Process engineer jobs in White Plains, NY - 204 jobs

The Senior Casting Technology Manufacturing Engineer provides technical leadership for SX or equiax investment castings across the value stream. You will partner with suppliers and cross-functional teams to drive root cause problem solving, improve producibility, increase productivity, and deliver on business objectives. You will own supplier technical relationships, coach on internal processes/specs/methods, qualify new suppliers, and help develop and industrialize alternate casting technologies. **Job Description** **Roles and Responsibilities** + Provide process and product technical leadership for the Castings commodity, including SX or equiax investment castings. + Develop strong working relationships with casting supplier technical teams. + Partner with suppliers to identify and implement corrective actions to eliminate the cause and prevent recurrence. + Act as a change agent to advance world-class performance and standard work across the supply base. + Own supplier technical relationships; mentor suppliers on GE Aerospace processes, specifications, and methods; ensure compliance and capability. + Lead cross-functional problem solving, to identify true root cause and implement sustainable corrective and preventive actions. + Improve manufacturability through design-for-casting, specification clarity, and process capability improvements. + Clearly communicate progress, risks, challenges, and countermeasures to leadership and stakeholders. + Review and approve significant/special processes; ensure adherence to standards and qualification requirements. + Collaborate with Quality and Design Engineering to ensure new and changed processes meet established metrics; align with other commodities on strategy and objectives + Partner with suppliers and internal teams to interpret drawings/specifications, ensuring conformance and clarity. + Identify and onboard new suppliers; lead technical qualifications and readiness through Manufacturing and Quality Planning reviews and support supplier Castings Audits. + Ability to travel to supplier sites 30%-50% **Minimum Required Qualifications** + Bachelor's degree in Engineering (Materials/Metallurgy, Mechanical, Manufacturing, or related field) + Minimum of 5 years of materials engineering, castings, mechanical engineering or a related field **Desired Characteristics and Experience** + Additive manufacturing experience. + Metal Injection Molding (MIM) experience. + Proficiency with Siemens NX or comparable CAD. + Sand Castings Experience. + Titanium Experience. + Significant experience in investment castings (SX or equiax), with demonstrated yield, capability, and cost improvements + Hands-on expertise across investment casting special processes (wax, shell, melt/solidification control, heat treat, HIP, NDT) and specification compliance. + Strong problem solving and project management skills. + New Product Introduction experience. + Experience maturing technologies and processes. + Excellent communication and stakeholder management; ability to influence without authority + Humble learner: Respectful, receptive to feedback, agile, and continuously improving; seeks out diverse perspectives. + Transparent communicator: Shares critical information proactively; speaks with candor; engages constructively to resolve issues. + Focused and accountable: Fast learner with strong ownership; meets commitments and drives results against SQDC targets ( _Safety, Quality, Delivery and Cost in that order)_ . **Pay and Benefits:** + The salary range for this position is $ 116,000.00 - 155,000.00. The specific salary offered to a candidate may be influenced by a variety of factors including the candidate's experience, their education, and the work location. In addition, this position is eligible for a performance bonus/variable incentive plan. + GE provides a comprehensive benefits package that provides access to plans which support the overall wellbeing of our employees and their dependents. These benefits include, but are not limited to, health care coverage (medical, dental, vision, pharmacy), a retirement plan that includes Company Retirement Savings and a 401K with Company matching, Life Insurance options, Disability coverage, paid time-off, EAP, and more. Healthcare benefits include medical, dental, vision, and prescription drug coverage; access to a Health Coach, a 24/7 nurse-based resource; and access to the Employee Assistance Program, providing 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Retirement Savings Plan, a tax-advantaged 401(k) savings opportunity with company matching contributions and company retirement contributions, as well as access to Fidelity resources and planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability insurance, life insurance, and paid time-off for vacation or illness. General Electric Company, Ropcor, Inc., their successors, and in some cases their affiliates, each sponsor certain employee benefit plans or programs (i.e., is a "Sponsor"). Each Sponsor reserves the right to terminate, amend, suspend, replace, or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a Sponsor's welfare benefit plan or program. This document does not create a contract of employment with any individual. GE Aerospace offers comprehensive benefits and programs to support your health and, along with programs like HealthAhead, your physical, emotional, financial and social wellbeing. Healthcare benefits include medical, dental, vision, and prescription drug coverage; access to a Health Coach from GE Aerospace; and the Employee Assistance Program, which provides 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Aerospace Retirement Savings Plan, a 401(k) savings plan with company matching contributions and company retirement contributions, as well as access to Fidelity resources and planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability insurance, life insurance, and paid time-off for vacation or illness. GE Aerospace (General Electric Company or the Company) and its affiliates each sponsor certain employee benefit plans or programs (i.e., is a "Sponsor"). Each Sponsor reserves the right to terminate, amend, suspend, replace or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a Sponsor's welfare benefit plan or program. This document does not create a contract of employment with any individual. _This role requires access to U.S. export-controlled information. Therefore, employment will be contingent upon the ability to prove that you meet the status of a U.S. Person as one of the following: U.S. lawful permanent resident, U.S. Citizen, have been granted asylee or refugee status (i.e., a protected individual under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3))._ **Additional Information** GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer (****************************************************************************************** . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). **Relocation Assistance Provided:** No \#LI-Remote - This is a remote position GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Welcome to Haleon. We're a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we've grown, evolved and are now entering an exciting new chapter - one filled with bold ambitions and enormous opportunity. Our trusted portfolio of brands - including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum - lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science. Now it's time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose - to deliver better everyday health with humanity - at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture. Hello. We're Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we're improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands - including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum - through a unique combination of deep human understanding and trusted science. What's more, we're achieving it in a company that we're in control of. In an environment that we're co-creating. And a culture that's uniquely ours. Care to join us. It isn't a question. With category leading brands such as Sensodyne, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise, we're uniquely placed to do this and to grow a strong, successful business. This is an exciting time to join us and help shape the future. It's an opportunity to be part of something special. About the role The Reliability Engineer plays a critical role in ensuring the reliability and optimal performance of manufacturing equipment. This position is responsible for developing, implementing, and maintaining reliability strategies to reduce downtime, increase equipment availability, and optimize the performance of critical assets. The Reliability Engineer will lead efforts in Preventive Maintenance (PM) optimization, Root Cause Analysis (RCA), and continuous improvement initiatives while collaborating with cross-functional teams to support the overall maintenance and reliability strategy. Role Responsibilities * Preventive Maintenance (PM) Optimization: Responsible for reliability of production equipment on site and Reliability KPIs, (MTTR) and (MTBF). * Root Cause Analysis (RCA): Responsible for ensuring effective troubleshooting and reoccurrence elimination of breakdowns. * Reliability Improvement Initiatives: Recommend improvements and desirable modifications in methods, procedures, processes, facility/equipment, and layout. * Maintenance Planning and Scheduling: Support the maintenance planning and scheduling processes by providing input on equipment criticality and PM task prioritization. * Spare Parts and Inventory Management: Responsible for developing stock of critical spare parts within budget targets. * Data Analysis and Reporting: Fluent use of the site's CMMS system. * Training and Development: Responsible for coaching & executing the Preventative Maintenance strategy for the site. This will be based on TPM, AM and other industry standards. * Cross-Functional Collaboration: Work with managers effectively to execute the policies and goals of the organization. Author, review, revise, or approve Standard Operating Procedures and Change Controls as required. Why you? Basic Qualifications: * Bachelor's degree in Mechanical Engineering, Electrical Engineering, or equivalent * 5 to 10 years Maintenance experience required. * Minimum of 5 years' experience in reliability engineering related processes. * Prefer 5 years of experience in cGMP industry * Expertise in multiple areas of maintenance and reliability, material management, planning and scheduling, and CMMS / EAM / ERP optimization. * Effective communication skills and practices and have experience with reliability productivity tools. * Understand the RCM process, failure mode identification, defect analysis, cause and effect analysis, loss elimination, determination of probability, and consequence of failures; along with the use of sFMEA, RCFA decision logic, and writing tasks to mitigate identified failures. * Demonstrate knowledge of generic problem solving, and the RCA process. * Strong mechanical and electrical knowledge. * Have a solid knowledge of equipment assembly, installation, and repair. * Familiarity with asset Management, its various components and organization. * Understand condition monitoring principles, tools, and application. * Ability to communicate/teach reliability best practices, condition monitoring, and precision methods. Preferred Qualifications * Computer knowledge (Excel, Word, Power Point) * Good communication skills. * Understanding of Root Cause Analysis. * Computer Maintenance Management System knowledge (CMMS - e.g. SAP). Haleon offers a robust Total Reward package that consists of competitive pay and a comprehensive benefits program. This includes a generous 401(k) plan, tuition reimbursement and time off programs including 6 months paid parental leave. On day one, you are eligible for benefits, including our healthcare programs where the company pays for the majority of your medical coverage for you and your family. We also offer the opportunity to receive a discretionary bonus based on the achievement of key business performance and other incentive/recognition programs as part of the offering. The salary range for this position is: $102,921 to $141,517 annually plus a 12% Performance Bonus Benefits Haleon offers a robust Total Reward package that consists of competitive pay and a comprehensive benefits program. This includes a generous 401(k) plan, tuition reimbursement and time off programs including 6 months paid parental leave. On day one, you are eligible for benefits, including our healthcare programs where the company pays for the majority of your medical coverage for you and your family. We also offer the opportunity to receive a discretionary bonus based on the achievement of key business performance and other incentive/recognition programs as part of the offering. Job Posting End Date 2026-01-26 Equal Opportunities Haleon are committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. It guides us in creating an inclusive culture, where different backgrounds and views are valued and respected - all in support of understanding and best serving the needs of our consumers and unleashing the full potential of our people. It's important to us that Haleon is a place where all our employees feel they truly belong. During the application process, we may ask you to share some personal information, which is entirely voluntary. This information ensures we meet certain regulatory and reporting obligations and supports the development, refinement, and execution of our inclusion and belonging programmes that are open to all Haleon employees. The personal information you provide will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment decisions, including hiring decisions. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, Haleon may be required to capture and report expenses Haleon incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure Haleon's compliance to all federal and state US Transparency requirements. Accommodation Requests If you require a reasonable accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please contact us by sending an email to ***************************. Please include the following in your email: Use subject line: 'Haleon Careers: Job Accommodation Request' Your Name and contact information Requisition ID and Job Title you are interested in Location of Requisition (city/state or province/country) Description of specific accommodation you are requesting Please note: Resumes, CVs, or other requests outside of accommodation support submitted to this email box will not be accepted. Note to candidates The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.

Welcome to Haleon. We're a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we've grown, evolved and are now entering an exciting new chapter - one filled with bold ambitions and enormous opportunity. Our trusted portfolio of brands - including Sensodyne , Panadol , Advil , Voltaren , Theraflu , Otrivin , and Centrum - lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science. Now it's time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose - to deliver better everyday health with humanity - at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture. Hello. We're Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we're improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands - including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum - through a unique combination of deep human understanding and trusted science. What's more, we're achieving it in a company that we're in control of. In an environment that we're co-creating. And a culture that's uniquely ours. Care to join us. It isn't a question. With category leading brands such as Sensodyne, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise, we're uniquely placed to do this and to grow a strong, successful business. This is an exciting time to join us and help shape the future. It's an opportunity to be part of something special. About the role The Reliability Engineer plays a critical role in ensuring the reliability and optimal performance of manufacturing equipment. This position is responsible for developing, implementing, and maintaining reliability strategies to reduce downtime, increase equipment availability, and optimize the performance of critical assets. The Reliability Engineer will lead efforts in Preventive Maintenance (PM) optimization, Root Cause Analysis (RCA), and continuous improvement initiatives while collaborating with cross-functional teams to support the overall maintenance and reliability strategy. Role Responsibilities Preventive Maintenance (PM) Optimization: Responsible for reliability of production equipment on site and Reliability KPIs, (MTTR) and (MTBF). Root Cause Analysis (RCA): Responsible for ensuring effective troubleshooting and reoccurrence elimination of breakdowns. Reliability Improvement Initiatives: Recommend improvements and desirable modifications in methods, procedures, processes, facility/equipment, and layout. Maintenance Planning and Scheduling: Support the maintenance planning and scheduling processes by providing input on equipment criticality and PM task prioritization. Spare Parts and Inventory Management: Responsible for developing stock of critical spare parts within budget targets. Data Analysis and Reporting: Fluent use of the site's CMMS system. Training and Development: Responsible for coaching & executing the Preventative Maintenance strategy for the site. This will be based on TPM, AM and other industry standards. Cross-Functional Collaboration: Work with managers effectively to execute the policies and goals of the organization. Author, review, revise, or approve Standard Operating Procedures and Change Controls as required. Why you? Basic Qualifications: Bachelor's degree in Mechanical Engineering, Electrical Engineering, or equivalent 5 to 10 years Maintenance experience required. Minimum of 5 years' experience in reliability engineering related processes. Prefer 5 years of experience in cGMP industry Expertise in multiple areas of maintenance and reliability, material management, planning and scheduling, and CMMS / EAM / ERP optimization. Effective communication skills and practices and have experience with reliability productivity tools. Understand the RCM process, failure mode identification, defect analysis, cause and effect analysis, loss elimination, determination of probability, and consequence of failures; along with the use of sFMEA, RCFA decision logic, and writing tasks to mitigate identified failures. Demonstrate knowledge of generic problem solving, and the RCA process. Strong mechanical and electrical knowledge. Have a solid knowledge of equipment assembly, installation, and repair. Familiarity with asset Management, its various components and organization. Understand condition monitoring principles, tools, and application. Ability to communicate/teach reliability best practices, condition monitoring, and precision methods. Preferred Qualifications Computer knowledge (Excel, Word, Power Point) Good communication skills. Understanding of Root Cause Analysis. Computer Maintenance Management System knowledge (CMMS - e.g. SAP). Haleon offers a robust Total Reward package that consists of competitive pay and a comprehensive benefits program. This includes a generous 401(k) plan, tuition reimbursement and time off programs including 6 months paid parental leave. On day one, you are eligible for benefits, including our healthcare programs where the company pays for the majority of your medical coverage for you and your family. We also offer the opportunity to receive a discretionary bonus based on the achievement of key business performance and other incentive/recognition programs as part of the offering. The salary range for this position is: $102,921 to $141,517 annually plus a 12% Performance Bonus Benefits Haleon offers a robust Total Reward package that consists of competitive pay and a comprehensive benefits program. This includes a generous 401(k) plan, tuition reimbursement and time off programs including 6 months paid parental leave. On day one, you are eligible for benefits, including our healthcare programs where the company pays for the majority of your medical coverage for you and your family. We also offer the opportunity to receive a discretionary bonus based on the achievement of key business performance and other incentive/recognition programs as part of the offering. Job Posting End Date2026-01-26 Equal Opportunities Haleon are committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. It guides us in creating an inclusive culture, where different backgrounds and views are valued and respected - all in support of understanding and best serving the needs of our consumers and unleashing the full potential of our people. It's important to us that Haleon is a place where all our employees feel they truly belong. During the application process, we may ask you to share some personal information, which is entirely voluntary. This information ensures we meet certain regulatory and reporting obligations and supports the development, refinement, and execution of our inclusion and belonging programmes that are open to all Haleon employees. The personal information you provide will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment decisions, including hiring decisions. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, Haleon may be required to capture and report expenses Haleon incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure Haleon's compliance to all federal and state US Transparency requirements. Accommodation Requests If you require a reasonable accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please contact us by sending an email to ***************************. Please include the following in your email: Use subject line: ‘Haleon Careers: Job Accommodation Request' Your Name and contact information Requisition ID and Job Title you are interested in Location of Requisition (city/state or province/country) Description of specific accommodation you are requesting Please note: Resumes, CVs, or other requests outside of accommodation support submitted to this email box will not be accepted. Note to candidates The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Various outside weather conditions, Will work with hazardous/toxic materials, Working at heights Job Description The Engineer II, Manufacturing at Thermo Fisher Scientific Inc. will play an exceptionally crucial role in refining production processes within our Lab Chemical Division (LCD). This role involves close collaboration with equipment engineering, safety, quality, and operational units to develop and implement projects that aim to boost efficiency and reduce costs. Key Responsibilities Provide technical support for production operations, ensuring reliable, safe, and efficient manufacturing. Collaborate with production teams to resolve complex process-related issues and improve stability. Develop and implement manufacturing processes that improve efficiency, quality, and sustainability. Work with maintenance, operations, and process engineering teams to identify improvement opportunities and implement changes. Develop and maintain process control strategies, including SOPs and compliance with regulatory standards. Analyze process data to identify trends and opportunities for continuous improvement. Support the selection and qualification of manufacturing equipment and tooling. Lead investigations into underlying causes and implement risk management approaches. Prepare and deliver detailed technical reports and presentations. Recommend and implement data-driven solutions and automation strategies. Apply Lean Manufacturing and Six Sigma methodologies for process flow optimization and cost reduction. Requirements Bachelor's degree in chemical engineering, Manufacturing Engineering, Mechanical Engineering, or related field. Minimum of 4+ years of experience in a chemical, pharmaceutical, or regulated manufacturing environment. Demonstrated ability to encourage and inspire change, promoting positive relationships with teams and partners. Proficiency in statistical analysis tools and data-driven decision-making. Proficient knowledge of Lean Manufacturing principles and Six Sigma methodologies. Strong analytical and problem-solving skills. Excellent verbal and written communication skills. Proven ability to thrive in a collaborative, team-oriented environment. Environmental Conditions Loud Noises (Equipment/Machinery), Office, some degree of PPE required (safety glasses, gowning, gloves, lab coat, earplugs, etc.), Various outside weather conditions, Warehouse

We are seeking a detail-oriented and collaborative Manufacturing Engineer to support both New Product Introduction (NPI) and existing product lines. This role will serve as a critical link between engineering, operations, and customers to ensure manufacturing processes are efficient, cost-effective, and aligned with quality standards. The ideal candidate will be proactive in driving continuous improvement, maintaining documentation, and fostering strong cross-functional relationships. This position requires a strong focus on Design for Manufacturability (DFM), acting as a key liaison between customers and internal teams to ensure that product designs are optimized for production capabilities and cost efficiency. Responsibilities * Collaborate with customers during design and development phases to review part designs and provide DFM feedback that enhances manufacturability, reduces cost, and improves production efficiency. * Lead DFM review sessions with customers and internal stakeholders to identify and address potential design or process issues early in the development cycle. * Act as the primary liaison between customers and internal departments (Engineering, Quality, Operations, CNC Applications), ensuring clear communication and timely resolution of technical issues. * Coordinate internal engineering activities to align with customer requirements, project timelines, and production readiness. * Manage Engineering Change Notices (ECNs) through VMFG and ensure timely updates to control plans, digital attachments, and related documentation. * Communicate with customers regarding prints, specifications, and process clarifications to ensure alignment and manufacturability. * Oversee project and part timelines, track current work status, estimate completion dates, and provide regular updates to management on project status, risks, and performance metrics. * Partner with the Quality Department to address nonconforming products and update control plans as needed. * Research and recommend new manufacturing technologies and process improvements to enhance productivity, product quality, and operational efficiency. * Drive continuous improvement initiatives focused on reducing cycle time, setup time, and production costs, while improving work holding and lead times for first article inspections. * Ensure smooth handoff between Engineering and Operations, confirming parts are production-ready and running correctly. * Maintain a clean, organized, and professional work environment, and lead by example in adhering to all company policies and procedures. Essential Skills * Proficiency in SolidWorks and CAD software. * Strong understanding of Design for Manufacturability (DFM) principles, control plans, and ECN processes. * Experience with ERP/MRP systems (VMFG experience preferred). * Excellent communication and interpersonal skills, with the ability to interface effectively with customers and cross-functional teams. * Demonstrated ability to lead cross-functional teams and drive process improvements. * Familiarity with CNC machining and quality assurance processes. Additional Skills & Qualifications * Bachelor's degree in Manufacturing Engineering, Mechanical Engineering, or a related field. * 3+ years of experience in a manufacturing or industrial engineering role. * Mechanical design and tooling experience. * Knowledge of GD&T, Lean manufacturing, Six Sigma, and sheet metal processes. Job Type & Location This is a Permanent position based out of Elmwood Park, NJ. Pay and Benefits The pay range for this position is $90000.00 - $130000.00/yr. health vision dental 401k (3% company match) Workplace Type This is a fully onsite position in Elmwood Park,NJ. Application Deadline This position is anticipated to close on Jan 19, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Teijin Automotive Technologies is the world leader in the compounding and manufacturing of lightweight composite components for the transportation industries. As an innovative, full-service Tier One supplier, we offer an entrepreneurial environment where you're only limited by your own imagination. In addition to our team-focused environment, we provide industry leading benefits. Called BENEfits4U, our comprehensive offering includes: affordable medical, dental, and vision care; flexible spending accounts; life insurance; 401k with company match and much, much more. Job Description We are seeking a Paint Process Engineer for our Huntington, Indiana Plant. Summary: Responsible for specifying, designing, and implementing robot path programming and paint application. Main Duties and Responsibilities: • Improve the design and process control of the paint department operations. • Equipment and control panel upgrades. • Conveyor control integration with paint robots. • Data acquisition improvements for production reporting. • Safety device and logic changes for zoned safety. • Networking and communications upgrades for reliability. • Allen Bradley PLC logic improvements for uptime and throughput increase. • Specify, design, implement, and track the improvement of robot path programming and optimization of manipulator, applicator, and fluid delivery process. • Equipment specification and procurement, including acting as liaison to builders, customers, and production for paint process and fluid delivery process. • Coordination of trial runs and quality improvement for the paint process. • Implement cost-reduction improvements for both new and existing equipment/processes. • Technical support to all Production and Engineering operations for improvement programs. Qualifications: • Bachelor of Science Degree in Engineering or related field or equivalent experience. • Minimum five years of experience in controls engineering. • Working knowledge of paint department processes and principles. • General knowledge of production control / scheduling systems. • Good analytical / problem-solving skills. • Working knowledge of statistical analysis. • General MS-Office skills, Excel and Access. • Fanuc P-250 experience required. • Able to manage multiple projects and priorities. • Good written and verbal communication skills. • Knowledge of ISO14001 and TS16949 requirements. • Good organizational and time management skills. • Working knowledge of lean manufacturing principles. • Strong knowledge of PLC programming and networking. • Strong knowledge of paint application process. • Basic knowledge of machining / tooling; and electrical / schematics If you enjoy innovation, and an opportunity to learn and contribute to a growing organization, Teijin Automotive Technologies is the place for you!

Company profile: POLYVANTIS is a global, multi-material player with some of the most coveted and iconic brands in the industry - such as PLEXIGLAS , ACRYLITE and LEXAN™ Film and Sheet. With 1,500 employees and 15 production sites worldwide, we offer unmatched global capabilities, providing customers with innovative solutions in sheet and film for air and rail, automotive, building and construction, electrical, healthcare and security, and lighting and signage markets. A career at POLYVANTIS means you will make an impact on the Company's success each day. We offer excellent pay and benefits, along with comprehensive learning programs to help grow your career. Apply now to join our team and we will become Stronger Together. Job Purpose We are seeking a data-driven Process Engineer with a strong background in Six Sigma methodologies and continuous improvement to join our Mt. Vernon team. This role will be pivotal in optimizing manufacturing processes, improving product quality, increasing throughput, and driving operational excellence in our sheet and film production lines. Primary Responsibilities Lead process improvement initiatives using Six Sigma, Lean, and data analysis tools to reduce waste, improve yield, and enhance product quality. Analyze production data to identify trends, bottlenecks, and opportunities for improvement. Collaborate with production, quality, and maintenance teams to develop and implement process controls and best practices. Lead root cause analysis (RCA) efforts and implement corrective/preventive actions (CAPA). Drive standardization of processes and documentation, including process maps, work instructions, and control plans. Support the commissioning and scale-up of new equipment, materials, or processes. Monitor key process indicators (KPIs) and report on process performance and improvement progress. Train operations staff on new procedures and quality initiatives. Partner with corporate engineering, R&D, and safety to ensure alignment with organizational goals. Provide sustainable opportunities for improvement Requirements: Bachelor's degree in Chemical Engineering, Mechanical Engineering, Materials Science, or a related field. 3-7 years of experience in manufacturing or process engineering, preferably in film, sheet extrusion, or plastics. Strong experience in Six Sigma (Green Belt or Black Belt preferred) and statistical process control (SPC). Proficiency with data analysis tools (e.g., Minitab, JMP, Excel, Power BI). Demonstrated ability to drive change and lead cross-functional projects. Excellent problem-solving, communication, and project management skills. Hands-on, plant-floor orientation with a commitment to safety and operational excellence. Why Join Polyvantis Make a measurable impact in a high-visibility role at a growing site. Join a collaborative culture that values curiosity, integrity, and action. Gain exposure to a diverse product portfolio and advanced manufacturing technologies. Enjoy opportunities for career growth within a global company committed to innovation and sustainability. Work Availability Regular, predictable attendance is an essential function of this position. Applicants must be regularly available and willing to work Monday- Friday during assigned hours of operation and such other hours as the company determines are necessary or desirable to meet business needs. We are proud to be a diverse and an equal opportunity employer. We are fully committed to a culture of respect and inclusion.

We are looking for a Process Engineer for our Westbury, NY facility. In this role you will be the subject matter expert of the products and manufacturing processes within the Westbury Materials Operations Team. The Process Engineer supports day-to-day powder manufacturing operations, leads continuous improvement & CAPEX projects, maintains proper documentation of Manufacturing process plans (MPP) & manages SAP BOM/Recipes for the products. Your Responsibilities: * Serving as a technical resource for Production personnel. * Sustaining/improving product quality. * Supporting and managing scaleup and process improvement projects of various sizes. * Identifying and executing continuous improvement projects (yield improvements, cost savings initiatives, cycle time reductions, etc.). * Identifying and validating new equipment to optimize/improve manufacturing processes. * Supporting various capital expenditure projects. * Leading root cause investigations. * Addressing nonconformances promptly. * Implementing corrective and preventive actions. * Maintaining SAP master data (BOMs, recipes, etc.). * Working closely with the Controller on product costing and other financial analyses. * Transferring products and new technologies from R&D to Production (scale up). * Creating, updating, and providing training on work instructions, manufacturing batch records, and other documentation. Your Profile: * Bachelor's degree in chemical, mechanical or materials engineering with preferably 1-2 years of manufacturing experience in a chemical or pharmaceutical environment, experience particularly involving the handling or production of materials in powder form will be a plus. * Material engineering & processing knowledge. * Excellent analytical and problem-solving skills. * Ability to read & analyze large scale data. * Extensive experience using various root cause analysis tools/techniques. * Experience managing projects and leading cross-functional teams. * Ability to communicate effectively with people in various departments across all levels of the organization, including production personnel and senior management. * Knowledge of powder manufacturing and thermal spray processes, preferred. * Knowledge of mechanical engineering principles, and maintenance and facilities activities, preferred. * Knowledge of lean and six sigma methodologies, preferred. * Proficiency in SAP is preferred. * Proficiency in Microsoft Excel, Word, and PowerPoint is required. Working knowledge of Microsoft Visio, Project, and Access, as well as AutoCAD, is preferred. We offer: Aside from a dynamic global culture and leading market position, we are proud to offer our employees development opportunities, competitive salary and a robust benefit program ALL available on first day of employment! The perks and benefits of working at Oerlikon include the following: * Comprehensive medical and prescription drug plan with low premiums, company sponsored HSA contributions and without cumbersome waiting periods to keep you going strong. * Excellent Dental and Vision coverage. * Employee Assistance, Financial and Wellness programs to help improve all aspects of your life journey. * 401(k) retirement savings plan with significant company match and financial planning and education options to help you achieve your retirement goals * Tuition reimbursement and internal education resources to satisfy your love of learning so you can continue to grow with us! * Generous paid time off to support your physical and mental wellbeing. * 12 paid company holidays to occasionally extend your weekends or time off. * 100% company paid life insurance and disability insurance * Employee Referral Bonus program because why not to bring your friends to work everyday! Why Oerlikon: Diversity is not merely a result of our presence in more than 30 countries and 170 locations worldwide. It's a reflection of who we are - we are proud to have more than 11.000 employees representing over 80 nationalities working for Oerlikon. We strive to create a more appealing place to work for diverse groups, regardless of background, language, beliefs or gender. We take our ESG responsibilities seriously, setting tough targets for ourselves as we work towards ensuring we meet our sustainability responsibilities. #joinoerlikonus #joinourteam Are you curious? Then release your passion to succeed and

Linde Advanced Material Technologies Inc. Manufacturing Engineer Orangeburg, NY, United States | req26836 What you will enjoy doing* * In this role you will analyze current manufacturing processes and identify areas for improvement in efficiency, quality, and cost * You will design, implement, and refine production workflows, tooling, and fixtures to support lean manufacturing principles * Collaborate with cross-functional teams including production, quality, and maintenance to troubleshoot and resolve process issues * You will develop and maintain documentation for manufacturing procedures, work instructions, and equipment specifications * Support the integration and programming of CNC machines and metal fabrication equipment and recommend new technologies or equipment to enhance manufacturing capabilities * Recommend process and operational changes to overcome process issues, avoid deviations, and improve productivity by analyzing and interpreting data from manufacturing operations * Ensure compliance with safety standards and regulatory requirements in all engineering activities What makes you great * You will possess a bachelor's degree in mechanical engineering or related field * 3+ years of experience in a manufacturing engineering role, and in a metalworking environment preferred * You should have an understanding of the properties, behavior, and selection of materials to choose the best option for a specific application's stress, temperature, and environment * You have strong project management abilities, experience in planning, scheduling, budgeting, and coordinating resources to bring projects from concept through to completion * You are required to have strong technical skills and have the ability to work across all levels in the organization * Experience with C/C++ for embedded systems development and real-time control of mechanical hardware preferred Why you will love working with us Linde Advanced Material Technologies, formerly Praxair Surface Technologies, is a company that revolutionizes industries through innovative materials and surface coatings. We are leaders in advanced materials and offer metal powders, sputtering targets, and surface coatings that enhance performance across various sectors. Our strong focus on innovation is evident in our superior technologies for the aerospace, energy, semiconductor, automotive, and industrial industries. Linde employees learn and abide the Linde Code of Ethics and Code of Conduct by demonstrating honesty, integrity, professionalism in all communications, actions, and decisions. What we offer you! At Linde, the sky is not the limit. If you're looking to build a career where your work reaches beyond your job description and betters the people with whom you work, the communities we serve, and the world in which we all live, at Linde, your opportunities are limitless. Be Linde. Be Limitless. Linde offers competitive compensation and an outstanding benefits package. Enjoy access to health, dental, disability, and life insurance, paid holidays and vacation, 401(k) matching, pension benefits, an employee discount program, and opportunities for educational and professional growth. Additional compensation may vary depending on the position and organizational level. Build your future with us while making an impact every day! The salary range for this role is $81,600-$112,200. Have we inspired you? Let´s talk about it We are looking forward to receiving your complete application. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, protected veteran status, pregnancy, sexual orientation, gender identity or expression, or any other reason prohibited by applicable law. Linde Advanced Material Technologies Inc. acts responsibly towards its shareholders, business partners, employees, society and the environment in every one of its business areas, regions and locations across the globe. The company is committed to technologies and products that unite the goals of customer value and sustainable development. * The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Therefore employees assigned may be required to perform additional job tasks required by the manager. #LI-AD1

Job Description Description/Comment: ****HYBRID**** Hours: 8:00am to 5:00pm This function will be directly supporting the EUMDR project on Site. Requirements: Education and Special Training Required: Bachelors Degree in Engineering or relevant field of study Qualifications and Work Experience Required 1-3 years experience in a production/manufacturing environment. Demonstrated computer skills using Microsoft Office applications (Word, Excel, PowerPoint, Project, etc), and experienced work in a Quality Management System and UDI/MDD/MDR/UKCA Regulatory Compliance project experience is preferred. Demonstrated interpersonal, communication and presentation skills. Must be comfortable presenting at team level meetings and lead meetings as necessary. Demonstrate strong teamwork and time management skills as well as be able to operate in a fast-paced environment. Ability to perform in and be challenged by a multi-disciplinary team-based environment, which places a high degree of emphasis on accountability for quality/GMP/GDP compliance. Provide technical support for quality control, process improvement, equipment qualifications, and process validations. Operate within s quality management system (QMS) to produce and/or review documentation such as, inspection guide sheets, product drawings, dynamic control plans (DCPs), and standard operating procedures (SOPs) Additional Job Details: Periodically work independently with vendors. 2D drawing & GD&T knowledge or experience. Create and manage Engineering Change Requests as well as product impact assessments. Manage Engineering Change Notices for process changes from creation to final approval Demonstrate a general understanding of Product Part Approval Process (PPAP) Demonstrate a general understanding of First Article Inspection (FAI) process Periodically lead projects and processes; work with cross-functional teams to get these projects completed. Ability to multi-task between different projects and changes. Investigate Quality issues for root cause and recommend/implement corrective actions. Ability to oversee team members workload and provide support when issues arise. Work to support team members as both mentor/mentee when necessary.

Crestron Electronics, Inc. has an opportunity for an experienced Sr. Process Engineer to join a dynamic team to support our PC board assembly operation in Orangeburg, NY. This role requires an in-depth understanding of electronic circuit board assembly and design for manufacturing analysis. The candidate will utilize the latest CAD tools to analyze new board designs and collaborate with the development teams to verify design guidelines are met to ensure ease of manufacturing, reliability, and high yields. You will work on projects to document new circuit board assembly procedures and participate in day-to-day resolution of PCB board production issues at our plant. This includes creation of high-level work instructions, programming specialized assembly equipment, and assisting in the training of production personnel and operators. As Sr. Process Engineer you will initiate lean initiatives by identifying key areas for improvement and drive improvement projects with stakeholders and cross functional teams. Responsibilities: Provide technical support to the PC board production operation. Create and maintain process documents related to PCB assembly processes and equipment. Manage engineering design updates and communicate changes through proper documentation. Perform IPC-A-610 based Valor DFM analysis on new circuit board designs, and document feedback to the design team. Utilize CAD-based tools to analyze design or component issues to eliminate PCB assembly problems. Develop and maintain assembly aids and production fixtures using 3D/2D CAD software. Initialize engineering change requests to improve product assembly, quality, and cost. Programming of specialized process equipment to support PCB production. Engage with the production teams to identify and eliminate process bottlenecks. Work closely with QC to identify and resolve materials and vendor-related issues. Participate in analyzing performance metrics to help improve process yields and prevent down time Work with equipment manufacturers to identify and select new equipment and methods. Participate in continuous improvement and lean manufacturing initiatives and practices. Utilize MS Power Platform to automate business processes and improve manufacturing efficiencies. Other duties as assigned. Qualifications: BS in Mechanical Engineering or other closely related field. 8+ years of experience in the electronics industry with a focus on circuit board DFM and assembly. Experience utilizing 3D CAD systems (Creo, Solid works, or other) to design functional parts and create technical drawings. Have working knowledge of IPC-A-610 industry standards for electronic assemblies. Experienced using Valor DFM application or suitable alternatives Experienced using Microsoft Power Platform to automate business processes and analyze data. Experienced with Lean Six Sigma practices. Knowledge of Microsoft Office. Proven problem solver with technical decision-making skills. Excellent oral and written communication skills. The ability to work in a collaborative team environment is necessary. Ability to adapt and learn in a challenging environment. Ability to work independently without continuous supervision. Mechanically inclined with a drive for process improvement.

Engineer, Manufacturing Division: Operations Department: Manufacturing Reports to: COO About Us: Quantum Computing Inc. (QCi) (Nasdaq: QUBT) is an innovative, integrated photonics company that provides accessible and affordable quantum machines to the world today. QCi products are designed to operate at room temperature and low power at an affordable cost. The Company's portfolio of core technology and products offer unique capabilities in the areas of high-performance computing, artificial intelligence, cyber security as well as remote sensing applications. Job Overview: We are seeking a dedicated and passionate Manufacturing Engineer to build our production team in Hoboken, NJ. In this vital role, you will define process methodology from engineering to pilot manufacturing, create assembly drawings, and test protocols for manufacturing and assembling cutting-edge products. You will conduct thorough testing to ensure they meet quality standards and specifications, playing a key role in our quality control processes. Collaborating with cross-functional teams of electrical, FPGA, optical, mechanical, embedded, and software engineers, you will enhance product performance, troubleshoot challenges, and drive continuous improvement initiatives in our products. This is a unique opportunity to build a team to help define the manufacturing process from scratch, in a low volume, highly technical environment. Duties and Responsibilities: * Develop and execute innovative test plans and procedures to validate product performance and reliability. * Supervising the assembly of electronic, optical, and mechanical components with precision and care, adhering to specifications and engineering drawings. * Conduct insightful root cause analyses on test failures, document them properly, and implement corrective actions. * Collaborate with design teams to refine assembly processes and test methodologies. * Develop, document and maintain detailed test results, assembly processes, and technical documentation. * Provide valuable feedback to design teams regarding product design and quality improvements. * Develop relationships and maintain vendor ecosystem in support of low volume production. * Uphold manufacturing, safety standards, and regulations throughout all assembly and testing processes. * Implement quality control measures to assess and guarantee product quality throughout the assembly and testing phases. * Maintain and organize tools and equipment to ensure a safe and clean work environment. * Guide and direct efforts of Manufacturing Technicians. Required Skills and Experience: * Bachelor's degree or Masters degree in Electrical Engineering, Mechanical Engineering, or a related field. * 4 or more years of experience in product assembly and testing, preferably in a dynamic manufacturing environment (Engineering to Pilot Manufacturing). * Experience in process definition, creation of supporting documentation such as Test, Assembly, Quality Etc.. * Familiarity with quality assurance standards and manufacturing methodologies, such as ISO, Six Sigma, Lean, etc.. * Strong understanding of electronic components, assembly techniques, and testing procedures. * Proficiency in using test equipment and tools, including experience with lab instruments such as DMMs, oscilloscopes, logic analyzers, and spectrum analyzers. * Familiarity with PLM and ERP systems. * Dexterity in the use of hand tools, electronics soldering, and board reworking. * Basic programming skills. Able to code in C, C++, MATLAB/Octave, or Python. * Able to lift weights to OSHA limit (50 lbs.) when required (occasionally). * Excellent problem-solving skills, open-minded, and a keen attention to detail. * Ability to work collaboratively in a supportive, team-oriented environment. * Strong communication skills, both written and verbal. Additional Preferred Skills: * Experience with automated testing equipment and techniques. * Basic knowledge of Mechanical CAD software * Ability to read and write electronic circuit diagrams. * Exposure to project management tools and techniques.

Engineer, Manufacturing Division: Operations Department: Manufacturing Reports to: COO About Us: Quantum Computing Inc. (QCi) (Nasdaq: QUBT) is an innovative, integrated photonics company that provides accessible and affordable quantum machines to the world today. QCi products are designed to operate at room temperature and low power at an affordable cost. The Company's portfolio of core technology and products offer unique capabilities in the areas of high-performance computing, artificial intelligence, cyber security as well as remote sensing applications. Job Overview: We are seeking a dedicated and passionate Manufacturing Engineer to build our production team in Hoboken, NJ. In this vital role, you will define process methodology from engineering to pilot manufacturing, create assembly drawings, and test protocols for manufacturing and assembling cutting-edge products. You will conduct thorough testing to ensure they meet quality standards and specifications, playing a key role in our quality control processes. Collaborating with cross-functional teams of electrical, FPGA, optical, mechanical, embedded, and software engineers, you will enhance product performance, troubleshoot challenges, and drive continuous improvement initiatives in our products. This is a unique opportunity to build a team to help define the manufacturing process from scratch, in a low volume, highly technical environment. Duties and Responsibilities: Develop and execute innovative test plans and procedures to validate product performance and reliability. Supervising the assembly of electronic, optical, and mechanical components with precision and care, adhering to specifications and engineering drawings. Conduct insightful root cause analyses on test failures, document them properly, and implement corrective actions. Collaborate with design teams to refine assembly processes and test methodologies. Develop, document and maintain detailed test results, assembly processes, and technical documentation. Provide valuable feedback to design teams regarding product design and quality improvements. Develop relationships and maintain vendor ecosystem in support of low volume production. Uphold manufacturing, safety standards, and regulations throughout all assembly and testing processes. Implement quality control measures to assess and guarantee product quality throughout the assembly and testing phases. Maintain and organize tools and equipment to ensure a safe and clean work environment. Guide and direct efforts of Manufacturing Technicians. Required Skills and Experience: Bachelor's degree or Masters degree in Electrical Engineering, Mechanical Engineering, or a related field. 4 or more years of experience in product assembly and testing, preferably in a dynamic manufacturing environment (Engineering to Pilot Manufacturing). Experience in process definition, creation of supporting documentation such as Test, Assembly, Quality Etc.. Familiarity with quality assurance standards and manufacturing methodologies, such as ISO, Six Sigma, Lean, etc.. Strong understanding of electronic components, assembly techniques, and testing procedures. Proficiency in using test equipment and tools, including experience with lab instruments such as DMMs, oscilloscopes, logic analyzers, and spectrum analyzers. Familiarity with PLM and ERP systems. Dexterity in the use of hand tools, electronics soldering, and board reworking. Basic programming skills. Able to code in C, C++, MATLAB/Octave, or Python. Able to lift weights to OSHA limit (50 lbs.) when required (occasionally). Excellent problem-solving skills, open-minded, and a keen attention to detail. Ability to work collaboratively in a supportive, team-oriented environment. Strong communication skills, both written and verbal. Additional Preferred Skills: Experience with automated testing equipment and techniques. Basic knowledge of Mechanical CAD software Ability to read and write electronic circuit diagrams. Exposure to project management tools and techniques.

Introduction ASML US brings together the most creative minds in science and technology to develop lithography machines that are key to producing faster, cheaper, more energy-efficient microchips. We design, develop, integrate, market and service these advanced machines, which enable our customers-the world's leading chipmakers-to reduce the size and increase the functionality of their microchips, which in turn leads to smaller, more powerful consumer electronics. Our headquarters are in Veldhoven, the Netherlands, and we have 18 office locations across the United States, including Chandler, AZ; San Jose and San Diego, CA; Wilton, CT; and Hillsboro, OR. Your Assignment: As a Process Engineering Intern in Wilton, CT, you will work alongside our bonding/contacting and photolithography/wet etch teams to support optical manufacturing processes. You will gain hands-on experience in process optimization and problem-solving while supporting critical optical manufacturing processes. Key Responsibilities: Optimize production processes involving bonding and contacting of glass substrates, wet etching, and photolithography. Design and execute experiments to identify root causes of production issues. Analyze data statistically to troubleshoot and validate process improvements. Investigate process deficiencies and recommend enhancements to improve control and reliability. Develop robust documentation, including work instructions for manufacturable processes. Your Profile Currently pursing a Bachelor's degree in one of the following fields: Chemistry Chemical Engineering Industrial Engineering Materials Science Optical Engineering Physics Skills: To thrive in this job, you'll need: Ability to learn and apply new information quickly. Strong data interpretation and analytical skills. Attention to detail with a high degree of accuracy. Proven ability to perform effectively in a dynamic environment with changing priorities. Results-driven mindset with ownership and accountability. Ability to identify bottlenecks and drive improvements. Strong communication skills-clear, concise, and professional. Ability to work independently and collaboratively with minimal supervision. Commitment to customer satisfaction through quality and efficiency. Ability to follow strict procedures and meet timelines. Work Environment & Physical RequirementsOffice Setting: Routine activities include sitting, walking, talking, hearing, and using hands for keyboarding and handling. Occasional movement around campus and lifting/moving up to 20 lbs. Vision requirements: close vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Factory Setting (Cleanroom): Must be willing to work in a cleanroom environment under ISO 9000/14000 standards, wearing full gowning (coveralls, hood, safety shoes, face mask, nitrile gloves, and safety glasses). Work around overhead cranes, fork trucks, motorized pallet movers, lasers, ladders, platforms, and chemicals. Occasional lifting/moving up to 20 lbs. Moderate temperature and noise levels Reasonable accommodations will be provided for individuals with disabilities. Additional Responsibilities: There is potential for exposure to strong magnetic fields, high voltage and currents. This position requires access to controlled technology, as defined in the United States Export Administration Regulations (15 C.F.R. § 730, et seq.). Qualified candidates must be legally authorized to access such controlled technology prior to beginning work. Business demands may require ASML to proceed with candidates who are immediately eligible to access controlled technology. Inclusion and diversity ASML is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, veteran status, disability, sexual orientation, or gender identity. We recognize that inclusion and diversity is a driving force in the success of our company. Need to know more about applying for a job at ASML? Read our frequently asked questions. Request an Accommodation ASML provides reasonable accommodations to applicants for ASML employment and ASML employees with disabilities. An accommodation is a change in work rules, facilities, or conditions which enable an individual with a disability to apply for a job, perform the essential functions of a job, and/or enjoy equal access to the benefits and privileges of employment. If you are in need of an accommodation to complete an application, participate in an interview, or otherwise participate in the employee pre-selection process, please send an email to USHR_Accommodation@asml.com to initiate the company's reasonable accommodation process. Please note: This email address is solely intended to provide a method for applicants to initiate ASML's process to request accommodation(s). Any recruitment questions should be directed to the designated Talent Acquisition member for the position.

Northern Architectural Systems ("NAS") is a growth-minded, locally owned and operated company which is dedicated to servicing our customers. We offer high quality, energy-efficient fenestration and building facade solutions to meet the requirements of a demanding market, while remaining environmentally-friendly. Northern Architectural Systems has been recognized by INC Magazine on the list of the top 5000 Fastest Growing Private Companies in America and as one of the top 50 Fastest Growing Companies in New Jersey by NJBIZ Magazine. Overview: We are looking to fulfill our need for a Manufacturing Engineer at our Teterboro, NJ facility. This role will be responsible for assisting our production staff with product design, fabrication, assembly, tooling and materials as well as assisting with scheduling, planning and forecasting. This individual will be accountable for assuring project accuracy and quality from conception to completion. The Manufacturing Engineer must possess exceptional organizational, problem-solving, and communication skills while being results-driven with a keen attention to detail.

Unilever is one of the world's leading suppliers of Food, Refreshments, Health & Wellness, and Home & Personal Care products with sales in more than 190 countries. In the United States, some of our iconic brands are: Axe, Degree, Dove, Dove Men+Care, Hellmann's, Nexxus, Shea Moisture, TRESemmé, and Vaseline. All the preceding brand names are trademarks or registered trademarks of the Unilever Group of Companies. We are a purpose-led and future-fit organization developing our products for peoples' lives today and for the changing environment tomorrow, aiming to make sustainable living commonplace. Unilever offers vast and exciting career paths within R&D. Creating new innovations, delivering consumer benefits, and enhancing our brands as a force for good - it's all yours in Unilever R&D. As a process development summer intern at Unilever, you will learn how we develop and commercialize new personal care formulations in either the skin care, skin cleansing, hair care, or deodorant teams. You will scale up and deploy the latest technologies, deliver breakthrough cosmetic and health benefits, and bring innovations to life for our consumers. What You'll Do With guidance from a manager and team of functional experts, summer interns will manage one major summer project on their own in a process engineering role. This project will address a major technical challenge and opportunity for one of Unilever's well-known hair, skin cleansing, or skin care brands. Interns will carry out the project within a brand formulation team, processing specialists, or within an R&D support function. Possible project topics include: + Scaling up breakthrough technologies in a major consumer product, addressing feasibility constraints in our manufacturing assets while maintaining critical product attributes like sensory and cost. + Resolving manufacturing quality issues in some of the largest consumer products in the world by studying both processing and formulation variables. + Modeling processing data at both the pilot and factory scale to drive product enhancement and cost savings. In any project, interns will learn chemical processing principles and product measurement methods unique to formulated consumer products (such as low temperature processing, rheology analysis, and emulsification). You will also apply statistical experimental design and modeling tools to specific needs of the overall Unilever business. The work will be primarily on-site and involve extensive hands-on work in the laboratory or pilot-plant facilities. Interns can expect to run pilot-scale batches of formulations systematically varying processing variables, chemical factors, or ingredients. They will perform their own characterization using rheology measurements and other industry-standard measurements. Interns will plan experiments, analyze their data using statistical and graphical tools, and generate predictive models. They will generate input and incorporate feedback from a cultivated network of technical experts within Unilever to enhance the delivery of their project. Who You Are You're a born leader: You will lead your own project You're a dot connector: You will solicit the input of technical experts, apply digital tools to the design of experiments, generate insights from your data, and provide recommendations that meet business objectives You're a storyteller: You will present your project to senior management You're a culture & change champion: You bring your own experiences and uniqueness to the team, which is valued in our inclusive work environment What You'll Need to Succeed + Undergraduate with sophomore or junior status based on Major in Chemical Engineering or other related major + Proficiency in Microsoft Office suite (Word, Excel, PowerPoint) + Proven willingness and ability to learn new technical skills + Minimum GPA of 3.0 on a 4.0 scale + Ability to conduct an experimental program to generate relevant, high-quality data with subsequent data analysis and interpretation + Ability to work under pressure in a fast-paced environment in order to meet project deadlines + Ability to work with others, communicate effectively, and contribute to cross-functional teams + Willingness to relocate to the Trumbull, CT area for the duration of the internship. Next Steps Life at Unilever is a lot of fun - just like our application process! Check out what you'll experience when you apply for one of our internships or co-ops: Application - Start by completing our simple online application. You can import your details from your LinkedIn profile to speed up the process. You can only apply to one function, so carefully consider which role you would like to pursue before applying. Assessment - After your application, if you meet the basic requirements, we'll invite you to participate in a series of fun games that looks at different cognitive, emotional, and social traits. This will help us find the best fit for you and you will receive personalized feedback after completing the games. Digital Interview - Upon successful completion of the assessment, you will be invited to participate in a digital interview where you can solve real-world problems using Unilever scenarios. This will give you insight into our company culture and how we do business. The interview is split into two parts: three short hypothetical questions followed by a business case. You can record and complete your video anytime, anywhere. All you need is a computer or mobile device with access to video recording (usually standard in most devices) and a stable internet connection. Discovery Center - Once the interview is complete, we'll invite our top matches to our offices in the Greater New York City or Toronto areas (depending on which job you applied for) for a truly immersive experience. You'll get to experience a number of exciting activities and projects along with your peers, meet our leaders, and receive personalized coaching and feedback. The exercises are designed around a real business case study, enabling us to tap into your potential while giving you further insight into what it's really like to work at Unilever. What We Can Offer You | Top Notch Employee Health & Well Being Benefits (****************************************************************** | Every Voice Matters (******************************************************************************************************************************************* | Global Reach (********************************* | Life at Unilever (************************************************* | Careers with Purpose (********************************************************************* | World Class Career Development Programs (************************************************* | Check Out Our Space (************************************************** | Focus On Sustainability (********************************************************************* To receive communication about your application, please add ******************** to your safe senders list, and ensure your mobile phone number is correctly entered in your application. Unilever is an organization committed to diversity and inclusion to drive our business results and create a better future every day for our diverse employees, global consumers, partners, and communities. We believe a diverse workforce allows us to match our growth ambitions and drive inclusion across the business. Equal Opportunity/Affirmative Action Employer Minorities/Females/Protected Veterans/Persons with Disabilities Applicants and employees are protected from discrimination under Federal law. For more information, please see EEO is the Law Employment is subject to verification of pre-screening tests, which may include drug screening, background check, credit check and DMV check. If you are an individual with a disability in need of assistance at any time during our recruitment process, please contact us at ************** or NAAccommodations@unliever.com . Please note: These lines are reserved for individuals with disabilities in need of assistance and are not a means of inquiry about positions or application statuses. ------------------------------------ At Unilever, inclusion is at the heart of everything we do. We welcome applicants from all walks of life and are committed to creating an environment where everyone can thrive/succeed. All applicants will receive fair and respectful consideration, and we actively support the growth and development of every employee.Unilever is an Equal Opportunity Employer/Protected Veterans/Persons with Disabilities.For more information on your federal rights, please see Know Your Rights: Workplace Discrimination is Illegal (************************************************************************************************** Employment is subject to verification of pre-screening tests, which may include drug screening, background check, credit check and DMV check. If you are an individual with a disability in need of assistance at any time during our recruitment process, please contact us at NA.Accommodations@unilever.com. Please note: This email is reserved for individuals with disabilities in need of assistance and is not a means of inquiry about positions or application statuses. The Protected Veterans or Individuals with Disabilities AAP narratives are available for inspection by any employee or applicant for employment Monday through Friday during normal business hours at establishment. Job Category: Research & Development Job Category: Early Careers Job Type: Full time Industry:

Job Title: Senior Quality EngineerJob Description The Senior Quality Engineer is responsible for leading quality assurance initiatives, ensuring that processes, products, and systems comply with regulatory and company standards. This position serves as a technical resource for cross-functional teams, focusing on complaint handling, non-conformance reports (NCRs), root cause analysis, and leading audits. Responsibilities * Perform quality activities in support of operations, contract manufacturers, and R&D. * Support design and engineering change processes and associated documentation. * Support internal and external audit activities and work to resolve audit nonconformities. * Lead quality activities related to Corrective and Preventive Action (CAPA) processes. * Represent Quality Engineering in the development and maintenance of process and product risk assessments. * Participate in Material Review Board reviews, including material segregation, investigation, corrections, and dispositions. * Design and implement robust quality controls for new and existing processes. * Develop and maintain risk management documentation in alignment with ISO standards. * Oversee process validation activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols and reports. * Act as a liaison with regulatory bodies during audits and inspections. * Monitor and report quality metrics, driving continuous improvement initiatives. Essential Skills * Quality engineering * Quality assurance * CAPA * ISO standards * Medical device industry experience * Quality control * Root cause analysis * Complaint handling * NCRs * Process Validation * Quality management system * Inspection Additional Skills & Qualifications * Bachelor's Degree in an Engineering discipline, preferably Biomedical, Mechanical or Industrial. * Minimum of 5+ years of experience in Quality Engineering. * Experience with Risk Management, preferably ISO standards. * Experience with quality audits required. * Previous medical device industry experience. * Experience with complaint handling, CAPAs, and NCRs required. Work Environment This is a full-time, 12-month contract position with a medical device manufacturer located in Orangeburg, NY. The role operates within a team of 23, from 8:30 AM to 4:00 PM. The work setting is a medical device environment, where you will be the sole Quality Engineer onsite in NY. The Senior Quality Manager is based in Buffalo, NY, with other Quality Engineers in Westboro, MA. The position offers 1 week of accrued vacation time, accrued sick time, and 6 paid holidays. Job Type & Location This is a Contract position based out of Orangeburg, NY. Pay and Benefits The pay range for this position is $40.87 - $48.08/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Orangeburg,NY. Application Deadline This position is anticipated to close on Jan 31, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Description Northern Architectural Systems (“NAS”) is a growth-minded, locally owned and operated company which is dedicated to servicing our customers. We offer high quality, energy-efficient fenestration and building facade solutions to meet the requirements of a demanding market, while remaining environmentally-friendly. Northern Architectural Systems has been recognized by INC Magazine on the list of the top 5000 Fastest Growing Private Companies in America and as one of the top 50 Fastest Growing Companies in New Jersey by NJBIZ Magazine. Overview: We are looking to fulfill our need for a Manufacturing Engineer at our Teterboro, NJ facility. This role will be responsible for assisting our production staff with product design, fabrication, assembly, tooling and materials as well as assisting with scheduling, planning and forecasting. This individual will be accountable for assuring project accuracy and quality from conception to completion. The Manufacturing Engineer must possess exceptional organizational, problem-solving, and communication skills while being results-driven with a keen attention to detail. Requirements Essential Duties and Responsibilities (additional duties may be assigned): Familiar with work orders, shop drawings, pick tickets, routings, schedules, material labels, part drawings and inspection data records. Develop a working knowledge of the capabilities for aluminum, plastics, gaskets, glazing and other materials associated with the business Assist in the design and development of new products Generate a bill of materials (BOM) for the Purchasing and Production departments. Offer suggestions for changes to documentation, specifications, and/or anything related with the BOM, orders and confirmations Participate in group discussions and meetings with management Provide assistance in resolving manufacturing challenges Enter and maintain operational data such as part numbers, batches, sizes and revision levels in NAS's systems. Responsible for developing production documents, managing revisions and communicating changes across various formats and departments. Assist in maintaining folders and records related to order confirmations, material allocation and order production with the factory. Ensure all orders are completed in production, according to all quality and technical specifications. Provide clerical input as required for monthly reporting and scheduling and assist in quarterly forecasting. Minimum Requirements: Associate's Degree in Engineering or Bachelor of Engineering degree Mechanical engineering knowledge a plus 1+ years' experience as a Mechanical or Manufacturing Engineer or similar position Must have basic knowledge of AutoCAD Able to read fabrication drawings and knowledgeable in basic measurement methods Familiarity with manufacturing operations Strong organizational and problem-solving skills Able to work under pressure Ability to plan and prioritize activities Fluency in English, both written and verbal, displaying strong written and oral communications Computer literate and working knowledge of MS Office Benefits Full-time position Salary Range: $60,000 - $70,000 (commensurate with relevant work experience) Medical, Dental and Vision benefits offered 401(k) PTO (Paid Time Off) Employee Training

Job Title: Senior Quality EngineerJob Description The Senior Quality Engineer is responsible for leading quality assurance initiatives, ensuring that processes, products, and systems comply with regulatory and company standards. This position serves as a technical resource for cross-functional teams, focusing on complaint handling, non-conformance reports (NCRs), root cause analysis, and leading audits. Responsibilities + Perform quality activities in support of operations, contract manufacturers, and R&D. + Support design and engineering change processes and associated documentation. + Support internal and external audit activities and work to resolve audit nonconformities. + Lead quality activities related to Corrective and Preventive Action (CAPA) processes. + Represent Quality Engineering in the development and maintenance of process and product risk assessments. + Participate in Material Review Board reviews, including material segregation, investigation, corrections, and dispositions. + Design and implement robust quality controls for new and existing processes. + Develop and maintain risk management documentation in alignment with ISO standards. + Oversee process validation activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols and reports. + Act as a liaison with regulatory bodies during audits and inspections. + Monitor and report quality metrics, driving continuous improvement initiatives. Essential Skills + Quality engineering + Quality assurance + CAPA + ISO standards + Medical device industry experience + Quality control + Root cause analysis + Complaint handling + NCRs + Process Validation + Quality management system + Inspection Additional Skills & Qualifications + Bachelor's Degree in an Engineering discipline, preferably Biomedical, Mechanical or Industrial. + Minimum of 5+ years of experience in Quality Engineering. + Experience with Risk Management, preferably ISO standards. + Experience with quality audits required. + Previous medical device industry experience. + Experience with complaint handling, CAPAs, and NCRs required. Work Environment This is a full-time, 12-month contract position with a medical device manufacturer located in Orangeburg, NY. The role operates within a team of 23, from 8:30 AM to 4:00 PM. The work setting is a medical device environment, where you will be the sole Quality Engineer onsite in NY. The Senior Quality Manager is based in Buffalo, NY, with other Quality Engineers in Westboro, MA. The position offers 1 week of accrued vacation time, accrued sick time, and 6 paid holidays. Job Type & Location This is a Contract position based out of Orangeburg, NY. Pay and Benefits The pay range for this position is $40.87 - $48.08/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Orangeburg,NY. Application Deadline This position is anticipated to close on Jan 31, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.