Manufacturing engineer jobs in Bellflower, CA

Keysight is on the forefront of technology innovation, delivering breakthroughs and trusted insights in electronic design, simulation, prototyping, test, manufacturing, and optimization. Our ~15,000 employees create world-class solutions in communications, 5G, automotive, energy, quantum, aerospace, defense, and semiconductor markets for customers in over 100 countries. Learn more about what we do. Our, award-winning culture embraces a bold vision of where technology can take us and a passion for tackling challenging problems with industry-first solutions. We believe that when people feel a sense of belonging, they can be more creative, innovative, and thrive at all points in their careers. Responsibilities The Precision Meso-scale Technology Center (PMTC) exists to provide high precision mechanical solutions that enable the capabilities of Keysight's industry leading electronic measurement equipment. As a manufacturing engineer you will develop and sustain manufacturing processes utilizing cutting edge technologies to achieve micron level tolerances in precision machining, specifically turning. We are seeking a hands-on Manufacturing Engineer to support our precision machining operations, with emphasis on CNC Swiss Turning processes. This role is heavily focused on day-to-day shop floor support, working directly with operators and machines to solve production challenges, reduce downtime, and drive continuous improvement. This is not a research, management, or desk-only position-success requires practical machining knowledge, process troubleshooting, and strong collaboration with production staff. Responsibilities As a manufacturing engineer your duties will focus on manufacturing processes of machining (Swiss-type turning), deburring, cleaning, and inspection. Provide real-time troubleshooting and technical support on the production floor for CNC Swiss and conventional turning machines. Develop and maintain setup documentation, work instructions, and process sheets. Optimize machining processes for cycle time, tool life, quality, and cost. Collaborate with operators to address daily challenges in tooling, setups, and dimensional control. Support new product introductions, including process development, machine setup, and first-article documentation. Lead root cause analysis of production issues and implement effective corrective actions. Partner with quality and programming teams to ensure part conformity and efficient production flow Continuous improvement utilizing Lean Tools to analyze and optimize manufacturing processes to improve efficiency, reduce cycle times, and minimize waste and defects. Maintain a commitment to safe working environment and ensuring compliance with all relevant safety regulations. #LI-MO1 Qualifications • Bachelors in Mechanical Engineering, Manufacturing Engineering, or a related field. A Master's degree is a plus. • A minimum of 3-5+ years of applicable experience in precision machining, manufacturing and design (part design, product design, and/or process design). Direct, hands-on experience in a machining environment (shop floor process engineering, setup support, or machine troubleshooting). • Proficiency in developing and improving machining processes for Swiss turning operations, including CNC programming and related tooling. • Solid modeling or 3D CAD proficiency (Solidworks, Creo, Autocad, etc) • Proficiency in interpreting and applying Geometric Dimensioning and Tolerancing (GD&T) standards. • Experience implementing Lean, Six Sigma, DMAIC, and PDCA methodologies to enhance production processes and minimize defects. • Strong analytical and problem-solving abilities to troubleshoot technical issues and devise effective solutions in a fast-paced environment. • Excellent written and verbal communication skills, to include the ability to communicate technical information clearly to non-technical colleagues. Strong documentation skills with the ability to create clear, practical work instructions. • Ability to work in and/or lead diverse cross-functional teams • Strong mechanical aptitude • Excellent organizational and project management skills • Ability to prioritize day to day activities balancing immediate needs with long term project goals This is an on-site position-daily presence on the shop floor is essential. The role involves hands-on problem solving, not primarily academic research, project management, or remote data analysis. The role will be based in Rancho Santa Margarita, CA. (Orange County) Santa Margarita, California pay range: MIN $100,850.00, MIDPOINT $134,460.00 - MAX $168,080.00 Note: For other locations, pay ranges will vary by region This role is eligible for our Keysight Results Bonus Program US Employees may be eligible for the following benefits: Medical, dental and vision Health Savings Account Health Care and Dependent Care Flexible Spending Accounts Life, Accident, Disability insurance Business Travel Accident and Business Travel Health 401(k) Plan Flexible Time Off, Paid Holidays Paid Family Leave Discounts, Perks Tuition Reimbursement Adoption Assistance ESPP (Employee Stock Purchase Plan) Careers Privacy Statement ***Keysight is an Equal Opportunity Employer.*** Keysight Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.

Industry: Medical Devices (Global Aesthetic & Surgical Markets) About Us ELIXIR MD Inc. is a fast-growing fully integrated medical device innovator, headquartered in Irvine, CA. and proud Made in the USA ethos. Our manufacturing, supply, sales and support operations are global with sales in 22 countries (and growing). Our flagship device is transforming the way plastic surgeons practice worldwide. With rapid adoption, global expansion, and highly specialized logistics for a growing portfolio of Devices, We are seeking a Product Design Integration Engineer who is passionate about crafting clean, functional, and human-centered design solutions for healthcare and medical technology products. Role Description The Product Design Integration Engineer will be responsible for designing user experiences and interfaces across Elixir MD's suite of healthcare platforms and applications. This role combines empathy, creativity, and technical understanding to ensure our digital products are accessible, compliant, and aligned with the company's brand and mission. You will collaborate closely with product management, engineering, and clinical teams to translate complex workflows into simple, elegant design solutions that support both patient care and operational excellence. Key Responsibilities User Research & Discovery · Conduct user research and usability testing with clinicians and patients. · Develop personas and journey maps specific to healthcare environments. · Translate user insights into actionable design requirements and interface improvements. Design & Development · Create wireframes, mockups, and interactive prototypes using Figma or similar tools. · Design interfaces optimized for medical environments with a focus on clarity, accessibility, and regulatory compliance. · Collaborate with hardware and electrical engineers on ECAD/MCAD integration, ensuring alignment between physical and digital design. · Maintain and evolve Elixir MD's design system to ensure brand and UX consistency. Collaboration & Implementation · Work closely with product managers, engineers, and clinical advisors to deliver production-ready designs. · Present design concepts to cross-functional teams and incorporate feedback. · Support design reviews, usability validations, and documentation for release. Quality & Iteration · Use testing, analytics, and feedback to continuously refine product designs. · Partner with QA and regulatory teams to uphold design standards for safety and usability. · Stay current with trends in medtech, UX/UI, and digital accessibility. Qualifications · Bachelor's degree in Product Design, Human-Centered Design, UX/UI Design, or related field. · 3-5 years of professional experience as a Product Designer, preferably in healthcare, medtech, or regulated industries. · Proficiency in Figma, Sketch, Adobe XD, or equivalent design software. · Strong understanding of user experience principles, accessibility (WCAG/ADA), and responsive design. · Knowledge of HIPAA compliance and digital health privacy standards preferred. · Excellent collaboration, communication, and presentation skills. · Strong portfolio demonstrating UX/UI design for digital products.

ANEUVO is a platform and therapy development company focused on treating disabling diseases and conditions that are not curable through traditional pharmaceutical approaches. The ANEUVO ExaStim Stimulation System is a non-invasive neuromodulation system that has received CE Mark approval and FDA Breakthrough Device Designation for treating spinal cord injury. ExaStim is currently cleared for use only in Europe, and its use is limited by United States law to investigational purposes. Key Responsibilities: 1) Process Development (In-House) a. Design, develop, and validate in-house manufacturing processes, including assembly, labeling, packaging, and testing. b. Create process documentation such as work instructions, manufacturing travelers, and validation protocols (IQ/OQ/PQ). c. Identify and implement process improvements to enhance quality, efficiency, and yield. d. Support setup and qualification of new equipment, tooling, and fixtures. 2) Contract Manufacturer (CM) Support a. Collaborate with contract manufacturers to transfer processes, troubleshoot production issues, and ensure alignment with company quality and performance standards. b. Review and approve CM process documentation, validations, and change controls. c. Serve as the technical liaison between internal engineering and external manufacturing partners. 3) New Product Introduction (NPI) a. Participate in design reviews to ensure manufacturability and scalability of new designs. b. Support pilot builds, process qualifications, and ramp-up to full production. c. Coordinate process transfer from development to manufacturing. 4) Continuous Improvement & Quality a. Drive continuous improvement through Lean and Six Sigma methodologies. b. Investigate root causes of non-conformances and lead corrective/preventive action implementation. c. Ensure compliance with applicable quality system regulations (e.g., FDA 21 CFR Part 820, ISO 13485). 5) Documentation & Compliance a. Maintain accurate and complete process documentation. b. Support audits and regulatory inspections by providing technical documentation and process evidence. c. Ensure processes meet safety and environmental standards. Qualifications 1) Education: Bachelor's degree in Electrical, Mechanical, Manufacturing, Industrial, or Biomedical Engineering (or equivalent). 2) Experience: 7+ years of experience in manufacturing engineering, preferably within a regulated industry (medical device, pharma, or aerospace). Hands-on experience with process development, validation, and supplier/CM management. 3) Skills: Strong problem-solving and analytical skills. Experience with statistical analysis tools (e.g., Minitab, JMP) and validation methodologies. Proficient in CAD tools and solid understanding of GD&T and design documentation. Excellent communication and project management skills.

Develops and improves manufacturing processes by studying product and manufacturing methods. Evaluates manufacturing processes by designing and conducting research programs; applying knowledge of product design, fabrication, assembly, tooling, and materials; conferring with equipment vendors; soliciting observations from operators. Primary Responsibilities: • Develops manufacturing processes by studying product requirements; researching, designing, modifying, and testing manufacturing methods and equipment; conferring with equipment vendors. • Improves manufacturing efficiency by analyzing and planning work flow, space requirements, and equipment layout. Assures product and process quality by designing testing methods; testing finished- product and process capabilities; establishing standards; confirming manufacturing processes. • Provides manufacturing decision-making information by calculating production, labor, and material costs; reviewing production schedules; estimating future requirements. • Prepares product and process reports by collecting, analyzing, and summarizing information and trends. • Provides manufacturing engineering information by answering questions and requests. • Maintains product and company reputation by complying with government regulations. • Keeps equipment operational by coordinating maintenance and repair services; following manufacturer's instructions and established procedures; requesting special service. • Maintains product and process data base by writing computer programs; entering data. • Completes design and development projects by training and guiding technicians. • Maintains professional and technical knowledge by attending educational workshops; reviewing professional publications; establishing personal networks; participating in professional societies. • Contributes to team effort by accomplishing related results as needed. Must Have Experience: Advanced Manufacturing Engineering

About Us: Spectrum Killian Dental Lab Alliance (SKDLA) is a nationally recognized leader in restorative dentistry, passionate about helping people smile with confidence. We partner with dental professionals across the country to deliver world-class restorations, advanced dental equipment, and trusted services that make a difference for patients every day. At SKDLA, we combine craftsmanship, cutting-edge technology, and a deep commitment to quality to create beautiful, lasting results. More than just a dental lab, we are driven by the belief that every restoration represents a person's confidence, comfort, and well-being - and that's a responsibility we take to heart. Our operations are centered around two advanced Centers of Excellence located in Orange County and Los Angeles. This collaborative environment allows our skilled technicians to innovate, mentor one another, and consistently deliver outstanding results. Overview: The Continuous Improvement & Process Engineer is responsible for analyzing, standardizing, and improving manufacturing and business processes to enhance flow, efficiency, and quality. This role is highly hands-on-working closely with operations, engineering, and quality to map processes, perform time studies, eliminate waste, and implement sustainable improvements. The ideal candidate combines analytical depth, facilitation skills, and a passion for engaging teams in continuous improvement. What You'll Be Responsible For: Process Analysis & Optimization Lead process mapping, value stream mapping, and flow analysis to identify bottlenecks, inefficiencies, and opportunities for improvement. Conduct time studies, work sampling, and line balancing to establish standards and improve productivity. Design and implement single-piece flow, takt time alignment, and standard work to improve reliability and reduce variation. Collaborate with manufacturing and engineering to optimize facility layouts, equipment utilization, and work cell design. Continuous Improvement System Support deployment of the company's Operational Excellence framework, driving measurable improvement in safety, quality, delivery, and cost. Facilitate kaizen events, PDCA cycles, and problem-solving workshops to engage employees in improvement. Use structured methodologies (DMAIC, A3, 8D) to diagnose root causes and drive sustainable corrective actions. Maintain performance visibility through SQDIP boards, KPI dashboards, and daily management systems. Training & Engagement Train and coach team members in Lean manufacturing principles (5S, waste reduction, visual management, standard work). Partner with leaders and operators to develop improvement ideas, document standard work, and sustain gains. Help build a culture of continuous improvement where every employee is a problem solver. Project Management Plan and execute improvement and capital projects, ensuring alignment with business goals and metrics. Track progress using visual project tracking and communicate results through concise, data-driven reporting. Collaborate with cross-functional teams to support new product introduction (NPI), scaling processes for production readiness. Who We're Looking For: Bachelor's degree in Industrial, Manufacturing, Mechanical, or related Engineering discipline. 5+ years of experience in process engineering, industrial engineering, or continuous improvement roles. Strong working knowledge of Lean manufacturing principles, value stream mapping, and time study techniques. Proven experience leading kaizen events and facilitating team-based improvement initiatives. Hands-on ability to collect and analyze process data and implement changes on the production floor. Proficiency in project management, documentation, and structured problem-solving (PDCA, DMAIC, or A3). Strong communication, facilitation, and coaching skills to drive engagement and cultural change. Lean Six Sigma Green Belt or equivalent certification a plus. Experience in regulated manufacturing environments (FDA, ISO 13485, AS9100, or similar), preferred. Familiarity with process validation, capability studies (Cp/Cpk), and statistical analysis tools, preferred. Why SKDLA? Inclusive Environment: We value diversity and are committed to creating a welcoming workplace for individuals of all backgrounds. Career Growth: Spectrum Killian is growing rapidly, offering new opportunities to advance within the company and across promoting internal mobility. Compensation and Benefits: We provide competitive pay and upon conversion to full-time status, employees are eligible to enroll in comprehensive medical, dental, and vision insurance plans. 401K: Full-time employees are also eligible to participate in the company's 401(k) plan with an employer match. Spectrum Killian Dental Lab Alliance is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based on race, religion, color, national origin, gender, gender identity or expression, sexual orientation, age, marital status, veteran status, disability status, or any other protected characteristic under applicable law. The anticipated salary range for this role is $90,000-$110,000. Final compensation will be individually assessed and may differ based on a variety of factors such as your experience, qualifications, education, skill set, certifications, and other relevant considerations. Become part of Spectrum Killian Dental Lab Alliance, a trusted leader in restorative and esthetic dentistry. Work alongside skilled technicians in state-of-the-art facilities to deliver high-quality dental solutions that make a lasting impact. If you're driven by innovation, quality, and continuous growth, we invite you to apply and contribute to the future of dental care!

Kelly Engineering has an outstanding 3-6 month contract Manufacturing Process Engineer position with an industry leader experiencing dynamic growth in Cypress, CA. This position offers a pay rate of $60 per hour and the opportunity to make a significant impact in a fast-paced, technically advanced environment. The Manufacturing Engineer is responsible for automated processes that support the mass production of new and/or existing products. This role will work with automated systems for cutting/heat sealing, lamination, pick-n-place systems, assembly, ultrasonic welding, precision filling, capping, label placement and packaging. Key Responsibilities: Assist in scaling automated and semi-automated solutions based on sound engineering principles. Support initial equipment conceptual development, balancing product specs, process requirements, cost, and lead-time. Collaborate with site and global partners to define and deploy automated processing technologies. Participate in hands-on activities including drafting procedures, executing prototype studies, and authoring technical reports. Work with the Industrialization and Maintenance teams to troubleshoot and resolve equipment or process issues. Qualifications: Strong hands on understanding of automated manufacturing systems and equipment 4+ years of Engineering experience in a manufacturing environment BS degree in a related discipline Strong problem solving and analytical skills What happens next: Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry - even if this position doesn't work out, you're still in the Kelly Engineering network. That means our team of expert engineering recruiters will have access to your profile, making your opportunities limitless.

CADflow is a leading provider of automated 3D design services. Our AI platform prepares 3D models for dental appliance production, producing millions of printable designs every year. Our cloud-based AI platform is available on demand, 24/7 internationally, and accommodates dental labs of all sizes. Job Description: This is a full-time hybrid role for a 3D Machine Learning Engineer at CADflow.ai. You will be responsible for core product development as well as R&D, creating the next generation of custom manufacturing software. You will be working on topics that have never been done before, and must bring both creativity and experience to the team in order to create production-ready code. These products that are used to digitally design 3D files that will be printed and delivered to dental patients around the world. You will also directly field calls and requests from doctors, labs, and other clients. It is mandatory to commute to our El Segundo office 2x a week, with other days being remote optional. Requirements: Experience in pytorch or tensorflow 2+ years Experience with image processing (2D or 3D) Technical bachelors and/or masters Proficient in python 4+ years Additional experience in CI/CD, AWS, React, Three.js, Electron is also helpful Compensation: 160k-210k base benefits: health insurance, dental insurance, vision insurance, 401k match program, unlimited PTO Equity package

Eaton's IS AER FMC division is currently seeking a Lead Manufacturing Engineer in our Los Angeles, California facility! This is an onsite, Monday - Friday role, aligned to a 1st shift schedule. With almost 300 employees, the Los Angeles facility designs and manufactures quality valves, regulators, and other fluid controls used mostly by the Aerospace Industry. The expected annual salary range for this role is $107812.53 - $158125.04 a year. Please note the salary information shown above is a general guideline only. Salaries are based upon candidate skills, experience, and qualifications, as well as market and business considerations. What you'll do: The Lead Manufacturing Engineer role includes the processes, tooling, and equipment to support the production of the fluid controls and actuation product line. This role will provide technical support and implement Lean Manufacturing principles in a production environment. You should have the ability to address technical issues through a problem solving framework with a focus on root cause, containment, and long term solutions. To provide methods of cost reduction for production and production-related activities. In this role you will: Implement Lean Manufacturing principles and utilize Six Sigma methodologies to develop and maintain robust manufacturing processes in order to increase productivity, reduce variation, and eliminate waste Utilize technical skills to troubleshoot and resolve issues related to product non-conformance and performance test failures for hydraulic, pneumatic, and electro-mechanical products. Go to management Lead root cause and correction action for manufacturing issues by utilizing problem solving tools such as 8D analysis and PFMEA's Identify, analyze, and implement cost reduction and productivity improvement projects in a production environment Ability to work on a cross-functional team to execute projects and ensure internal and external customer satisfaction Serve as a technical focal point to operators, team leaders, and other engineers. Serve as a technical contact with internal and external customers, manufacturing, manufacturing engineering, quality assurance, product support, material, and suppliers insuring their satisfaction Develop process plans, fixtures, and tooling in support of Continuous Improvement Processes Research, recommend, and execute capital equipment projects Ensure processes meet Environmental, Safety, and Health (MESH) & regulatory requirements Analyze data from OEM returned products, and implement improvements to increase the processing yield and quality of the components, minimizing the number of returned units Analyze data from mechanical components to implement improvements to increase the producibility of the components, minimizing the assembly and test cycle times Technical expertise on hydraulic and pneumatic products with emphasis on producibility and first time pass Collaborate with peers and management to determine key goals and objectives, and corresponding metrics, to be completed during a determined period (usually one year). Review and amend these actions as appropriate. Focus on timely achievement of these goals and objectives Qualifications: Required Qualifications: Bachelor's degree in Engineering from an accredited institution is required Minimum five years experience in a manufacturing environment This position requires access to export-controlled information. To conform to U.S. Government export regulations applicable to that information, applicant must be a U.S. person, defined as a (i) U.S. citizen or national, (ii) U.S. lawful, permanent resident (green card holder), (iii) refugee under 8 U.S.C. 1157, or (iv) asylee under 8 U.S.C. 1158 Relocation assistance is not available for this position. Only candidates in the immediate geographic area (50 mile radius) of Los Angeles, CA will be considered Preferred Criteria: Previous aerospace experience Masters degree in engineering Position Criteria: Experience with assembly and test operations of hydraulic, pneumatic, or electro-mechanical products. Experience in Lean Manufacturing, Kaizen or other Continuous Improvement Processes. Experience with MRP systems. Familiarity/experience with Six Sigma & Problem Solving methodologies Experience with working on cross-functional teams. Good technical writing, communication, and presentation skills. Proficiency with computer based methods and tools. #LI-CD1 We are committed to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job-related reasons regardless of an applicant's race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, marital status, genetic information, protected veteran status, or any other status protected by law. Eaton believes in second chance employment. Qualified applicants with arrest or conviction history will be considered regardless of their arrest or conviction history, consistent with the Los Angeles County Fair Chance Ordinance, the California Fair Chance Act and other local laws. You do not need to disclose your conviction history or participate in a background check until a conditional job offer is made to you. After making a conditional offer and running a background check, if Eaton is concerned about conviction that is directly related to the job, you will be given the chance to explain the circumstances surrounding the conviction, provide mitigating evidence, or challenge the accuracy of the background report. To request a disability-related reasonable accommodation to assist you in your job search, application, or interview process, please call us at 1-800-###-#### to discuss your specific need. Only accommodation requests will be accepted by this phone number. We know that good benefit programs are important to employees and their families. Eaton provides various Health and Welfare benefits as well as Retirement benefits, and several programs that provide for paid and unpaid time away from work. Click here for more detail: Eaton Benefits Overview. Please note that specific programs and options available to an employee may depend on eligibility factors such as geographic location, date of hire, and the applicability of collective bargaining agreements.

IPS - Rubbercraft is seeking a Manufacturing Engineer 3 - Extrusion, who acts as a key contributor to the NPI Engineering team and supports a variety of complex activities to increase manufacturing capabilities. Actively participates in the introduction of new products to the manufacturing environment. Directly impacts all aspects of safety, quality, delivery, cost, and innovation, as well as the sustaining and growth efforts of operations. About IPS: Integrated Polymer Solutions (IPS) is a leading developer and manufacturer of advanced materials and engineered components, specializing in high-value end markets such as aerospace, defense, medical, semiconductors, robotics, energy, and industrial applications. IPS is comprised of 10 highly respected brands, each recognized for their expertise and innovation: AkroFire, ABBA Roller, Icon Aerospace Technology, IRP Medical, MAST Technologies, Northern Engineering Sheffield (NES), Rubbercraft, Swift Textile Metalizing (STM), RMB Products, and SPIRA Manufacturing. Our extensive product portfolio includes elastomeric seals, gaskets, tooling, hoses, ablatives, survivability tiles, coatings and tapes, EMI and thermal shielding, electrically conductive metalized fabrics, and encapsulated O-rings-all designed to meet the most demanding performance requirements in mission-critical applications. Job Accountabilities: Develops and transfers new products to production ensuring a smooth transition by analyzing product requirements; researching, designing, modifying and testing manufacturing methods and equipment; working with equipment manufacturers. Responsible for all extrusion NPI activities from development to transfer to production Establishes and maintains labor standards to monitor direct/indirect labor and machine performance Assures product and process capability by practical and analytical methods; establishing standards; defining new manufacturing process sequences. Participates in root cause and failure analysis as required and develops with the team root cause and corrective actions. Conduct problem solving efforts and teams with timely and effective troubleshooting, implement productivity improvements, reductions in scrap and rework and waste elimination projects. Support Continuous Improvement initiatives, 6S, and Lean Manufacturing. Interacts with Design Engineering, Operations and Supply Chain teams to ensure design for manufacturability of new products. Participates in design review process and leads manufacturing process development through production implementation. Provides objective, functional, and financial engineering guidance on capital expenditures to division management and follows up on the implementation process Provides knowledge and expertise; acting as a professional resource for colleagues Coordinates all phases of cost reduction; forecasts labor and equipment requirements to assure adequate equipment, machine capacity, and labor This position requires use of information or access to hardware which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. Other responsibilities as assigned. Job Specifications: Education: Bachelor's degree in engineering required Years' Experience: 5+ years of relevant experience required, experience with rubber extrusion Skills: Demonstrated knowledge in extrusion processes and technology Experience with rubber compounding, testing, and mixing equipment Knowledge of rubber manufacturing principles and processes such as compression/transfer molding, injection molding, and tool design Demonstrated expertise with complex manufacturing engineering solutions Thorough knowledge of manufacturing while analyzing, evaluating and determining solutions to a variety of problems Proficient in applying Lean Manufacturing, Six Sigma or other continuous improvement practices Ability to improve products or services by applying professional and business knowledge Able to solve complex problems; makes decisions based on the analysis of multiple sources of information Effective interpersonal, verbal, and written communication skills to drive tasks to completion Proficient in Microsoft Office and Microsoft GP MRP software CAD experience to design fixtures and jigs Benefits: At IPS, we recognize how important your career and benefits are to you and your family. We offer a full suite of benefits including medical, dental, vision, short and long-term disability coverage, accident insurance, critical illness insurance, basic and supplemental life insurance, employee assistance plan, retirement savings and matching, tuition reimbursement and other developmental opportunities. We are committed to supporting the way you live and work. IPS is an Equal Opportunity Employer Veterans/Disabled - Affirmative Action Employer. This position requires the use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee (Actual placement within the salary range is dependent on multiple factors, including but not limited to skills, education, experience and location)

About Us: Precision Tube & Catheter, Inc. (PT&C) is a high-tech enterprise dedicated to manufacturing advanced materials and components for interventional and implantable medical devices. We produce high-quality medical tubes used in various applications, including anesthesiology, respiratory equipment, and biopharmaceutical laboratory equipment. Our commitment to innovation and excellence drives us to exceed industry standards and client expectations. Position Summary: We are Precision Tube & Catheter, Inc. (PT&C), a leader in advanced medical tube manufacturing for interventional and implantable devices. We seek a hands-on Plastic Process Engineer to drive R&D innovation and optimize catheter production processes. This role will design tooling (SolidWorks), lead quality initiatives (NC/CAPA/SCAR), execute FDA validations (IQ/OQ/PQ), and leverage data analytics (Minitab/JMP) to enhance efficiency. The engineer will ensure compliance with GMP/ISO 13485 while collaborating cross-functionally to develop next-generation medical products. Key Responsibilities: Monitor and analyze industry trends and market demands to identify new application opportunities; develop R&D plans aligned with company capabilities. Lead or support the development and optimization of catheter materials and process designs; assess material compatibility with catheter manufacturing processes. Design catheter components and associated tooling-including extrusion dies, injection molds, balloon molds, and fixtures-using SolidWorks. Manage the non-conformance process by driving NC, CAPA, and SCAR activities, including root cause analysis, verification, validation, and implementation of corrective actions. Develop and revise technical documentation such as SOPs, BOMs, Travelers, EFTs (Work Orders), MPIs, NCOs, DHRs, DHFs, FMEAs, Control Plans, and other quality or manufacturing documents. Plan and execute validation activities (IQ/OQ/PQ) for processing equipment and medical device components in compliance with FDA regulations. Perform process verification (OQ/PQ) for the production of extruded components and subassemblies. Analyze data using Minitab or JMP to identify trends, troubleshoot issues, and implement cost improvement projects (CIP) for enhanced efficiency and savings. Manage multiple concurrent projects and lead cross-functional, multi-site teams in the development and optimization of catheter processing and manufacturing. Provide technical support for post-launch production processes and drive continuous improvement initiatives for new product introductions. Define and maintain technical specifications for products, raw materials, and testing methodologies. Stay informed on the latest advancements in polymers, medical device manufacturing, and process engineering; contribute to building the company's R&D knowledge base. Collaborate closely with R&D, Quality, Production, and Supply Chain teams to ensure material and process strategies support product development goals. Ensure compliance with GMP and ISO 13485 standards throughout all activities. Qualifications: Master's degree or higher in Polymer Engineering, Materials Science, Chemical Engineering, or a closely related field. A minimum of 2 years of relevant experience preferred; background in medical device materials or catheter manufacturing is highly desirable. Strong proficiency in polymer processing, including compounding, blending, modification, and testing; working knowledge of plastics processing equipment is required, with hands-on experience preferred. Familiarity with the characterization of polymers and blends used in balloon and tubing applications, including techniques such as DSC, SEM, TEM, Raman Spectroscopy, FTIR, XRF, XRD, X-Ray Tomography, GPC, WAXS, and rheometry. A minor or academic background in Mechanical Engineering is preferred. Bilingual proficiency in Mandarin and English is highly preferred. Working Conditions: Work is conducted in both office and manufacturing environments, requiring compliance with all applicable safety protocols and personal protective equipment (PPE) guidelines. The role may involve prolonged periods of standing and occasional lifting of materials up to 25 pounds, in accordance with applicable workplace safety regulations. Reasonable accommodations may be provided in accordance with the Americans with Disabilities Act (ADA). Benefits / Other: We believe our employees are our greatest resource. We offer a competitive salary and benefits package including 401(k) with employer contribution, paid holidays, and vacation. Insurance coverage includes medical, dental, vision, and prescription drugs. We are proud to be an equal-opportunity workplace. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. If you have a disability or special need that requires accommodation, please let us know. If applying for positions in the U.S., you must be eligible to work in the U.S. without needing an employer-sponsored visa (work permit). Why Join PT&C? At PT&C, you will be part of a dedicated team that values innovation, integrity, and collaboration. As an Extrusion Process/R&D Engineer, you will contribute to the development of cutting-edge medical products that enhance patient care globally. To Apply: Please submit your resume and cover letter to *********************. We look forward to welcoming you to our team! Precision Tube & Catheter, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Note: Fully onsite - Monday - Friday Master's Degree - 0 -2 years industry experience Bachelor's Degree - minimum of 2 years industry experience Nice to have: Tech transfer experience Preferably from BioPharma Industry Ideal candidate: The ideal candidate for this role should have a bachelor's degree in any scientific or engineering discipline with 1 - 3 years professional working experience. Candidates with recent Master degree are also suitable if they bring strong soft skills. The candidate should possess solid working experience with standard software tools such as Microsoft Office. Experience with specialized software such as like SAP or Smartsheets is desirable but can be learned on the job. Biologic drug product knowledge is favorable. The candidate must excel in group management, deadline adherence, and meticulous documentation skills. This position leans heavily on project development (PD) and project management (PM) skills, with technical expertise expected to develop over time. Professional working experience outside of an academic setting is preferred. As a member of the process development team, the candidate will be focused on supporting senior staff to develop and characterize drug product technologies and manufacturing capabilities, as well as assist in the process validation and technology transfer of multiple Amgen products to the aseptic fill finish manufacturing plants at Amgen Thousand Oaks which includes various production lines. The candidate will support senior staff in the planning, execution, and documentation of characterization, process validation and technology transfer projects. The candidate will be primarily responsible for supporting execution of characterization studies to generate technical data packages using complex technology, organization of data and analysis of results, and compiling information in concise summaries while under supervision of senior staff. The candidate will be responsible for interfacing with various drug product teams to ensure successful technology transfer and completion of associated technical documentation for Amgen products. The candidate will assist with experimental design, develop and execute protocols, obtain reproducible and reliable results, analyze and document experimental results, and communicate results to cross-functional groups. Preferred Qualifications: • B.S. in scientific or engineering discipline with 1‒3 years' relevant professional experience or M.S. in scientific or engineering discipline with 0‒2 years' relevant professional experience • Familiarity with cGxP and experience in drug product / drug substance manufacturing or process development • Knowledge of and hands-on experience with various drug product technologies • Displays critical thinking, problem solving and independent research skills • Ability to learn new techniques, perform multiple tasks, keep accurate records, follow instructions, and comply with company policies • Excellent project management skills and ability to escalate relevant issues to project lead and line-management • Strong cross functional team player with good communication skills (oral and written) • Ability to work independently and as part of a team with internal and external partners • Good computer and organizational skills with strong attention to detail • Self-motivated with a positive attitude

The Senior Quality Engineer will focus on implementing and optimizing quality engineering practices related to complaints investigation, post-market surveillance, and risk management. This role ensures compliance with global regulatory requirements while fostering a culture of quality across all product lines. Job Responsibilities In this role, you will manage and support a variety of projects within the Quality Engineering department. Key responsibilities include: Investigate complex manufacturing quality and compliance issues (e.g., CAPA, non-conformances, audit observations) based on engineering principles. Execute complaint investigations using a multifunctional, systematic approach to resolve issues effectively and in compliance with procedures. Lead post-market surveillance activities for approved products, ensuring all complaints are properly tracked and completed on time. Develop, update, and maintain technical content for risk management files. Collaborate with investigation owners and cross-functional teams to address overdue cases and enhance investigation quality. Analyze data, make recommendations, and generate detailed reports based on investigation findings. Identify and implement opportunities for process improvements and efficiency within quality systems. Knowledge & Skills Strong documentation, communication, and interpersonal relationship skills. Proficiency in Microsoft Office Suite (including MS Project) and electronic quality management systems. Fundamental understanding of statistical techniques and engineering principles. Strong problem-solving, analytical, and critical-thinking skills. Familiarity with FDA regulations and quality system requirements for medical devices. Ability to manage multiple priorities and work effectively in fast-paced environments. Excellent collaboration skills with the ability to influence and lead change. Strict attention to detail and adherence to company safety and compliance protocols. Education & Experience Bachelor's degree in Engineering required. 5-7 years of relevant experience. Experience in the medical device industry preferred. ...

Lee Spring is seeking Manufacturing Engineering Technician to join our Headquarters' team. About us: Lee Spring manufactures and distributes mechanical springs, wire forms, stampings and fourslide parts worldwide. We offer an extensive product line of more than 25,000 inventoried products in a variety of materials available in stock and ready to ship today. In addition, we also manufacture springs made to customer specifications. Lee Spring is the premier global source for stock catalog and custom designed mechanical springs and related products. Founded by Robert Lee Johannsen in 1918, Lee Spring began in Brooklyn New York and our Global Headquarters are still based in Brooklyn today. Through the years, we have expanded with additional strategic locations throughout the United States, Europe, Latin America and Asia. We are well known for our extensive and comprehensive catalog of stock springs that have been used by engineers, professionals and buyers for decades. Beyond the catalog, we have considerable custom spring capabilities, personnel and a proficiency that comes with our many years within the industry. The manufacturing engineer position provides a crucial link between customer requirements and the final product that we deliver to our customers. The manufacturing engineer helps to define product specifications, develop and implement cost-effective manufacturing processes, and coordinate overall manufacturing/sourcing methods for both new and existing products. Duties and Responsibilities: Interpretation of customer production specifications in the form of drawings (blueprints), text, samples or application requirements. Analysis of product material and configuration specifications to determine suitability of form, fit and function. Analysis of product specification and tolerance with regards to quality versus manufacturing process capabilities. Determination of the manufacturing process including product structure (bill of materials), manufacturing routing(s), outside service processes and the application of manufacturing engineering standards. Definition of product and raw material stock codes including description, invoked industry standards and revision levels. Preparation of cost estimates in support sales and customer service to determine prices and subsequently acknowledge quotations to customers. Preparation of factory documentation including drawings. Design and development of primary and alternate manufacturing processes capable of complying with product design requirements. Definition and application of product scheduling, parameters including calculation of lead time, definition of economic or other batch quantities and determine of material supply requirements. Interfacing with production system and quality system personnel. Job Requirements Bachelor's in industrial or mechanical engineering. 3-5 years of related experience Knowledge of mechanical manufacturing processes, including assembly and testing. Strong leadership skills. Excellent verbal and written communication skills. Fluency in written and spoken English. Lee Spring Company provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, we also comply with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfers, leaves of absence, compensation and training. We offer a generous benefits package, which includes -Medical Insurance -Dental -Vision -Short & Long Term Disability -Cancer Coverage -Accident Coverage -Life Insurance -Paid Time Off -Vacation Days -10 Paid Holidays - 401k Plan - And many more

R&D Sustaining Engineer | Medical Devices Compensation: $100k-$120k + bonus + benefits Employment: Full Time (This role is not eligible for visa sponsorship.) We are seeking an R&D Engineer who thrives in solving problems, improving products, and collaborating cross-functionally. This role focuses on supporting and improving existing medical device products - ensuring they remain reliable, compliant, and cost-effective throughout their lifecycle. You'll work closely with Manufacturing, Quality, Supply Chain, and Regulatory teams to troubleshoot issues, implement design changes, and drive continuous improvement efforts. What You'll Do Lead sustaining engineering projects focused on product improvements, cost reductions, and component updates Serve as a primary R&D partner to Manufacturing for troubleshooting and root cause analysis Implement and document design & process changes in compliance with regulated environments Support V&V testing, documentation, and engineering evaluations Contribute to change orders, labeling/IFU updates, and competitive product testing What You Bring Bachelor's degree in Mechanical, Biomedical, Electrical, or related engineering field 4+ years in a regulated industry; medical device experience strongly preferred Understanding of FDA, ISO, and GMP requirements Experience with design controls, risk management, and validation Strong problem-solving and project leadership skills Proficiency with SolidWorks and Microsoft Office / MS Project Familiarity with lean manufacturing or continuous improvement methodologies

The Electrical Manufacturing Engineer is responsible for maintaining the efficiency and effectiveness of all related manufacturing equipment & processes required to manufacture a high quality product costs in mind. RESPONSIBILITIES: • Primary responsibility is to provide Manufacturing Engineering support to resolve any manufacturing or related issues on sustaining and new products • Implement processes to increase improvements in all related manufacturing processes • Troubleshooting and technical support to address product issues and processes • Support the transition of products from development to volume production • Resolves production issues on the spot while ensuring design integrity allowing us to stay on schedule • Facilitate a close relationship with the engineering team during design, build, and test to provide design feedback • Determine schedule impacts for unforeseen design or process changes in production • Provide clear communication between the design engineering team and the production floor • Concerning product tooling, confer with engineering teams and suppliers to ensure efficient production methods and schedules • Utilize lean manufacturing tools; recommend improvements in production methods, standards, tooling, equipment, layout, procedures, product designs, and employee efficiency • Identify continuous improvement opportunities for yield, performance, and cost • Work with the design team in response to manufacturing problems, parts obsolescence, and minor requirement changes • Prepare and maintain documentation required to ensure efficient production PREFERRED SKILLS AND EXPERIENCE: BS degree in Electrical Engineering (Desired), Manufacturing Engineering, Mechanical Engineering or similar field or equivalent experience as an Engineer in these fields required 5+ years of experience in Electrical, Test, Manufacturing, Mechanical Engineering or similar field in Aerospace, Automotive, or Commercial industries; or 3 years with a Masters Degree Specific experience with printed circuit board assembly, electro-mechanical assembly, calibration and testing processes is desired Organization/planning, communication (oral and written), time management, conflict management, ability to manage stress, deadlines and work independently Software Knowledge: Microsoft Office, AutoCAD, SolidWorks. BENEFITS: AeroAntenna offers a great benefits package, included but not limited to 401K with company matching up and vacations. What we do: The company ( Now is a part of HEICO Corp .) is a leader in the design and production of high performance active antenna systems for critical defense applications, precision guided munitions, commercial aircraft and other commercial uses. Antenna types it makes include GPS, aircraft navigation and satellite communications antennas. Additional Information: • Job Site: 20732 Lassen Street, Chatsworth, CA 91311 • Mail Resumes To: ATTN: HR, AeroAntenna Technology, Inc., 20732 Lassen Street, Chatsworth, CA 91311 • eMail Resumes To: [email protected]

The main function of a Sr Engineer in this quality role is to focus on implementing and optimizing quality engineering practices related to Complaints Investigation, Post Market Surveillance and Risk Management while ensuring a culture of quality and compliance with global regulatory requirements. Education and Experience: Bachelor's degree in engineering required. 5-7 years of experience required. Skills: Proven expertise in the usage of MS Office Suite including MS Project; Electronic Quality Management System. Strong documentation, communication (e.g., written and verbal) and interpersonal relationship skills including consultative and relationship management skills Basic understanding of statistical techniques Team player and detail-oriented. Substantial understanding and knowledge of principles, theories, and concepts relevant to Engineering Strong problem-solving, organizational, analytical and critical thinking skills Substantial understanding of processes and equipment used in assigned work Good leadership skills and ability to influence change Knowledge of applicable FDA regulations for the medical device industry Strict attention to detail Ability to interact professionally with all organizational levels Ability to manage competing priorities in a fast-paced environment Must be able to work in a team environment, including inter-departmental teams and key contacts representing the organization on contracts or projects Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of the environment and prevention of pollution under their span of influence/control Job Responsibilities: Investigate complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) based on engineering principles; analyze results, make recommendations and develop reports. Execute complaint investigations multifunctional approach and address issues addressed in a systematic, methodical manner. Lead Post Market Surveillance activities for products approved in the EU. Oversight of all complaints that require investigation through the different phases. Ensure on-time completion of complaints. Work closely with complaint investigation owners to resolve issues and ensure those that have passed their due dates are addressed. Ensure complaint investigations are adequate and comply with applicable procedures. Develop, update, and maintain technical content of risk management files Other incidental duties assigned by Leadership

Job Description Template: ATR International is a widely renowned technical staffing and consulting leader. Our firm has grown to serve a range of companies-from startups to Fortune 500 organizations. And we support a plethora of industries, from IT, engineering, telecommunications, and finance to healthcare, insurance, and retail. By bringing passion for excellence, trust, and inclusion to every interaction, we build deep connections with our clients, contractors, and local markets to drive long-term mutual success. Our passion for inclusion is at the heart of our success. Our woman-led, minority-owned firm welcomes fresh perspectives, and our efforts have earned us WBENC Certification-the most prestigious national recognition for women-owned businesses in the U.S. Today, ATR remains one of the most diverse firms in the staffing industry. As a Quality Engineer, you will play a key role in ensuring that products and processes comply with regulatory and Client standards. You'll collaborate cross-functionally to drive continuous improvement, support manufacturing, and ensure the highest levels of product quality and patient safety. The role includes hands-on support in controlled environments, involvement with animal-origin tissue, and active participation in daily production activities. Job Title Responsibilities: Provide quality engineering support for manufacturing, sustaining, and new product introduction. Participate in daily manufacturing tier meetings to support production and address quality-related concerns. Be present in controlled environment areas/clean rooms to monitor processes, support investigations, and ensure compliance with quality standards. Work with tissue from animal origin (porcine and bovine) in accordance with safety and regulatory requirements. Investigate product non-conformances and implement corrective and preventive actions (CAPA). Lead or participate in process validation activities (IQ/OQ/PQ). Ensure compliance with FDA QSR, ISO 13485, and other applicable regulations. Review and approve process and product changes. Analyze data, conduct risk assessments, and support root cause analysis. Lead or support internal and external audits. Participate in the development and review of quality documentation (procedures, protocols, reports). Requirements: Bachelor's degree in Engineering, Science, or related technical field. 4+ years of experience in Quality Engineering or a related field in the medical device or regulated industry. Experience with Nonconformance material reports, CAPAs, and FMEA. Able to work with Bovine and Porcine tissue. Working knowledge of FDA regulations and ISO 13485. Preferred Qualifications: Experience with CAPA, risk management (FMEA), and process validation. ASQ certification (CQE, CQA) a plus. Strong communication and teamwork skills. Experience with statistical analysis and data interpretation.

HCLTech is looking for a highly talented and self- motivated R&D Engineer / Mechanical Engineer to join it in advancing the technological world through innovation and creativity. Job Title: R&D Engineer / Mechanical Engineer Job ID: 1626464BR Position Type: Full Time with HCLTech Location: Irvine, CA ( Onsite ) Role/Responsibilities Good in SolidWorks (1 to 2 years) Windchill Change management experience Medical Device Product development Validation & Verification (V&V) Good in communication and interpersonal skills Qualifications & Experience Minimum Requirements Bachelor's degree in relevant field Pay and Benefits Pay Range Minimum: $40.38 per hour Pay Range Maximum: $47.00 per hour HCL is an equal opportunity employer, committed to providing equal employment opportunities to all applicants and employees regardless of race, religion, sex, color, age, national origin, pregnancy, sexual orientation, physical disability or genetic information, military or veteran status, or any other protected classification, in accordance with federal, state, and/or local law. Should any applicant have concerns about discrimination in the hiring process, they should provide a detailed report of those concerns to ****************** for investigation. Compensation and Benefits A candidate's pay within the range will depend on their work location, skills, experience, education, and other factors permitted by law. This role may also be eligible for performance-based bonuses subject to company policies. In addition, this role is eligible for the following benefits subject to company policies: medical, dental, vision, pharmacy, life, accidental death & dismemberment, and disability insurance; employee assistance program; 401(k) retirement plan; 10 days of paid time off per year (some positions are eligible for need-based leave with no designated number of leave days per year); and 10 paid holidays per year. How You'll Grow At HCLTech, we offer continuous opportunities for you to find your spark and grow with us. We want you to be happy and satisfied with your role and to really learn what type of work sparks your brilliance the best. Throughout your time with us, we offer transparent communication with senior-level employees, learning and career development programs at every level, and opportunities to experiment in different roles or even pivot industries. We believe that you should be in control of your career with unlimited opportunities to find the role that fits you best.

Advanced Cooling Technologies, Inc. (ACT) is a premier thermal solutions provider providing component and system level solutions and structures. Our products and technologies have become integral parts of numerous mission-critical devices, including life-saving MRI and CT scanners, US Military applications, weather and telecommunication satellites, exploratory space missions, and much more. We are proud to be doing work that really makes a difference in our world- and beyond! Manufacturing Engineer - Satellite Structures As a Manufacturing Engineer specializing in Satellite Structures, you will lead project management activities while collaborating closely with customers and production teams to ensure program success. Our work environment demands a candidate with the ability to take on multiple responsibilities in a fast-paced environment. We are looking for team players who enjoy working with customers, vendors, and co-workers to provide the best service and solutions. The best candidates will be those who embrace new challenges, using critical thinking skills, and developing innovative solutions. Primary Responsibilities: Manage schedules, resources, and deliverables for complex composite manufacturing projects. Drive program execution from planning through delivery, ensuring alignment with customer requirements and budget. Support secondary activities in design, manufacturing, quality assurance, tooling, and materials as needed. Frequent customer communication/interaction Hands-on experience with design for manufacturability (DFM) and prototype hardware fabrication and testing is a plus! We offer an attractive and competitive compensation/benefits package, which includes a profit-sharing bonus plan. Our work environment is comfortable, collaborative, and stimulating. Apply now to get started on a career with ACT! If you are looking for an opportunity to start a career with a growing company doing exciting and important work, please apply today! ACT is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as a qualified individual with a disability, or any other trait protected by law. E-verify employer. Requirements B.S. or M.S. degree in Mechanical Engineering or Aerospace Engineering. Knowledge of Advanced Fiber-Reinforced and/or Aluminum Honeycomb Composites and associated manufacturing methods. Ability to operate in a fast-paced environment and contribute immediately upon hire. Must be a US Person as defined by 22 C.F.R. §120.15? (U.S. Citizen, lawful permanent resident, refugee or asylee.) Salary Description $80,000 to $120,000