of visual display solutions offering an extensive line of projectors, monitors, and digital displays for home, corporate, education, government, house of worship, gaming, and digital signage applications! READ ON!! With a long list of award-winning monitors, our client’s displays provide a unique value proposition of forward-thinking performance and avant-garde design. Whether it’s all-white Mac-compatible monitors or displays designed for the demands of 3D printing and CAD/CAM design, our clients monitors bring the industry’s most desired functionalities to professionals and hobbyists alike. Immediate Opening for Technical Support Engineer in Chino, CA who possesses: Technical background and able to learn new technologies quickly Able to communicate & present technical topics/details with clarity to customers, peers, and management Skills in all or most of the following areas: projection, computing, audio/video systems, networking, PC, MAC, Chromebook, software, firmware, system interconnect, electrical wiring, MS Office, and Mobile devices Organized and able to process multiple demands on time in an orderly fashion Process oriented Able to develop plans and processes relevant to role and team operations and then execute Able to calmly guide upset customers to win-win resolutions when faced with technical problems Excellent telephone communication skills Key Responsibilities include: Tech Support in Call Center on DLP Pro-AV & Education Projectors, Professional Monitors, and PDP (Public Display Panels) / IFP’s (Interactive Flat Panels) / Digital Signage Level 1 and Level 2 support for customers • Level 3 support and solution coordination with BenQ headquarter Troubleshoot / Test products to verify operation and accuracy of specs, firmware, and software Generate Return Merchandise Authorizations as appropriate to in-house or 3rd party provider Coordinate with 3rd party on-site providers for on-site service Deploy new products in office to gain hands-on experience and offer training on product operation and feature details for other teams Communicate product issues/solutions to product departments in Texas, California, or Taiwan as appropriate Develop Tech FAQ’s, Case Solutions, and blog posts pro-actively based on product experience and to answer recurring question reducing inbound case load Key role, largely responsible for driving and maintaining Net Promoter Score (NPS) and other Performance Metrix Provide weekly/monthly reporting on top issues & solutions Business travel is required for on-site service or meetings For immediate consideration, please send your resume to firstname.lastname@example.org!
- Quality Manager (Hon January 12, 2021 at 3:47 am
Quality Manager (Hagerstown, MD) SNAPSHOT! Looking to join a growing organization that is acquiring companies and in need of future leaders? READ ON!! This position is responsible for leading the plant Quality Assurance, Quality Control and Quality Engineering systems. This includes all traditional quality verification activities including receiving, in-process inspection, final inspection and testing, audit, and repair activities; continuous improvement (related to Quality); product launch; supplier quality; quality systems compliance; focal point for addressing quality issues with customers, manage customer audits and customer source inspections; safety and environmental compliance of all processes, in particular chemical surface treatment (plating) of metal parts. Our Quality Managers plan, coordinate, and direct the facility quality assurance and control program, the design of which ensures continuous production of products consistent with established standards by performing the following duties personally or through subordinates. Acts as focal for interplant communication and plan development, ensuring a cohesive approach to meeting its and its customers’ quality system requirements. Immediate opening for a Quality Manager in Hagerstown, MD who possesses: Bachelor’s degree with major course work in quality and/or manufacturing engineering is required. Experience as a Quality Assurance Manager in the metal manufacturing industry Experience in recognized quality (ISO9001/AS9100) and process (NADCAP) systems in a metal manufacturing, aerospace, and/or defense environment experience implementing ISO 9001/AS9100 and other quality initiatives Working knowledge of mechanical inspection methods and tools including the ability to read and understand manufacturing routers, instructions, and drawings including GD&T Experience with training and building strong work teams that require minimal management oversight using good delegation skills and understand participative decision-making. Experience overseeing and managing all aspects of quality control and quality assurance in a metal manufacturing, aerospace, or defense environment. ISO 9001 and 9100 experience. Experience with documentation, for example, d250 form familiarity with submitting this type of form. Environmental documentation experience with regards to plating in a highly regulated environment. Experience with very tight tolerances from the military, defense, or aerospace industry Experience working with military customers, such us Northrop, Raytheon, LMCO, DRS, etc, to ensure our products meet their requirements. Requires knowledge in CNC Machining, Sheet Metal Fabrication, Welding, metal chemical surface treatments, assembly and tooling. Strong knowledge and demonstrated experience of Continuous Improvement Practices, Lean Manufacturing and Six Sigma. Strong presentation and training skills required. Strong listening and conflict resolution skills required. Ability to organize and prioritize work. Must have the ability to make recommendations to effectively resolve problems or issues, by using judgment that is consistent with company standards, practices, policies, procedures, including disciplinary issues, regulations and/or labor law. Ability to work well with others and in a team environment. Key Responsibilities include: Hands-on experience on the manufacturing floor with a focus on driving quality improvements. Ensure that processes needed for the Quality Management System (QMS) are established, implemented, and maintained. Ensure the promotion of awareness of customer requirements throughout the organization. Develop, collect, and report performance metrics as needed to senior management including defect and scrap data including corrective action status. Provides budgetary inputs for training and ongoing quality assurance activities to meet near and long-term contract requirements. Establishing systems for data collection and analysis and using that data to drive continuous improvement activities. Plan, lead and measure process and voice of customer performance and quality system effectiveness and adjust in strategy and/or procedures as necessary. Lead proactive quality improvements through the proper execution of Advanced Product Quality Planning (APQP) within the facility to ensure the flawless launch of new products and managing quality deliverables associated with product and process design changes. Through familiarity with customer requirements, analyzes existing quality procedures and systems to determine their level of compliance to requirements. Oversees inspections of materials, materials in process, and finished products. Responsible for the development of quality standards and protocols for quality assurance testing models. Formulates quality control objectives for the facility, e.g. defect reduction and operator certification for specified quality tasks and coordinates the objectives with production management and manufacturing procedures to maximize product reliability and minimize costs associated with rework, scrap, and escapements. Works to develop and facilitate a cohesive team environment which builds confidence and strong morale among inspection personnel and between inspection and manufacturing and support personnel. Ensure that all new staff is inducted into the requirements of the QMS related to their own roles and responsibilities. Provide update training as necessary. Investigates and responds to customer complaints regarding quality. This may entail technical responses to written claims and complaints, on-site visits to customer facilities, negotiation with customer quality representatives and/or reporting process capability, and out-of-scope issues to interested customer service and program management personnel. Develops a cooperative, professional relationship with manufacturing management in order to facilitate and coordinate functions and operations between the departments and to establish responsibilities, procedures, and criteria for attaining quality and manufacturing objectives. Evaluates constraints of the existing quality department processes and procedures and develops strategies to address and resolve the constraints (e.g. source backlog, variability in inspection criteria/interpretation, random auditing, sampling) and monitors backlog of future work in order to adjust staffing requirements by moving existing personnel or adding personnel as appropriate. Ensure that document control procedure is utilized to approve, review, and update all changes to critical documents within the scope of the QMS. Manage, coach, and develop the quality team and promote a positive quality culture throughout the facility by establishing sound systems and a demonstrated process focus. Carries out personnel management responsibilities in accordance with the organization’s policies and applicable laws. Responsibilities include interviewing, hiring, and training employees; planning, assigning and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems. Monitors the safety and compliance of processes, in particular the chemical surface treatment (plating, passivation, etc) in order to control the mix of chemicals to meet the requirements and manage hazardous waste meeting requirements Responsible for leading and driving activities to achieve quality improvements in the operations of the plant, that lead to positive performance and financial impacts. Manage and develop Key Performance Indicators that drive the improvement activities and create daily accountability. Report on daily performance selected KPIs. Apply statistical methods and perform product/process analysis for cost reduction, quality improvement, and improved efficiency. Employ Lean Six Sigma methodologies and tools in order to accomplish business objectives Perform other related duties as assigned. For immediate consideration, please send your resume to email@example.com!
https://snapstaffing.com/wp-content/uploads/2019/03/snap-logo-web.png 0 0 Jason Card https://snapstaffing.com/wp-content/uploads/2019/03/snap-logo-web.png Jason Card2019-03-17 20:30:452019-03-17 20:33:15