Quality Engineer Jobs in Irvine, CA

Pride Health is hiring a Program Manager for Quality Improvement for one of its clients in California. This is a 3-month contract with the possibility of a Contract to Hire with competitive pay and benefits. Pay range - $60 - $70 per hour on W2 (Based on relevant experience) Length of assignment - 3 months contract (Possibility of Contract to Hire) Shift - M-F 8 am-4:30 pm; 100% onsite. Job Summary Responsible for establishing and continuing effective quality improvement efforts to achieve organizational performance goals and national top decile performance in clinical excellence. Quality improvements may be small or large scale and are in alignment with Hoag's strategic goals for example, addressing 30-day readmissions and mortality reduction. The Quality Improvement Manager may apply Lean, Six Sigma, and other quality improvement methodologies to deliver results. Roles are very specific - candidates must have in-depth experience in Clinical Quality Improvement in a hospital inpatient setting. Job Duties Coaches and trains teams in the utilization of improvement tools and implementation of improvements. Manage plans and develop guidelines, process measures, targets, and standards for monitoring and measuring results to deliver on goals. Interacts daily with leaders, to identify, define, and manage opportunities to improve quality while helping create a strategic approach to produce and establish extraordinary improvement. The Program Manager Quality Improvement collaborates to lead and organize efforts for continuous clinical improvement. Requirements Required Education: Bachelor's degree in Industrial Engineering, Business/Healthcare Administration, Life Sciences or equivalent Medical Foundation, Physician Practice, or Health Plan related experience Preferred Education: Master's degree in Industrial Engineering, Business/Healthcare Administration, or Public Health Consulting experience Master's degree in Healthcare Administration or Public Health. Preferred Certifications & Licensure: Certifications in Lean and/or Six Sigma Methodology Project Management Professional (PMP) certification Required Skills & Experience: Five years' experience in performance/process improvement projects including but not limited to Lean, and Six Sigma methodologies. Advanced training or experience in performing statistical, financial, and strategic analysis Demonstrated performance improvement and process improvement skills and knowledge of methodologies such as Lean, Six Sigma, DMAIC, and PDCA Highly proficient in Microsoft Project and the Microsoft Office Suite (Word, Excel, PowerPoint, Visio) Comprehensive digital marketing skills Candidates must possess all 4 of the below: Completed PI training and certification (Six Sigma, lean, CPHQ, Masters in Improvement) from nationally recognized organizations (e.g., ASQ). Current or past formal position in Quality Improvement/Performance Improvement (minimum 2 years) History of leading and improving quality outcome metrics such as readmissions, mortality, hospital-acquired conditions (infections, falls, pressure injuries, medication errors), sepsis care, venous thromboembolism, unplanned extubations, delirium, complications, c-section, exclusive breastfeeding, etc). Experience using key driver diagrams, Pareto charts, excel pivot tables, and project management tools. Benefits Pride Global offers eligible employees comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance, and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance, and employee discounts with preferred vendors. Equal Opportunity Employer As a certified minority-owned business, Pride Global and its affiliates - including Russell Tobin, Pride Health, and Pride Now - are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, pregnancy, disability, age, veteran status, or other characteristics.

This position will be an integral part of our organization that is responsible for the development of medical technology and innovative, world-class products that save people's lives. The Quality Manager is responsible for leading the corporate product quality systems, including setting corporate quality goals, managing and improving all aspects of the quality system, product quality, and documentation requirements for advanced electronic medical devices. Duties & Responsibilities: Defines, develops, and implements quality system procedures, work instructions, and forms. Must work with limited supervision and will be involved in and have input to project planning. Proficient in clearly communicating directions and in influencing people in adopting the best solutions, tools, working practices and promotes cooperation in defining an excellent technical product. Initiates and performs internal and supplier audits Works in collaboration with R&D Engineers and executes the quality tasks of the NPD (New product Development) process, such as Verification and Validation of new products, Risk Management, and Quality Control. Works with Engineering and Manufacturing regarding product and process improvements Initiates and participates in Continuous Improvement projects. Coordinates the quality aspect of Customer Complaints and CAPA processes. Minimum Qualifications and Experience: BS in Mechanical or Electrical Engineering with minimum of 5 years of working experience, as a Quality Engineer, in a medical device manufacturing environment is a must. Excellent conceptual, analytical, and problem-solving ability. Good communication skills, both verbal and written, and the ability to interface effectively with engineering and manufacturing personnel. Working experience with ISO 13486 is a must. Working experience with investigation tools such as Fishbone diagram, Brainstorming, and Pareto charts is a must. Quality Engineer and Quality Auditor certifications (CQE, CQA) are a plus. Working experience with Minitab or any other data analysis software is a big plus. Use of ERP systems to support the quality system and quality initiatives. Proven competencies in: Analysis and reporting Communication and presentation Customer focus Change champion MS Office suite (Office, Word, Excel, PowerPoint) Preferred Qualifications: Experience working in both large structured and small entrepreneurial organizations. Physical requirements/Work Environment: This position is located in Irvine, CA. This position primarily works in an office environment. It requires frequent sitting, standing and walking. Daily use of a computer and other computing and digital devices is required. May stand for extended periods when facilitating meetings or walking in the facilities. Some local travel is necessary so the ability to operate a motor vehicle and maintain a valid driver's license is required. The physical demands of the position described herein are essential functions of the job and employees must be able to successfully perform these tasks for extended periods. Reasonable accommodations may be made for those individuals with real or perceived disabilities to perform the essential functions of the job described.

The Quality Technician - NDT uses inspection skills in Eddy Current (ET), Magnetic Particle (MT) and Liquid Dye Penetrant (PT) methods to verify that Attractions and Attraction components meet applicable requirements. Responsibilities include interpreting drawings, schematics and other relevant documents to determine and use the correct MT and PT instruments and materials to check for structural integrity! This position is also responsible to preparing material surfaces by wire brushing, sand blasting, bead blasting, stripping, or other means as necessary to prepare the surface for inspection. The use of hand tools for metal removal as the need arises. Quality Technicians record and document the results of inspections for transmittal to the appropriate engineering function. Basic Qualifications : You must be at least 18 years of age to be considered for this role Disney Behaviors: Upbeat and able to work in a fast paced environment, physical stamina, respect for diversity, committed and reliable- reports to assignments on time, with required tools and materials, and prepared for work. Develop and appreciate for the Disney Five Keys: Safety, Courtesy, Show, Efficiency and Inclusion Service Orientation: Hardworking and eager to accept new challenges. Receptive to special requests and special assignments, able to work in a fast paced environment, often stressful, Team Environment Team Behaviors: Good interpersonal skills- ability to relate to fellow Cast Members, management, vendors, and other Cast Members from Disney divisions outside of the resort. Spirit of collaboration. Detail Orientation: Can complete repetitious tasks while maintaining quality, Can problem tackle and build appropriate solutions. Prior Level II certification in MT and PT and have worked in this capacity within the last six (6) months Individuals in this position must pass a general, specific, and practical exam in accordance with national nondestructive testing standards. Schedule Availability - Must be open to any shift (1st, 2nd, and 3rd shift) including holidays, with any combination of days off. Additional Information : SCHEDULE AVAILABILITY Our Theme Parks and Resort Hotels operate 24 hours a day, 365 days a year and some shifts may start as early as 5:00am while some may end as late as 3:00am, 4:00am or 5:00am. Please note that the principles of seniority are used to schedule all roles. SUBMITTING YOUR APPLICATION After clicking “Apply Now” below, the employment application will open in a new window. Please complete ALL pages of the application by clicking “Next” on each page, then “Submit” on the final page. KEYWORD: dlrcasting, dlr casting, Disneyland Resort Casting Hourly Jobs , DLRResortRoles, DLR Resort Roles, Facilities, HeroesWorkHere The pay rate for this role in California is $46.40 to $52.00 per hour, which follows the pay scale agreed upon in the Collective Bargaining Agreement. The base pay actually offered may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience, among other factors. Select benefits may be provided as part of the compensation package, such as medical, financial, and/or other benefits. To learn more about our benefits visit: ****************************************

Seeking a Quality Engineer to test and improve product design, functionality, and compliance with quality standards. Responsibilities: Develops sampling procedures and quality evaluation methods. Ensures precision and accuracy of production and testing equipment. May create training materials and conduct quality control training. May specialize in design, process control, product evaluation, reliability, or software quality. Skills: Strong analytical, problem-solving, and communication skills. Ability to read blueprints and technical drawings. Experience with CAD and engineering software. Requirements: Bachelor's degree in Engineering. 2-4 years of relevant experience.

Join Yorke Engineering, LLC, an Environmental Consulting leader in California that implements Environmental Engineering and Compliance solutions for our clients throughout California. Our mission is to solve environmental compliance problems for industrial and governmental/infrastructure facilities. We are a growing and dynamic organization of highly respected professionals. Yorke Engineering, LLC has assisted over 1,400 client organizations with their Air Quality and Environmental Compliance, Engineering, and Permitting needs. Our philosophy is to efficiently help government and industrial customers with the complex array of environmental laws and regulations. From simple permits to complex agency negotiations, from small companies to the largest of California's organizations, Yorke successfully solves our clients' Air Quality and Environmental challenges. Our team has over 1,000 years of combined environmental experience and consists of engineers and scientists that specialize in Air Quality, Waste, Water, CEQA, Safety, and Industrial Hygiene. We are looking for a sharp Air Quality Engineer / Scientist (Environmental Permitting and Compliance Specialist) to join our team in any of our Southern CA offices (Diamond Bar, Long Beach, Los Angeles, San Juan Capistrano, San Diego, Ventura, or Riverside) during our normal business hours. We offer competitive salaries, a full benefits package including Paid Time Off, Holidays, Full Medical/Dental/Vision, along with a 401k program with a generous company match. Position Summary: The Air Quality Engineer / Scientist (Environmental Permitting and Compliance Specialist) performs professional engineering work, executing the compliance and permitting functions in relation to Air Quality Regulations and Compliance. This candidate will be reviewing processes and equipment, analyzing permit-related technical and regulatory issues, and communicating those analyses within Yorke, the client organization, with government agencies and with the public at large. The work is challenging, broad in scope, and variable from project to project. The position involves effective communication, decision-making, and time management. The candidate performs other duties as required or assigned. The candidate qualifications we are seeking include: 5-15 years of work experience in the Air Quality and/or Environmental industry in an engineering role (preferably in a consulting environment); Experience as an active team member in the environmental services industry as a consultant focusing on: Process and equipment review; Air quality permitting under SCAQMD, and other Air Districts, including Title V permitting; RECLAIM implementation and reporting; Annual Emissions Reporting; Air Dispersion Modeling; Air Quality Assessments including Data Analysis and Emission Inventories; General Air Quality Compliance for facilities in CA, including problem solving. Ability to be an active team member on project teams towards project completion within project scope, budget and schedule and ensure quality work product and deliverables; Ability to work with clients, staff, and regulators through effective communication and expertise by fostering a collaborative environment without losing focus of quality; Proven track record or desire to engage in successful regulatory work in dealing with the SCAQMD, EPA, CARB and/or other similar regulatory agencies; Experience or desire to work on-site at client facilities; Prepare reports and submissions in timely manner; Experience with handling highly technical data and technical data interpretation; Highly motivated to continue working in Air Quality environmental field and expand their knowledge and experience; CA Regulatory/Compliance experience is required. Job Requirements: B.S or M.S. degree in Chemical Engineering, Environmental Engineering, or Mechanical Engineering, or other relevant technical degrees from an accredited college (minimum GPA of 3.0); Ability to work collaboratively in a team fashion, handle several projects at once, prioritize work, and work efficiently; Desire to learn or developing technical expertise in environmental rules and regulations; Excellent oral and written communications skills; Experience in conflict resolution and crisis management; Track record of successful analysis, interpretation, and application of rules and regulations towards practical solutions; Ability to think critically and develop solutions; Software Knowledge: Strong Microsoft Excel, Word, Outlook, and Powerpoint skills (required); Microsoft 365 Applications, including Sharepoint (a plus) EIT, CPP or P.E. (a plus).

Kelly Science, Engineering, Technology, and Telecom, a managed solution provider and business unit of Kelly Services, is seeking Design Quality Engineers for a long-term contract with one of our global medical device clients in Irvine, CA. Our Client is a global leader in the science of diagnosing and treating heart rhythm disorders. Established their leadership in electrophysiology with the development of the first real-time, 3D cardiac mapping and navigation technology, as well as the first electrophysiology catheter. Join a Leading Innovator in Cardiac Care and Device Developmen t The Design Quality Engineers will be supporting the transfer between NPD and Manufacturing. HYBRID 2 days on-site one week, 3 days on-site the next…there will be times when they need to be on site 5 days when there is testin g. Key Responsibiliti es:• Utilizing Quality Engineering tools/processes in the development and implementation of practices for the effective and efficient development, transfer, and maintenance of products/processes throughout the product lifecyc le.• Leading efforts for continuous quality and customer satisfaction improvement opportuniti es.• Support the Non-Conformance Report (NCR) process for facilities located in the U .S.• Develop and establish effective quality control and support associated risk management plans, AFMEA, DFMEA and PFM EA.• Write, review and/or approve process and product validation protocols and reports, equipment qualifications, and engineering change orde rs.• Use statistical tools to analyze data, make acceptance decisions, and improve process capability (Six Sigma, Statistical Process Control (S PC)• Design of Experiments (DOE), e tc.• Ensure that development activities follow design control requirements (Design Trace Matrix), product is tested per applicable standards, GSPR is met per the MDR, and product is properly transferred to manufacturing per applicable specificatio ns.• Technical problem-solving, failure analysis, and root cause determinati on.• Makes decisions independently on engineering problems and methods and represents the organization in conferences to resolve important questions and to plan and coordinate wo rk.• Assesses the feasibility and soundness of proposed engineering evaluation tests, products or equipme nt.• Assigns/reviews quality inspection testing and test da ta.• Keeps department supervisor abreast of activities and issues of the quality gro up.• Responsible for ensuring personal and Company complia nce• Performs other duties assigned as nee ded REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICE NSES• Bachelor's degree, required; preferably in engineering and/or scientific discip line• 4-5 years of design quality engineering experie nce.• Catheter experience or class 3 delivery prefe rred• Experience in design transfer - DBT (testing of finished devi ces)• Process/equipment investigat ions• CAPA experience a plus• Manufacturing, or research and development experience in medical dev ices• Ability to define problems, collect and analyze data, establish f acts• Ability to develop and implement Quality stand ards• Demonstrated auditing and problem-solving sk ills• Knowledge of leading-edge Quality Engineering, design control, and (V&V) t ools• Ability to effectively collaborate and communicate with internal and external part ners• Theoretical and practical fundamentals such as DOE, DMAIC and ANOVA is a p lus.• Knowledge of SolidWorks, and CAD-based prog rams• Six Sigma/ Design for Six Sigma experience, and/or knowledge of Process Excell ence• Knowledge of Quality and operations systems and processes, including GMP is a p lus. Important information: This position is recruited for by a remote Kelly office, not your local Kelly branch. Applicants must be legally permitted to work in the United States immediately and without employer spo nsors

INTRODUCTION Barksdale, founded in 1949, is a leading manufacturer of highly engineered control products. As a subsidiary of Crane Co. a $2B industrial conglomerate, Barksdale has a leading brand position in instrumentation, with focus on General Industrial, Oil & Gas and Transportation end markets. With proprietary technologies, Barksdale's, regulators, pressure switches and electronic instrumentation products have carved a niche for themselves in demanding applications. SUMMARY The Quality Engineer is expected to establish, maintain and improve all responsible areas of the Quality System to ensure manufacturing processes are controlled and pertinent processes are regularly reviewed, analyzed and reported in an effort to support continuous improvement within the manufacturing facility. The scope of this role shall include, but not be limited to the development and operation of quality control systems, application and analysis of testing and inspection procedures, the ability to use metrology and advanced statistical methods to diagnose and correct improper quality control practices, an understanding of human factors and motivation, facilitate the adoption of quality concepts and techniques, and posses the knowledge and ability to develop and administer management information systems and to audit quality systems for deficiency identification and correction. SPECIFIC DUTIES AND RESPONSIBILITIES Primary Develop and implement quality programs, including tracking, analyzing, reporting, and problem solving. Maintain, improve, and enforce Quality Management System (QMS) in accordance to all internal, external (ISO 9001, IATF 16949, ISO/IEC 80079-34, and ATEX Directive), and customer specific requirements. Execute Core Tools (DFMEA, PFMEA, MSA, SPC, and PPAP). Work with cross functional team and apply problem solving tools (i.e. 5-Whys, Fishbone, DMAIC, etc.) as part of root cause analysis and identify corrective actions. Acquire, analyze, and present data using appropriate standard quantitative methods across a spectrum of business environments to facilitate process analysis and improvements. Manage the Corrective Action Program (CAPA), including the assurance that issues are addressed in a timely manner and that corrective actions are effective. Assist in quality issues from suppliers, production, and/or customers, including any communications with them. Collaborate in PPAP submissions (for both suppliers and customers), including the review and final approval of the Part Submission Warranty (PSW). Provide assistance and coaching to peers and suppliers in order to resolve quality conflicts, continually improve quality, reduce cost, etc. Plan, control, and assure product and process quality in accordance with quality principles, which includes planning processes, material control, acceptance sampling, and measurement systems. Conduct hands-on product evaluations for any type of customer return/complaint. Secondary Participate in New Product Development (APQP) projects. Production introduction shall be accompanied by Quality validation using DVP&R and advanced statistical methods (i.e. Gage R&R, Capability Studies, etc.). Participate in various Kaizen events and projects in order to drive continuous improvement. Review PCRs/PCOs (ECRs/ECOs). Chair MRB for swift, accurate disposition of nonconforming material. Monitor and review Cost of Poor Quality (COPQ). Complete IMDS reports per PPAP requirements. Perform and/or facilitate 1st, 2nd, and 3rd party audits in the ISO 9001, IATF16949, ISO/IEC 80079-34, VDA, CQI, and ATEX Directive environments. Participate in the Internal Audit program. PROFESSIONAL EXPERIENCE/ QUALIFICATIONS BS degree in Technical discipline with a minimum of 3 years of experience in Quality. Industrial Engineering or similar preferred. Industry certification (i.e. ASQ Certified Quality Engineer) preferred. Some formal Six Sigma training preferred. Must have experience with electronics. Must posses basic to intermediate level of understanding in quality philosophies, principles, systems, methods, tools, standards, organizational and team dynamics, customer expectations and satisfaction, supplier relations and performance, leadership, training, interpersonal relationships, improvement systems, and professional ethics. Must have basic understanding of quality management systems and its development, documentation, and implementation with respect to domestic and international regulatory standards or requirements. Must have basic to intermediate knowledge of quality concepts and methods such as FMEA, SPC, MSA, Lean Manufacturing, CAPA, Six Sigma, 5S, etc. Must have intermediate knowledge of basic statistical concepts (FPY, rate, %, average, std deviation, etc.). Must be able to make decisions using risk-based thinking and data driven analytical thinking. Must have strong knowledge of GD&T. Strong teamwork with outward attitude of support towards members of the department and the company. Strong communication skills (both oral and written). Strong ability to organize team with ability to assemble, coordinate, schedule, and execute interdepartmental activities. Strong time management skills with ability to prioritize effectively based on business needs. Able to interpret engineering drawings, test procedures, work orders, BOMs, written procedures, international standards, etc. Must be able to analyze, interpret, and report on data in Microsoft Excel. Must be comfortable with hands-on work. Must be able to stand and move parts physically. Must be flexible to travel (both domestically and internationally) and work overtime as required. SKILLS Microsoft Word, Excel, PowerPoint, Outlook Windows File Structure ERP System (QAD) Customer Portals (web-based) Minitab Salary range: $73,200 to $89,200 with 5% bonus potential. Several factors contribute to actual salary, including experience in a similar role or performing comparable job responsibilities, skills, training, and other qualifications. Compensation packages also include comprehensive benefits, 401K contribution and match, Paid Time Off, paid holidays, tuition reimbursement and more. Some roles may be eligible for participation in performance-based bonus programs

Job Title: Quality Engineer (Automotive Industry) Shift: Monday - Friday, 6:00 am - 2:30 pm Pay: $75,000 - $115,000 The Quality Engineer ensures compliance with ISO 9001 in a metal stamping/Automotive plant, improving quality processes and maintaining customer requirements. Responsibilities include developing and implementing quality assurance procedures, training employees, overseeing returned materials, and supporting supplier development. Key Responsibilities: Prepare and review AIAG PPAP submissions. Develop and implement inspection, testing, and evaluation methods. Support ISO 9001 certification and transition to IATF 16949. Conduct internal audits and assist in corrective actions. Train employees on quality procedures and self-inspection. Maintain process documentation (Flow Diagrams, PFMEA, Control Plans). Interface with internal teams, customers, and suppliers to ensure quality compliance. Qualifications & Technical Skills Required: Years/Type of Exp: 10 years preferred - Automotive Manufacturing Experience required Education: 5+ years' experience in manufacturing or bachelor's degree (B.S.) in mechanical engineering or industrial engineering or equivalent related work experience preferred. Must be able to read and interpret blueprints, tool designs, and other technical drawings. Formal SPC, ISO-9001 - IATF 16949, ASME Y145, drawing standards and evaluation, QA systems analysis and documentation implementation. Computer literate in Microsoft Office/Outlook. Hardware: Computers: Must be computer literate. Must have experience using inspection equipment. Systems & Software: All phases of ISO 9001 & IATF 16949 Required Software. PPAP and ISO Forms Specialized Training/Knowledge: Knowledge of creating Process Flow Diagram, PFMEA and Control Plan. AIAG PPAP experience - AIAG Core Tools Root cause analysis experience/techniques required #QualityEngineer #AutomotiveIndustry #ISO9001 #IATF16949 #ManufacturingJobs #EngineeringJobs #ChinoCAJobs #AutomotiveCareers #QualityAssurance #EngineeringOpportunities #JobOpening #HiringNow #CareerOpportunity #JobSearch

The Quality Engineer (QE) supports production by ensuring products and processes meet our quality standards. This role involves monitoring production, identifying defects, implementing corrective actions, and working with Planning to validate operations in routing documents and the ERP system. Key Responsibilities: Establish and refine quality standards to prevent defects in components and final products. Collaborate cross-functionally to identify and mitigate quality risks. Review and approve protocols, reports, and specifications. Audit production, raw materials, and suppliers to ensure compliance. Conduct root cause analysis for defects and non-conformities. Perform process impact and product risk assessments. Ensure compliance with external quality standards (e.g., ISO 9001). Skills & Expertise: Strong knowledge of business practices and quality principles. Works independently with sound judgment to resolve complex issues. Experience with quality control innovation and technical analysis. Effective communication with internal teams and external vendors. Requirements: Bachelor's degree or 6-8 years of related experience preferred. Onsite role (no hybrid/remote, except as approved by QA Manager). Availability Monday-Friday, with overtime as required.

Duration - 1 Year, Contract, W-2 Pay - $35- $41.03 an hour * Responsible for supplier quality audits, vendor management, and maintaining supplier quality metrics. * Provide receiving inspection floor support, perform test method development, run supplier meetings, and design/risk document creation. * Work in close partnership with Quality, R&D, Operations, Sourcing, and RA. * Audit, monitor, evaluate, report and improve supplier quality system performance and provide technical support to suppliers * Perform supplier evaluations including on-site audits to assess supplier capabilities, determine approval status, and verify corrective action * Collect and add supplier information required for the Approved Supplier List * Conduct component and product quality testing for purposes of supplier and component qualification and improvement * Identify and implement statistical engineering tools and techniques to evaluate supplier process capability and technical performance * Evaluate supplier quality systems, strategies, and regulatory compliance via vendor audits * Collect and analyze quality metrics relating to Supplier Quality * Identify and define correction actions and follow-up to ensure completeness and effectiveness * Communicate supplier quality risks to upper management while suggesting improvements and cost savings where possible Qualifications: * Bachelor's degree in Engineering or Scientific field & Medical device, pharma, or biotech industry experience * Experience with supplier quality engineering activities including external supplier vendor audits for class II and class III medical devices * Previous experience in design/prototyping using Solidworks/Creo (CAD software) drafting experience required * Statistical analysis (Minitab), Excel macro coding, Power BI skills highly preferred * Effective problem-solving techniques (i.e. Root Cause Analysis, FMEA process, Gage R&R, Validation activities, etc.) * Conduct effective root cause investigations; assessment of corrective action strategies; and effectiveness as applied to NCRs and SCARs * Demonstrated ability to apply statistical quality engineering tools in a supplier environment * Working knowledge of International and Domestic FDA regulations * Thorough understanding of Risk Management principles * Strong communication and organizational skills to effectively manage and get results with external suppliers * Six Sigma Black Belt/LEAN Manufacturing experience * ASQ Certified Quality Engineer or ASQ/BSI Certified Quality Auditor All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

Evaluate quality processes, procedures, and statistical techniques; analyze production and service limitations and standards; recommend revisions to specifications. Assist in formulating quality policies and procedures, collaborating with engineering departments, customers, and suppliers on quality issues. Ensure quality standards are met for specific customers, programs, and projects, including reviewing customer quotes, contracts, and ensuring acceptable product shipments. Essential Duties and Responsibilities: Prepare, review, and approve quality plans and specifications, recommending process improvements. Review material certifications, work orders, test reports, and inspection data for accuracy. Collaborate daily with internal engineering teams, resolving product quality issues. Ensure customer quality requirements are conveyed to suppliers and incorporated into manufacturing work instructions. Participate in Material Review Board (MRB) and continuous improvement projects. Conduct failure investigations, corrective actions, and customer complaint resolutions. Review and approve drawings per GD&T standards. Liaise between design engineering, manufacturing, and other departments to ensure product conformance. Coordinate customer/government inspections and attend related meetings. Support internal and external audits, documenting results and corrective actions. Qualifications: Experience with government contracts and ISO 9001/AS9100 standards. Knowledge of inspection methods in design and fabrication. Strong communication skills for interacting with internal teams and external customers/suppliers. Proficiency in MS Office (Word, Excel, PowerPoint, Outlook). Ability to read and interpret blueprints and specifications. Education and Experience: Bachelor's degree in Mechanical Engineering or related discipline. 3-6 years of experience in a Quality Assurance department within aerospace manufacturing or equivalent experience.

We are seeking a highly skilled Senior QA Engineer to join our team. Our team focusses on providing a software stack for Design Verification of the PCBAs and ECUs (Electronic Component Units) for current and next-gen vehicle platforms (Autonomy, Infotainment, Vehicle Controls, etc.). You will be responsible for building hardware-in-the-loop (HIL) and regression testing setups using Python, Openhtf, and Pytest. This role requires proficiency in high-level scripting languages and a solid understanding of embedded systems testing methodologies. Key Responsibilities: Design architectures and develop robust and scalable test setups (HIL) for embedded systems validation. Maintain automation, test frameworks, and systems at scale for usage in rapid engineering development. Develop multi-tiered test suites to ensure the detection of regressions. Collaborate with hardware design, firmware, and test engineers to implement embedded solution simulations and address testing gaps. Improve test coverage and reliability by developing new test cases and refining existing ones. Partner with product management and engineering peers to design verifiable end-to-end test cases through automated testing. Required Qualifications: 8+ years of experience in software testing and automation, specifically in embedded systems. Strong expertise in Python scripting, Pytest, and OpenHTF. Proven experience in setting up and executing regression tests in HIL-like environments. Deep understanding of hardware and embedded systems testing methodologies. Experience with hardware interfaces such as UART, I2C, SPI, and CAN. Strong debugging skills with the ability to analyze logs and failure reports. Familiarity with version control systems (Git) and Continuous Integration (CI) systems like GitLab CI. Preferred Qualifications: Experience working with embedded systems. Knowledge of Docker and virtualization for test environments. Hands-on experience with test equipment (oscilloscopes, logic analyzers, power supplies). Background in automotive, aerospace, or IoT industries. Experience with NI VeriStand, Vector CANoe, and Wireshark for testing and validation.

As an Insulation Line Process Engineer, you will be responsible for developing and standardizing the covered conductor process, setting up the lab, and creating various materials for the insulation process. This role requires a strong understanding of insulation materials, Insulation Line Process Engineering, and laboratory setup. In addition, the position is responsible for correcting and improving manufacturing processes, systems, and operations with the goal of developing more advanced applied engineering skills. The expectations are that you will make valuable contributions to engineering projects, actively participate in project tasks, assist in design, development, testing, and implementation processes, and contribute effectively to project outcomes, meeting deadlines, and achieving project goals. This position will work on R&D, standardization, troubleshooting and resolving technical issues that arise during production and testing, analyzing problems, proposing solutions, and implementing corrective actions. The objective is to develop and standardize the covered conductor process, while implementing continuous improvement and driving toward operational excellence. Essential Functions Foster a zero-injury culture: conduct risk assessments and implement safety protocols to minimize hazards and ensure a safe working environment. Develop and standardize the covered conductor process to ensure consistent quality and efficiency. Set up and maintain the laboratory for insulation process testing and development. Create and test various materials for the insulation process, ensuring they meet industry standards and specifications. Perform materials inspection of raw material, work in process (WIP) and finished goods. Collaborate with cross-functional teams, including R&D, production, and quality assurance, to optimize the insulation process. Conduct research and stay updated on the latest advancements in insulation materials and technologies. Troubleshoot and resolve any issues related to the insulation process and materials. Document and report on process improvements, test results, and material performance. Ensure compliance with safety and environmental regulations in all aspects of the insulation process. Improve productivity by performing ergonomic evaluations, time studies, simulation, and line balancing, including studying and improving plant safety. Perform cost analyses to aid decision-making for proposed processes or projects. Carry out Capacity utilization analyses. Identify critical operating parameters and implement process control strategies to ensure consistency of output while reducing dependence on product testing. Apply work-load models to optimize employee occupation, ensuring efficient and cost-effective production. Take inventory and provide reports as necessary. Create engineering drawings, conduct calculations, and collaborate with cross-functional teams to refine designs. Lead process troubleshooting efforts to identify root causes of production issues and implement corrective actions. Create and manage process documentation including creation of SOPs, technical reports, specifications, and project plans. Maintain accurate records of design and process changes, test results, and project progress. Assist in conducting tests, experiments, simulations and feasibility studies to evaluate the performance and reliability of raw material, product, system, and processes. Assist Quality Control to ensure adherence to engineering standards and specifications. Practice 5 Whys methodology to determine root cause of process issues/failures, and implement actions to prevent reoccurrence. Collaborate with cross-functional teams, including production, engineering and quality assurance to identify process improvement opportunities. Participate in meetings, provide updates on progress, and contribute to effective communication within the team. Participate in the design and commissioning of new production facilities, including equipment selection, installation, and startup activities. Adhere to relevant industry standards, regulations, and safety protocols to ensure that work meets legal and regulatory requirements. Assist in obtaining necessary certifications or approvals. Follow company rules and guidelines. Comply with cross-training and other training requirements. Other duties may be assigned as needed, such as supporting preventative maintenance tasks, spare parts, and tooling management. Requirements / Training and Experience Bachelor's degree in Chemical Engineering, Materials Science, or a related field. One or two years of hands-on experience in a manufacturing company or internship in a related field is highly desired. Proven experience in Insulation Line Process Engineering, preferably in the insulation industry. Strong knowledge of insulation materials and their properties. Experience in laboratory setup and maintenance. Excellent problem-solving and analytical skills. Strong communication and teamwork abilities. Ability to work independently and manage multiple projects simultaneously. Effective verbal and written communication skills with the ability to collaborate effectively with cross-functional teams. Ability to comprehend and follow directions. Basic understanding of ISO-9000 quality management system principles. Adept at multi-tasking: able to manage multiple priorities and deadlines. Strong commitment to safety, quality, and continuous improvement Proficient with Microsoft Office Suite or related software programs. Ability to meet attendance expectations in a fast-paced manufacturing environment. Willingness to work off hours or on off-shifts to meet promised timelines and deliverables. Ability to maintain a professional, positive attitude. Must be able to successfully pass e-Verify background check. Preferred Qualifications: Master's degree in Chemical Engineering, Materials Science, or a related field. Experience with covered conductor processes and materials. Knowledge of industry standards and regulations related to insulation materials. Experience using statistical software packages such as Statistica or MiniTab is preferred. Experience using a database such as FoxPro, Oracle or SQL Server is highly desired. Some experience with CAD tools such as AutoCad or SolidWorks is a plus. Incentives Benefits offered the first of the month following 30 days of employment, include: medical, dental, life insurance, long term disability, paid time off (sick and vacation), 10 company holidays, 401(k) with company match, etc. Referral Rewards program Salary Range: $90,000.00 To $160,000 Annually Work Environment The Insulation Line Process Engineer position works in a combination of work settings from office, lab to a safety sensitive manufacturing environment. The Insulation Line Process Engineer will often work directly on the shop floor of the manufacturing facility, near and around large-scale production processes and equipment. The Insulation Line Process Engineer may also work in Research and Development (R&D) and Quality Control Testing to design and develop new manufacturing processes, testing, and experiments to improve product design and production methods, and to ensure product quality and compliance with standards. The position will spend time in the engineering office performing tasks such as designing manufacturing systems, developing process flow diagrams, analyzing data, creating manufacturing instructions, and collaborating with others. Occasionally, the Insulation Line Process Engineer will participate in on-site visits needed to visit suppliers, vendors, or customer sites to review quality issues, assess manufacturing capabilities, troubleshoot production issues, or assess material or tooling quality and performance. Occupational health and safety practices are essential in manufacturing environments, and the Insulation Line Process Engineer is expected to adhere to safety protocols and wear appropriate protective equipment when necessary.

Process Engineer- TalentZok Are you looking for a new career opportunity with an exciting company?! Then we've got the right team for you! In this role, you're responsible for the duties listed below. Immediate opening for a Process Engineer in Costa Mesa, CA who possesses: 5-7 year's hands-on experience with Plastic Injection Molding Scientific Molding Certification or Degree in Manufacturing or Engineering Experience with ISO 9001/AS9100/ISO 13485 preferred Email resumes to ******************** or call ************. FULL DESCRIPTION : The Process Engineer is a hands-on position that plans, directs, and coordinates manufacturing equipment and processes to produce high-quality injection molded products. This role is responsible for coordinating the molding efforts on new program launches, setting up and/or revising manufacturing processes, and assisting manufacturing operations in problem-solving and continuous process improvements. The Process Engineer shall monitor the effectiveness of production processes, quantify and document findings, and present them to management. This position also mentors and provides training and guidance to other injection molding personnel. The selected candidate will be responsible for: Develop new processes, assess and document new and existing processes. Implement and evaluate changes to improve quality, productivity, and equipment efficiency. Provide technical leadership, training, and mentorship to process technicians, operators, and other molding personnel. Develop and maintain process documentation ensuring clarity and accessibility for all employees. Provide technical support/solutions to manufacturing processes, improve yield and throughput, drive cost reduction activities, and enhance part quality. Monitor and document issues with injection molds and recommend repairs/refurbishments based on production requirements. Interface with customers and suppliers on technical issues related to molding and/or new projects/processes. Implement technical solutions to meet customer cost, quality, and delivery expectations. Responsible for technical training of all Molding Technicians and associated molding and QC personnel. Perform Risk Assessments and prepare documentation for all new molding projects. Establish, validate, and periodically review process parameters for all molding jobs. Maintain flexible work hours to complete critical mold trials and process validations. Perform Process Capability studies and documentation as required for new tooling and other production equipment. Assist with the planning, purchase, installation, and qualification of new production equipment, including injection machines, automation and robotics, material handling, and related auxiliary equipment systems. Identify and implement continuous improvement projects in molding, assembly, and tooling departments. Work with the QA Department to resolve CARs and associated root cause analysis. Understand and promote ISO 9001 / AS9100 / ISO 13485 Quality System Procedures in all functional areas. Promote Good Manufacturing Practices (GMP) and adherence to company Safety Practices. Must adhere to ITAR regulations. The selected candidate will also possess: Engineering or technical degree desirable. Master Molder and/or Scientific Molding qualifications required. Minimum of 7 years of experience in plastic injection molding. Experience with molded Aerospace and Medical components is desirable. Extensive experience with mold and process validations of plastic injection molded components. Demonstrated ability to start-up, operate, and shut down injection molding machines and related process equipment. Ability to work independently on new process development and troubleshooting current production issues. Strong written and verbal communication skills. DOE (Design of Experiments) CAR (Corrective Action/Root Cause Analysis) SPC (Statistical Process Control) Lean Manufacturing Salary Range: $100k-$115k/yr For immediate and confidential consideration, please email your resume to ******************** or call ************. More information can be found at *****************

Job Title: Senior Manufacturing Engineer Type: Contract - 5 Months - Could Extend Pay:CAN BE FLEXIBLE We are seeking a Sr Manufacturing Engineer for a very important client. Responsibilities may include the following and other duties may be assigned. Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling. Designs arrangement of machines within plant facilities to ensure most efficient and productive layout. Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance. Adapts machine or equipment design to factory and production conditions. May incorporate inspection and test requirements into the production plan. Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality. Develops manufacturing processes that are applicable to statistical process control, and may develop those techniques. Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. Ensures processes and procedures are in compliance with regulations. SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects from design to implementation while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education (typically University). DIFFERENTIATING FACTORS Autonomy: Seasoned individual contributor. Works independently under limited supervision to determine and develop approach to solutions. Coaches and reviews the work of lower level specialists; may manage projects / processes. Organizational Impact: May be responsible for entire projects or processes within job area. Contributes to the completion of work group objectives, through building relationships and consensus to reach agreements on assignments. Innovation and Complexity: Problems and issues faced are difficult, and may require understanding of multiple issues, job areas or specialties . Makes improvements of processes, systems or products to enhance performance of the job area. Analysis provided is indepth in nature and often provides recommendations on process improvements. Communication and Influence: Communicates with senior internal and external customers and vendors. Exchange information of facts, statuses, ideas and issues to achieve objective, and influence decisionmaking. Leadership and Talent Management: May provide guidance, coaching and training to other employees within job area. May manage projects, requiring delegation of work and review of others' work product . Top 3 technical skills that are required for the role: 1. Understanding of various manufacturing processes: This includes knowledge of materials, manufacturing techniques (e.g., injection molding, machining, assembly), and quality control methods. 2. Ability to identify and resolve manufacturing issues: This involves analyzing data, identifying root causes, and implementing effective solutions. 3. Familiarity with statistical process control (SPC) and Six Sigma methodologies. Education Required: Bachelor's in Engineering (Mechanical or Biomedical or Electrical) Years' Experience Required: 4+ years of experience in the Medical Device Manufacturing. Required Knowledge and Experience: Requires advanced knowledge of job area combining breadth and depth, typically obtained through advanced education combined with experience. May have practical knowledge of project management. Requires a University Degree and minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience.

Specific technology/software: Solidworks/Creo (CAD software) Minitab Excel Must haves: Problem solving CAD/drafting skills Technical writing Nice to have skills: Statistical analysis Excel macro coding Power BI Job Summary: This person will be responsible for supplier quality audits, vendor management, and maintaining supplier quality metrics. Will work in a fast paced and dynamic environment where taking initiative and collaborating cross-functionally are critical for success. This role will work in close partnership with Quality, R&D, Operations, Sourcing, and RA. How you will make an impact: Audit, monitor, evaluate, report and improve supplier quality system performance and provide technical support to suppliers Perform supplier evaluations including on-site audits to assess supplier capabilities, determine approval status, and verify corrective action Collect and add supplier information required for the Approved Supplier List Conduct component and product quality testing for purposes of supplier and component qualification and improvement Identify and implement statistical engineering tools and techniques to evaluate supplier process capability and technical performance Evaluate supplier quality systems, strategies, and regulatory compliance via vendor audits Collect and analyze quality metrics relating to Supplier Quality Identify and define correction actions and follow-up to ensure completeness and effectiveness Communicate supplier quality risks to upper management while suggesting improvements and cost savings where possible What you'll need (Required Qualifications): Bachelor's degree in Engineering or Scientific field What else we look for (Preferred Qualifications): Engineering degree Experience with supplier quality engineering activities, including external supplier vendor audits Effective problem-solving techniques (i.e. Root Cause Analysis, FMEA process, Gage R&R, Validation activities, etc.) Conduct effective root cause investigations; assessment of corrective action strategies; and effectiveness as applied to NCRs and SCARs Experience with class II and class III medical devices Medical device, pharma, or biotech industry experience Demonstrated ability to apply statistical quality engineering tools in a supplier environment Working knowledge of International and Domestic FDA regulations Effective communication and conflict resolution skills Thorough understanding of Risk Management principles Strong communication and organizational skills to effectively manage and get results with external suppliers Six Sigma Black Belt/LEAN Manufacturing experience ASQ Certified Quality Engineer or ASQ/BSI Certified Quality Auditor

Senior Process Engineer / Senior Manufacturing Process Engineer Are you ready to drive innovation in manufacturing and help shape the future of sustainable mobility? As a Senior Process Engineer, you'll play a critical role in enhancing existing processes, developing cutting-edge manufacturing solutions, and mentoring a team of passionate professionals. Your contributions will directly impact the quality, efficiency, and success of our manufacturing operations, helping to deliver solutions that improve wellbeing and modern life. Why You Should Apply: Opportunity to work on groundbreaking manufacturing processes in a dynamic and collaborative environment Directly contribute to sustainable solutions that improve mobility and wellbeing Competitive salary range: $120,000 to $140,000 yearly Opportunity to lead and mentor cross-functional teams to drive real change Work with cutting-edge technologies in a rapidly growing field What You'll Be Doing: Improve extrusion processes to enhance safety, quality, and reduce scrap Develop new manufacturing concepts using lean methodologies Lead troubleshooting and root cause analysis for process and equipment issues Mentor and train extrusion technicians and maintenance personnel Drive successful product launches and ensure customer quality and cost requirements are met Develop and update process documentation, including work instructions and troubleshooting guides About You: Be able to do the job as described Strong expertise in thermoplastics extrusion and plastic extrusion processes Experience in root cause analysis and Six Sigma tools (Green or Black Belt preferred) Knowledge of lean manufacturing techniques Excellent communication skills, both written and verbal

BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Process Engineer to work for a leading Orange County area medical device company. **No C2C** Pay Rate: $33-45/hour Contract: 6+ months (possible conversion, depending on experience) Summary The Process Engineer will lead multiple aspects of manufacturing equipment and process design and validation. This position will be responsible for supporting the sustaining manufacturing and operations and working closely with a cross functional team while maintaining equipment uptime and improving upon product cost, quality, and safety. Responsibilities Responsible for developing manufacturing and assembly processes consistent with Design for Manufacturability for new product introductions. Designs, executes and documents process validation protocols in support of quality and regulatory requirements. Provides on-demand pilot line support, managing manufacturing metrics (yields, cycle times, capacity, bottlenecks), ensuring adherence to quality and compliance procedures, identifying and implementing continuous process improvements, deploying new fixture and tooling, and supporting manufacturing documentation updates. Identifies and develops the crucial equipment related to new product development and maintains appropriate uptime for current equipment. Assists pilot line technicians and engineers on manufacturing problems. Purchases and designs equipment that meets safety and environmental requirements. Responsible for communicating business related issues or opportunities to next management level Responsible for ensuring personnel and Company compliance with all Federal, State, local and Company regulations, policies, and procedures. Lead or support troubleshooting activities and process improvements. Perform root cause analysis of failures. Work on special projects as requested by management. Assist with other responsibilities and/or projects as the need arises. Experience/Requirements Bachelor's degree in Mechanical Engineering, Biomedical Engineering or related field is required Minimum of 2 years of industry process engineer experience is required Experience with commercial or pilot manufacturing lines, technical report writing, statistical analysis and data evaluation is required. Knowledge of good manufacturing practices and documentation is required Strong Project Management experience and skills are preferred. Ability to travel up to 10%, international and domestic, required.

I'm currently recruiting for a Senior Photolithography Process Engineer to join a Semiconductor Fab in the LA area. Conducts Design of Experiments (DOE), Failure Mode and Effects Analysis (FMEA), and employee training. Authorizes the release of tools and processes for production, trains and certifies operators, and develops process procedures and work instructions. Defines and executes plans aligned with quarterly objectives. Partners with integration engineers for process development. Supervises process engineers and technicians to ensure tasks are on track. Evaluates process performance and metrology tools. Manages manufacturing processes, tools, and resolves production issues. Job Requirements PhD with 3+ years of industry experience, Master's Degree with 7+ years, or a Bachelor's Degree with extensive hands-on experience. Previous experience working within a wafer fabrication facility. Practical expertise in photolithography processes and metrology tools such as SEM, IVS, and Nanospec. Strong written and verbal communication skills.