Industrial engineer jobs in Bayonne, NJ

The ideal candidate possesses both a high level of technical expertise and an innate passion to build. You will play a critical role in creating and refining processes in order to improve manufacturing safety, quality, and productivity. Responsibilities Participate in PPAP process, including drawing feasibility reviews, manufacturing reviews, Failure Modes and Effects Analyses (FMEAs) reviews, etc. Collaborate with other departments to investigate and address quality-related issues using methodologies like 8D, Kaizen, DMAIC, and root cause analysis. Develop and maintain production-related documentation and Standard Operating Procedures (SOPs). Qualifications BS degree in Mechanical Engineering, Manufacturing/Industrial Engineering, or equivalent. 2+ years of engineering experience within a high-volume manufacturing environment. Experience with Continuous Improvements, Lean, Six Sigma, Kaizen, and 5S tools. To all staffing agencies: Wiss does not utilize 3rd party firms for any internal or client positions. Please be advised, Wiss is not responsible for any fees related to unsolicited resumes. All unsolicited resumes will become the property of Wiss.

Job Title: Project Quality Engineer Shift: 1st Shift (Monday - Friday) Pay Rate: Up to $75000-$95,000 annually (commensurate with experience) Type: Direct Hire Reports To: QA Manager Dept.: Quality Assurance Job Description The Project Quality Engineer supports the Quality Assurance Manager in overseeing the Quality Assurance program for assigned rail car manufacturing projects. This role ensures compliance with contract requirements, technical specifications, and industry standards across production, acceptance, warranty, and modification phases. Responsibilities include creating Master Test and Inspection Plans, First Article Inspection schedules, Project Quality Plans, and audit procedures. The Project Quality Engineer coordinates closely with customers, vendors, and internal Kawasaki divisions to align project requirements, resolve quality issues, and support continuous improvement initiatives. This position also monitors documentation, leads corrective action activities, conducts contract reviews, and provides weekly and monthly quality reports. The engineer will serve as a primary Quality liaison between internal teams, subcontractors, and customer Resident Inspectors, ensuring timely communication, follow-up, and delivery of all quality-related commitments. Candidate Fit Summary This candidate is an excellent fit for organizations in the rail, aerospace, transportation, and heavy manufacturing sectors where strict compliance, technical quality standards, and contractual requirements are essential. They bring strong experience supporting complex production programs, managing supplier and customer interfaces, and developing detailed quality documentation. Skilled in FAI, FMEA, audits, and ISO 9001 processes, they excel in environments requiring strict quality controls, cross-functional coordination, and schedule accountability. Their ability to lead inspections, manage customer quality requirements, and drive corrective actions makes them a strong match for production-focused, project-driven engineering organizations. Essential Functions Implement and maintain QA programs for assigned contracts. Develop Master Test and Inspection Plans, Project Quality Plans, FAI schedules, and audit procedures. Attend project meetings and provide detailed quality status updates and reports. Analyze quality issues, identify root causes, and drive corrective actions. Coordinate with customers, suppliers, and internal teams across production and warranty phases. Manage project quality schedules and interface with Resident Inspectors. Ensure compliance with customer specifications, contract terms, and Kawasaki quality standards. Review and approve subcontractor/supplier documentation (PSI, FAI, audits, drawings, field reports). Monitor and report deviations, implement process improvements, and update procedures. Support Configuration Management planning, execution, and product delivery. Assist with subcontractor activity quality review and documentation. Travel domestically/internationally up to 30% to support project quality functions. Job Specifications Bachelor's Degree in Engineering (Master's preferred). Minimum five (5) years' experience in rail, aerospace, transportation, or heavy manufacturing. Knowledge of FAI, FMEA, ISO 9001, and source inspection processes. Strong communication, analytical, reporting, and computer skills. Ability to plan, coordinate, and manage workloads across multiple concurrent projects. Capable of working in both office and field/manufacturing environments. Work Environment Office and manufacturing floor settings. Frequent interaction with engineering, production, and customer teams. PPE required in production areas; must adhere to all safety protocols. Candidate Fit This candidate is a strong fit for Project Quality Engineering roles in complex manufacturing environments like rail, aerospace, automotive, and heavy industrial production. They have demonstrated capability in quality planning, regulatory compliance, supplier oversight, and customer interface management. With experience leading FAIs, audits, and corrective actions while supporting production schedules, they excel in driving continuous improvement, ensuring contract compliance, and maintaining high standards of safety, product quality, and documentation integrity. Their structured approach, technical acumen, and ability to manage project-based workloads make them a key contributor to high-complexity engineering programs. Company Overview Founded in 2010, Top Prospect Group was created with a focus on matching high-quality candidates with top-tier clients while fostering an environment where success is shared by all. In 2023, the company was acquired by HW Staffing Solutions, expanding its service offerings to include technology, engineering, and professional services. Qualified candidates are encouraged to apply immediately! Please include a clean copy of your resume, salary expectations, and availability with your application.

Nationwide Opportunities Do you thrive on optimizing systems, improving yields, and driving operational excellence? Whether your background is in pharma, biotech, medical device, or advanced manufacturing, we'd love to connect. At Scientific Search, we partner with industry leaders and emerging innovators across the U.S. who rely on talented Process Engineers to enhance production efficiency, scale technologies, and ensure consistent product quality. We're continually supporting new searches and always expanding our network of process professionals. We're Interested In Connecting With Engineers Experienced In Process development, scale-up, and optimization Equipment design, installation, and validation Root cause analysis, troubleshooting, and continuous improvement (Six Sigma, Lean) cGMP manufacturing support within regulated environments Cross-functional collaboration with operations, quality, and R&D teams If you'd like to be considered for future Process Engineer roles, please send us your resume. We'll keep you in mind as new positions arise that fit your expertise, interests, and preferred locations. Submit your resume We're always growing our network of skilled Process Engineers - let's stay connected so we can help you discover the right opportunity when the time is right. #19580

Role: QA Engineer App Sr Advanced Tech hybrid 3 days onsite. Duration: Contract Mandatory Skills & Qualifications 10+ years of relevant client-facing experience in QA/testing roles (excluding training periods) Minimum 5 years of on-site client experience in similar technology and domain Educational Requirement: Bachelor's degree in Technology (Master's preferred) Strong hands-on experience with the MERN Stack (MongoDB, Express, React, Node.js) Proficiency in programming/scripting: Java and JavaScript Extensive experience with modern automation tools such as: Selenium WebDriver Cypress or other industry-standard automation frameworks Strong understanding of QA methodologies, SDLC, STLC, Agile/Scrum processes Experience building reusable automation frameworks (UI and/or API) Experience in Performance Testing tools (e.g., JMeter, Locust) - preferred for Group B

Job Description Senior Industrial/Process Engineer New Jersey, Onsite, Full Time 150-200k (Based On Experience) We are a large-scale manufacturing operation in New Jersey, constantly evolving and committed to technical excellence, efficiency, and innovation. Our engineering team includes specialists across multiple disciplines, and we are now seeking a strong, well-rounded leader who can bring these experts together to drive collaboration, growth, and continuous improvement. Position Overview We are seeking a highly experienced and technically strong Senior Engineering Leader who can guide, mentor, and elevate a diverse team of engineers. While each team member specializes in their area-process, industrial, mechanical, automation-the Senior Engineering Leader will unify their efforts, establish standards, and ensure best practices are adopted plant-wide. The right candidate is not just a subject-matter expert but a strategic, big-picture leader who can inspire engineers, lead by example, and drive measurable improvements across all spaces. You'll play a pivotal role in optimizing operations, training your team, and embedding a culture of continuous improvement. The Ideal Candidate A well-rounded senior engineer with deep technical knowledge and leadership presence. Proven ability to unify and guide specialized engineers toward shared goals. Skilled in mentoring, training, and developing technical talent. Naturally curious, always seeking ways to optimize systems, workflows, and operations. Confident communicator who can balance strategic vision with hands-on problem solving. Key Responsibilities Lead, mentor, and develop a multidisciplinary engineering team across process, industrial, and mechanical functions. Establish plant-wide engineering standards and best practices to ensure efficiency, quality, and safety. Partner with specialized engineers to identify challenges, improve workflows, and optimize facility spaces. Drive automation, process upgrades, and system enhancements in alignment with company goals. Promote knowledge sharing and training across engineering disciplines. Support capital expenditure planning, cost models, and ROI analysis. Champion a continuous improvement culture across all engineering functions. Qualifications Bachelor's degree in Mechanical, Industrial, Process, or related Engineering field (Master's preferred). 10-15+ years of engineering experience within manufacturing environments. Strong technical expertise across multiple engineering disciplines (process design, systems optimization, automation, facility layout). Proven leadership track record of managing, training, and growing engineering teams. Experience leading cross-functional initiatives that improved efficiency, cost, or production scalability. Excellent problem-solving, analytical, and project management skills. Strong communication and leadership presence-capable of influencing both technical staff and executive leadership. Must-Haves 10+ years in high-volume manufacturing engineering. Hands-on technical strength plus proven leadership of engineering teams. Experience mentoring engineers and elevating team performance. Demonstrated success leading process optimization and system improvements across multiple disciplines. Benefits Competitive salary and performance-based incentives. Medical, dental, and vision coverage. 401(k) retirement plan with employer contributions. Professional development and training opportunities. A collaborative environment with real impact on large-scale operations. This is an exciting opportunity for a high-level engineer ready to step into a leadership role where you'll unify specialized engineers, mentor rising talent, and drive measurable improvement across a large-scale manufacturing plant. Email Resume: ********************* Apply Online: https://jobs.crelate.com/portal/maiplacement/job/eqr4zdqe388dprs6jnnfkh9tkc?crt=***********73 Refer a friend, get up to $1000!

Job DescriptionDescriptionIn this position, you will be responsible for production data analysis to develop and track the impact of strategic initiatives across our manufacturing facilities in America. You will play a pivotal role in collaborating with resources (including finance and process engineering) at the plants to implement enhanced solutions that improve our manufacturing and financial yields. Key Responsibilities Data Analysis: Analyze and provide detailed summaries and reports for industrial process monitoring, diagnostics and optimization. Utilize data-driven approaches to analyze performance metrics, identify trends, and present actionable insights for improvement. Manufacturing Analysis Systems: Establish, deploy and standardize enhanced data analysis systems across manufacturing facilities in America that will increase factory yields and cost. Cross-Functional Collaboration: Interface with production, quality, engineering, program developers, and finance teams regularly. Facilitate and collaborate with various departments within the factories to develop, track, and summarize initiatives that are driving improvement of critical yield KPIs. Continuous Improvement: Initiate and support continuous process improvement efforts along with the local engineering and finance teams. Structured Problem Solving: Establish, deploy and standardize structured problem solving methodologies and documentation across manufacturing facilities in America, including but not limited to Six Sigma and RCCA, etc. Skills, Knowledge and Expertise Bachelor's degree in Engineering or a related field. Relevant certifications and experience with data analytics is a plus. Proven hands-on experience (5-8 years) in a manufacturing environment, with a focus on process engineering, yield improvements, and data analysis. Excellent communication and leadership abilities to effectively collaborate with cross-functional teams and drive change and participate in root cause analysis. Proficiency in project management and change management principles. Capability for rapid analysis, decision making, and team guidance. Experience with Six Sigma quality and data analysis. Proficiency with Minitab or JMP or equivalent software. Familiarity with creating dashboards and reports for production data- including links between yield, defects, and key attribute data. Critical thinker and sound decision maker with strict attention to detail. Dedication to continuous improvement. Relocate to work in factory at Cazenovia, NY. All applicants must be eligible to work in the US without restriction to ITAR documentation and materials. Must be a US citizen, legal permanent resident, refugee, or asylee BenefitsWhat's in it for you on Day 1: Medical, dental and vision insurance plans Prescription Drug Plans Basic Life Insurance 401k plan with company match Tuition Reimbursement Program Security Clearance Incentive Program Employee Referral Program Overtime opportunities Alternate work schedules available PTO (10 days) and NYS Sick and Safe Leave Paid Holidays Exciting Onsite Perks: Free Starbucks coffee available at our café Free access to our Fitness Center Fresh food is available for purchase in the cafeteria store. Employee Appreciation Events Knowles is committed to providing a competitive and fair total compensation package for all employees. One element in our total compensation package is base pay. The starting salary for this role is targeted to be between $100,000 to $130,000 annually. Individual compensation decisions are based on a number of factors, including but not limited to previous experience and skills acquired prior to joining Knowles, cost of living in the assigned work location, assigned schedule, and salaries of similarly situated peers at the company. It is to be expected that candidates will come to us with different sets of skills and experiences and therefore will be paid at different points in the stated range. We recognize that the person(s) we select for hire may be less experienced or more experienced than the role as posted; if this is the case, any updates to available salary ranges will be communicated with candidates during the recruitment process. Equal Opportunity Statement: Knowles Precision Devices prohibits pay discrimination and discrimination of any kind based on race, color, gender, national origin, age, disability, veteran status, marital status, pregnancy, gender expression or identity, sexual orientation, or other legally protected status. ITAR Statement: Please note that this position may require access to technical data controlled under the International Traffic in Arms Regulations (ITAR) or Export Administration Regulations (EAR). Applicants must be U.S. persons (citizens, lawful permanent residents, or individuals granted refugee or asylee status) or have the necessary authorization to access controlled technical data. Compliance with ITAR and EAR regulations is a condition of employment. Notice to Staffing Agencies, Search Firms and Recruitment Agencies: The recruitment process at Knowles is managed through the Human Resources department. Knowles does not accept resumes submitted from 3rd party agencies outside of our system. To submit resumes, 3rd party agencies will need to be a pre-approved vendor with a valid contract in place, be actively engaged by Knowles to recruit for a specific position and have agency log in credentials to submit candidates to our careers portal. Please do not submit resumes via e-mail, through our external website or directly to our employees. Any resumes submitted in this way become the property of Knowles and will not be eligible for any placement fee.

We are seeking a detail-oriented and collaborative Manufacturing Engineer to support both New Product Introduction (NPI) and existing product lines. This role serves as a critical link between engineering, operations, and customers, ensuring 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. The position requires a strong focus on Design for Manufacturability (DFM), acting as a key liaison between customers and internal teams to ensure 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 senior 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 * SolidWorks * Design for manufacturing * Mechanical design * GD&T * Manufacturing and machining * Mechanical design (tooling and fixture design) * CAD - SolidWorks * GD&T, Manufacturing engineering * Continuous improvement * Lean manufacturing * Six sigma * Tooling * Engineering * Machining * Sheet metal 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. * Strong understanding of 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. * Proficiency in CAD software and Microsoft Office Suite. * Demonstrated ability to lead cross-functional teams and drive process improvements. * Familiarity with CNC machining and quality assurance processes is a plus. Work Environment The work environment consists of 130 total employees in Elmwood Park, including 3 manufacturing engineers and 5 CNC Applications Engineers. Employees work cross-functionally with engineering and production, and are involved with customer interactions and seeing projects from quote through execution to shipment. 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. getting benefits from client Workplace Type This is a fully onsite position in Elmwood Park,NJ. Application Deadline This position is anticipated to close on Dec 8, 2025. 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.

Primary Duties & Responsibilities Process Development: Apply engineering principles to sustain and improve current manufacturing processes Optimization: Monitor, optimize and streamline manufacturing processes including production flow, manpower requirements, assembly methods and production equipment. Continuously analyze and improve processes to improve yield, enhance productivity, reduce waste, and lower costs. New Production Introduction: Lead the introduction of new products into the process, ensuring smooth transitions from prototype to full-scale production. Tooling and Equipment: Select and implement appropriate tooling and equipment for operations, ensuring compatibility and efficiency. Quality Assurance: Establish and maintain quality control standards and procedures to ensure products meet or exceed specifications. Monitor manufacturing areas to proactively assess product quality and ensure compliance with ISO guidelines and procedures Troubleshooting: Identify and resolve issues related to processes, equipment, and tooling. Documentation: Create and maintain detailed documentation of processes, including work instructions, process flows, and control plans. Collaboration: Using Lean/Kaizen methods, monitor and improve the efficiency, output and safety of manufacturing processes through observations and measurements as well as by collecting and interpreting data from databases, hard copies and other technical and manufacturing personnel Training: Provide training and support to production staff on best practices. Continuous Improvement: Lead and participate in continuous improvement initiatives to enhance overall manufacturing performance. Using Lean/Kaizen methods, monitor and improve the efficiency, output and safety of manufacturing processes through observations and measurements as well as by collecting and interpreting data from databases, hard copies and other technical and manufacturing personnel Education & Experience Bachelor's degree in Engineering required. Chemical, Mechanical, Manufacturing, or Material Science Engineering preferred Minimum 3 years of process engineering experience in a similar industry. Excellent problem-solving and analytical skills. Skills Experience using materials processing equipment such as furnaces, ovens, programmable controllers, powder mixing, foundry tools, etc. Experience with materials characterization tools and methods for microscopy, chemistry, structural properties, thermal properties, etc. Experience with inspection equipment, including CMM, hand tools, visual tools, etc. Working knowledge of design, inspection and process control software (CAD, CMM, PLC) Working knowledge of data analysis tools (SPC, MiniTab and DoE) Experience with problem solving and resolution (8D, fishbone, etc.) Demonstrated ability to achieve results independently or working with others Hands-on and very direct approach to problem solving Excellent interpersonal and communication skills Experience with networked PC based computer systems (MS Office, spreadsheets, data bases, graphics, Email, MRP systems, etc.) Experience in ceramic fabrication preferred Excellent communication and interpersonal skills Commitment to continuous improvement Proactively takes actions to address customer needs and issues. Regularly works independently with minimal supervision to achieve goals and objectives. Knowledge of Lean Manufacturing principles and Six Sigma methodologies is a plus. Working Conditions Shopfloor, laboratory, and office environments. Occasional travel may be required. Physical Requirements Ability to lift and carry up to 25 pounds. Able to sit, stand, bend, squat and walk about the facility. Walk of uneven and slippery surfaces Ability to work at a computer for extended periods. Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities This position may be responsible for the execution and maintenance of the ISO 9001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. To conform to U.S. Government export regulations (ITAR), applicant must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8. U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State."

Job DescriptionBenefits: 401(k) 401(k) matching Bonus based on performance Company parties Competitive salary Employee discounts Free uniforms Paid time off Mid-Level Manufacturing Engineer (Windows & Doors) Location: Queens, NY (on-site) Department: Engineering / Operations Reports To: VP Operations Type: Full-time Role Summary Were looking for a hands-on Manufacturing Engineer (3+ years) to drive throughput, quality, and cost reduction across our window manufacturing lines (vinyl/aluminum). Youll own process improvement, tooling/fixtures, new equipment integration, and production supportpartnering closely with Production, Quality, Maintenance, and Sales to keep jobs moving and customers happy. Key Responsibilities Process Optimization: Map current state, remove bottlenecks, and improve takt/OEE, scrap, and first-pass yield using lean/5S/Kaizen. Equipment & Tooling: Specify and commission machinery (e.g., double-miter saws, 4-head welders, corner cleaners, hardware stations, IGU line); design jigs/fixtures; create preventive maintenance plans with Maintenance. Assist the mechanic with troubleshooting equipment and minimizing downtime. Standard Work & Documentation: Build/maintain SOPs, WIs, control plans, PFMEA; train operators and line leads. Quality Engineering: Analyze defects/returns; implement corrective actions aligned to AAMA/NFRC and relevant ASTM performance standards (air/water/structural/thermal). New Product Introduction: Industrialize new profiles/assemblies BOM/routing setup, pilot runs, capability studies, and ramp-to-rate. Data & Cost: Track line metrics (OEE, downtime, changeover, scrap); partner with Supply Chain on yield, alternative materials, and vendor qualifications. Safety & Compliance: Engineer guards/ergonomics; support OSHA and electrical/mechanical safety on the floor. Qualifications 35+ years in manufacturing/industrial engineering (windows/fenestration, building products, or discrete fabrication strongly preferred). BS in Mechanical, Industrial, or Manufacturing Engineering (or equivalent experience). Ability to read and write in Chinese Proficiency with CAD (SolidWorks/AutoCAD) and MS Office. Demonstrated lean toolkit (5S, SMED, value-stream mapping, root cause/8D). Comfortable on the floordiagnosing issues at machines, with operators, and vendors. Nice to Have Experience with IGU processes (spacer/butyl/hot-melt, gas fill), vinyl welding parameters, aluminum fabrication, and hardware installation cells. Basic statistics/DOE; gauge R familiarity with AAMA/NFRC audits. Exposure to PLC/HMI basics and machine safety. What Success Looks Like (First 90180 Days) Launch 5S + Standard Work in one of the three production lines (vinyl production); OEE +10% and scrap 15%. Improve QC satisfactory results by 30%. Implement PM checklists on priority machines; unplanned downtime 20%. Compensation & Benefits Salary: $70,000$85,000 base + performance bonus; PTO, holidays, 401(k) match, and continuing education/self-improvement course expense reimbursement. Schedule & Work Environment MondayFriday, primarily day shift; occasional off-shift support for trials/startups. Office adjacent to production; frequent time on the floor with PPE. Equal Opportunity Employer. We value diversity and provide equal employment opportunities to all employees and applicants.

Job description: Company Description: Our long term client is a growing manufacturing company specializing in precision machining and fabrication. They are currently seeking an experienced Manufacturing Engineer to join their team. If you are a skilled professional with a strong background in CNC machining, CNC programming, blueprint reading, and setup operations, Budgeting, Capital Equipment Instillation, Fixture Design, Designing in Solidworks, we want to hear from you! Position Overview: As a CNC Manufacturing Engineer, you will play a crucial role in producing high-quality machined components for a variety of industries such as the aerospace, automotive and medical device industries that require tight tolerance machining. You will be responsible for setting up, operating, and programming CNC machines (Lathes), interpreting blueprints, adjusting tooling, making offsets, and using precision measurement tools to ensure the accuracy of the final products. Your expertise will contribute to the success of their operations. Key Responsibilities: Design, draw up, produce on CNC machinery, inspect, and validate manufacturing process, assembly or parts, and test fixtures made for production. Manage projects with buyers, other design engineers, test engineers on scheduling, and prioritizing of job orders. Set up, operate, and program Fanuc controlled - CNC Lathes, Mills, using Solidworks, MasterCam or other CAM software in accordance with production specifications. Create new and revise existing assembly procedures, work instructions, part protection procedures, standards, etc. Read and interpret blueprints and engineering drawings to ensure the accurate machining of components. Upload programs and make necessary adjustments to machine parameters. Select and install appropriate tooling and make tooling offsets as needed. Monitor and maintain quality control throughout the machining process. Qualifications: BS in Mechanical or Industrial Engineering or the technical equivalent Minimum of 3 years of CNC manufacturing experience. Minimum 3yrs of CNC Programming experience. Proficiency in setting up and operating CNC machines. Solid Works Preferred. Strong blueprint reading skills. Ability to read and understand CNC programs (G & M codes - Fanuc control). Knowledge of tool selection, tooling setup, and making tool offsets. Proficiency in using metrology tools (CMM experience is a plus) Understanding of Six Sigma and Lean manufacturing tools Strong attention to detail and commitment to producing high-quality work. Strong problem-solving skills and the ability to troubleshoot machine issues. Good communication skills and the ability to work effectively in a team. Willingness to work with a safety-first mindset. Hours/Shifts: 1st Shift Mon-Fri. 7:00am to 3:30pm Overtime available Benefits: Health Insurance - Single or Family 401k with Company Match Holiday Bonuses Performance bonuses Possible tuition reimbursement Salary Range: $95-150K DOE

Roquette is a family-owned global leader in plant-based ingredients and a leading provider of pharmaceutical excipients. Want to help us make a difference? Using plant-based resources, we collaborate with our customers and partners to imagine and offer ingredients to better feed people and treat patients. Each of our ingredients responds to unique and essential needs, and they enable healthier lifestyles. The Role: We are looking for our next Process Engineer II within our Operations Team. The Process Engineer II will be responsible for supporting day-to-day support of production processes and developing and implementing improvements to existing processes and products in order to meet Corporate and customer standards. This position is located in Newark, Delaware. Compensation: The current salary range for this role is estimated to be $99,000 - $134,000. In addition, this position may also be eligible to earn performance-based incentive compensation. The specific compensation offered to a candidate will be influenced by a variety of factors including but not limited to skills, qualifications, experience, and location. What You'll Do: Troubleshoot process problems in operations. Identify and develop process changes and modifications to enhance operating reliability and product quality and to improve efficiencies of key resources. Monitor environmental regulations and performance against such as it pertains to project areas. Identify and develop control mechanisms to improve reliability and efficiency of plant operations. Commission installations in a timely and effective manner. Operating Services Agreement Activities (Services provided 3rd party owner of one production line) Coordinate operations activities between Roquette and third-party owner Maintain communications for operations issues, changes, etc. between Roquette and third-party owner Facilitate process improvements for third-party process and assets Provide technical support for third-party process Provide daily technical oversight and guidance for colloidal manufacturing process Write operating procedures and train operators on start-ups and integration of new systems. Lead or participate in Root Cause Failure Analysis (RCFA) pertaining to deviations, incident investigations, complaints, etc. Understand and track key performance indicators for the manufacturing process, including process yields, rates, etc. Participate in safety and health policies and procedures by ensuring that all processes and modifications to existing processes have been critically reviewed for safety and health and environmental considerations. Participate in hazardous operations reviews and project safety reviews. Ensure all changes, new processes and equipment has been reviewed and complies with current Good Manufacturing Procedures (cGMP), ISO and other quality and regulatory standards. Support the plant's safety, health & wellness environmental and industrial hygiene programs. Evaluate process changes, new processes and equipment, etc., to determine requirements for measurement accuracy for plant instruments and equipment. Proactively network with other Engineering technical disciplines (e.g., Consultants for Materials, Engineering Mechanics, Instruments & Process Controls, Electrical and Energy), plant and business personnel, and suppliers and contractors to improve process reliability, quality, and safety. Develop engineering solutions for chronic and sporadic process problems and collaborate with technical, operations, and maintenance to implement solutions. What You'll Need: Education: B.S. degree in chemical engineering or related engineering field. Experience: >2-3 years of experience in manufacturing operations or equivalent experience preferred. Experience in food/pharma manufacturing operations preferred. Ability to read, spell, comprehend, and perform and apply basic math skills. Excellent computer aptitude, communication and interpersonal skills. Strong Computer skills Self-directed and self-motivated Solid written and oral communication skills. Ability to work as a team member in a respectful manner in a diverse work environment. Strong analytical skills with demonstrated ability to consistently solve problems in a decisive and efficient manner. Demonstrates expertise of statistical analysis to be used for process improvement. Demonstrates expertise of root cause analysis methodologies. Demonstrates expertise of quality control procedures, processing equipment and plant utilities, or equivalent experience at a manufacturing plant. Interpersonal skills for working in teams across functions. Experience using and understanding of Enterprise Resource Planning (ERP) and software systems such as SAP , FMEA+, database/SQL infrastructures, and document control a plus. Six Sigma Greenbelt certified, experience with 5S, and understanding of lean principles a plus. Work Environment This role spends approximately 50% of the time in an office environment and 50% of the time in the plant environment. Physical Demands While performing the duties of this job, the employee is required to speak or hear. The employee is frequently required to stand; walk, climb stairs, use hands and fingers to handle or feel; and reach with hands and arms; work in hot, cold and loud environments. Position Type/Expected Hours of Work This is a full-time position. Days and flexible hours of work are required to meet facility demands. Business Travel: Travel, some internationally, may be required when collaborating with other manufacturing facilities, for training, etc. AAP/EEO Statement Roquette is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national origin, gender, sexual orientation, gender identity, age, physical or mental disability, genetic factors, military/veteran status or other characteristics protected by law. “AAP, EEO, Drug-Free Workplace” Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. If you identify yourself in this position, please apply by uploading your resume and let's start the journey together! Roquette is proud to be a global company where you can find personal and professional growth through multiple diverse experiences. Roquette strives to create a dynamic workforce while remaining firmly committed to equal opportunity by complying with EEO laws. As we continue to grow, Roquette understands that to be successful we must always be inclusive in our approach. To find out more about our products, values and sustainable development ambitions visit us at **************** and at *******************************

Associate Process Engineer/Scientist- Drug Product, Biologics Manufacturing Science and Technology Key responsibilities include • Execution of post-market process change activities/experiments through partnership with R&D development assets • Responsible for characterizing, optimizing and troubleshooting product and manufacturing processes of parenteral dosage forms. • Work with R&D and manufacturing sites to design and execute experiments to support product robustness, new technology implementation, and/or manufacturing investigations • Serve as technical resource to other functions, providing expertise on the product and its process. • Effectively represent biologics drug product manufacturing science and technology in various internal and external teams and committees on development, technology transfer, manufacturing, specifications, process validations and launch. • Provide assistance to sites globally to resolve significant quality events and manage complex change controls. Qualifications • Bachelor's degree in relevant science or engineering discipline (chemistry, pharmaceutical sciences, pharmacy, biology, chemical engineering). • Master or advanced degree preferred. • Minimum of 3-5 years of experience in the Pharmaceutical or Biotechnology industry in product and process development and commercialization in a global environment. Key Skills and Experience • Hands-on experience in the laboratory and in-depth understanding in sterile and liquid products, particularly biologics, formulation development, analytical methods, commercial manufacturing, and their unit operations. • In-depth understanding of Quality by Design (QbD), Design of Experiments (DOE), multivariate analysis, PAT, critical process and material attributes and CQA's. • Working competency of Statistical Process Control and related tools (JMP/MiniTab/SAS). • Able to design and execute scientifically sound, hypothesis driven experiments • Skilled in writing and reviewing complex study plans and scientific reports. • Possess high level of familiarity with sterile product processing equipment and manufacturing facilities. • Overall knowledge of parenteral technology: aseptic processing, sterilization, isolator processing, lyophilization, pre-filled syringe operations, etc. • Strong understanding of project management systems and tools • Six Sigma Green/Black Belt certification desirable Additional Information Interested candidates may contact at "Praveen.arora(@)artechinfo.com or ************

Job Description iRocket (Innovative Rocket Technologies Inc.) is pioneering fully autonomous, fully reusable small launch vehicles for responsive access to space. We leverage cutting-edge propulsion, reuse, and sustainable propellant technologies to make launch more frequent, lower cost, and eco-friendly. We are headquartered in New Hyde Park, NY. The Role As a Machining & Manufacturing Engineer at iRocket, you will own the development, optimization, and scaling of high-precision manufacturing processes for rocket hardware. You will work cross-functionally with design, test, supply chain, and quality teams to mature processes from prototype through production. You will report to the Senior Manager of Manufacturing Engineering. Develop, validate, and refine machining processes (CNC turning, milling, EDM, grinding, etc.) for rocket components Collaborate with design engineers to ensure manufacturability, offer design for manufacturing (DFM) feedback, and propose design changes where beneficial Create and maintain manufacturing BOMs, process flows, work instructions, and SOPs Support installation, calibration, qualification, and commissioning of new machines and tooling Lead root cause analysis (RCA) for production issues and drive corrective and preventive actions Implement process controls, error-proofing, statistical monitoring, and quality gates Participate in manufacturability reviews and design reviews to provide input from a manufacturing perspective Document and drive continuous improvement in process maturity, standardization, and scaling Support aerospace / defense compliance efforts (e.g. AS9100, aerospace quality standards) Occasionally support mission-critical deadlines which may require non-standard hours Requirements Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, or a related discipline 3+ years of experience in machining / manufacturing engineering in aerospace, defense, or precision industries Strong knowledge of GD&T, tolerancing, fixtures, tooling, materials, machining best practices Hands-on experience developing machining processes, tooling, fixturing Proficiency in reading engineering drawings, specifications, and technical documentation Ability to work cross-functionally, strong problem solving, and data analysis skills Excellent communication skills (verbal and written) Master's degree in Mechanical or Manufacturing Engineering Experience with aerospace quality systems (AS9100, NADCAP, etc.) Familiarity with additive manufacturing, welding, exotic materials, or hybrid manufacturing methods Experience with lean manufacturing, continuous improvement methodologies (Six Sigma, Kaizen) Proficiency in CAD/CAM or manufacturing software (e.g. NX, SolidWorks, Mastercam, etc.) Experience in propulsion, space, or high-reliability systems Benefits Health Care Plan (Medical, Dental & Vision) Retirement Plan (401k, IRA) Life Insurance (Basic, Voluntary & AD&D) Paid Time Off (Vacation, Sick & Public Holidays) Family Leave (Maternity, Paternity) Short Term & Long Term Disability Wellness Resources

Details: L.J. Gonzer Associates is looking for individuals to join our pool of qualified candidates for potential assignment as a Manufacturing Engineer. Responsibilities will include: Conduct all work in a safe manner For NPI programs, with input from design and test engineers, determine all needed assembly and test fixtures (create fixture list). Design, draw, have manufactured, inspect, and validate manufacturing, assembly, and test fixtures. For NPI programs, coordinate with planner/buyer, design & test engineers on fixture jobs/PO's, priority, and schedule. Develop new and improve existing manufacturing, assembly, and test processes and cells. Create new and revise existing routers, driven by ECO's, process improvements, etc. Update jobs based on NCMR's, ECO's/EO's, redlines, etc. Create jobs to make fixtures or development parts. Review and approve ECO's for new and changes to existing drawings, documents, etc. Review, provide feedback, and offer alternatives regarding NPI drawings for correctness, manufacturability, standardization, best practices, and lessons learned. Build development and LRIP assemblies. Create new and revise existing assembly procedures, work instructions, part protection procedures, standards, etc. Determine and implement part protection and handling processes to reduce damage and rework. Provide all needed support for final packaging, E.G., process, materials, documentation, etc. Prepare ECO's for new and changes to fixture drawings, weld simulation drawings, standards, etc. Lead or support the identification and removal of waste from manufacturing, assembly, and test processes. Lead or support cross functional teams. Lead or support structured problem solving / root cause corrective actions to address systemic quality problems. Lead or support capital expense efforts. Details: BS in Mechanical or Industrial Engineering or the technical equivalent. 2+ years of manufacturing engineering or relevant experience. Experience with fixture design. Understanding of Six Sigma and Lean manufacturing tools. Proficient in the use of SolidWorks. Solid project management, communication, and cross functional team leadership skills. Ability to perform in a fast paced, medium sized company. Results oriented and ability to motivate team members.

Join Weiss-Aug - A Leader in Precision Manufacturing and Innovation Be part of a company that's shaping the future of manufacturing where your ideas, skills, and passion matter. Weiss-Aug, is a leading provider of advanced manufacturing and engineering solutions with advanced facilities across the U.S. and Mexico for over 50 years. Why Join Us? At Weiss-Aug we are driven by a commitment to excellence, innovation, and continuous improvement. As a recognized leader in the industrial and commercial sectors, specializing in high-volume metal stamping, thermoplastic molding, and value-added assembly solutions for the medical, aerospace & defense, automotive, interconnect, telecommunications and consumer goods industries, we take pride in cultivating a collaborative and forward-thinking work environment. We're currently seeking a passionate and skilled Manufacturing Engineer to join our team and contribute to our mission of delivering high-quality, engineered solutions to our customers worldwide. In this role you will be responsible for supporting our manufacturing operations. As a Manufacturing Operations Engineer, you will be tasked with driving impactful, technical projects which improve product quality, lower production costs, and improve productivity while ensuring strict adherence to safety, quality, and industry standards. Responsibilities Conduct projects to simplify work processes, improve tooling, improve throughput, reduce scrap, and ensure equipment reliability. Collaborate with other departments to investigate and address quality-related issues using methodologies like 8D, Kaizen, DMAIC, and root cause analysis. Develop and maintain production-related documentation and Standard Operating Procedures (SOPs). Work alongside production supervisors, operators, toolmakers and maintenance staff to identify and address production needs. Provide guidance for designing and troubleshooting automation systems. Troubleshoot technical challenges in production, identify root causes, implement solutions, and monitor their effectiveness using empirical data. Work with cost accountants to understand opportunities for improvement to the process which will lead to improved financial performance. Design and deploy essential tools, fixtures, or equipment to boost production efficiency, reduce errors, improve inspections, and improve ergonomics. Develop lean cell layouts and workflows to minimize waste and enhance productivity / ergonomics. Maintain professional and technical expertise by attending tradeshows and continuing education workshops. Participate in PPAP process, including drawing feasibility reviews, manufacturing reviews, Failure Modes and Effects Analyses (FMEAs) reviews, etc. Requirements BS degree in Mechanical Engineering, Manufacturing/Industrial Engineering, or equivalent. Must possess good analytical and problem-solving skills and mechanical aptitude. 5-10 years minimum experience in a medium/high volume manufacturing environment. Strong understanding of Continuous Improvement, Six Sigma, 5S, and Lean manufacturing tools. Comfortable with hands-on interaction with mechanical and electrical components. 3D CAD experience in SolidWorks strongly preferred. GD&T experience preferred. Experience with automation design and/or programming a plus. Experience with vision system technology a plus. ERP experience a plus. Must be driven self-starter that works with little supervision. Must have good written and verbal communication skills. Must possess the ability to multi-task and set priorities. Must be a Team player and have the ability to interact effectively with all departments within the Company. Must have good windows-based PC skills (Microsoft Office, Outlook, Excel, etc). Must be familiar with time studies. ISO/QS knowledge a plus. Plastic Injection/Insert Molding and/or Progressive Stamping Experience a plus. Additional Notes This role will require you to be 100% on site our East Hanover, NJ location. Relocation assistance is not available for this position Pay Range: $100k-$125k Other Benefits Include Medical, Dental and Vision 401 (k) with company match Holiday, Vacation and Sick Time Tuition Reimbursement Health Savings Accounts (HAS) Flexible Spending Accounts (FSA) Cigna Wellness Incentive Program Employee Assistance Program (EAP) Short Term Disability Group Life and Accidental Insurance Sun Life - Accident, Critical Illness, and Hospital Indemnity Insurance Smoking Cessation Program Pet Insurance US Pay Transparency The base salary for this role will be determined on a case-by-case basis and may vary based on the following considerations: job-related knowledge and skills, experience, and internal consistency. If your salary requirements exceed the advertised range and you remain interested in Weiss-Aug, we encourage you to apply. Weiss-Aug is an Equal Opportunity/Affirmative Action Employer. Applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, protected veteran status, disability, or any other characteristics protected by applicable federal, state, or local law. Notice to Agency and Search Firm Representatives: the Weiss-Aug Group is not accepting unsolicited emails from agencies and/or search firms for this job posting.

Shift: Weekend night shift: Sat. - Mon..: 5:45PM - 5:55 AM What You Will Do: Job Title: MFG Processor Mix raw materials according to formula sheet instructions efficiently and safely within the established quality and production standards to manufacture bulk used to produce finished product. Responsible for autonomous maintenance and change overs to ensure good working order of equipment. What We Are Looking For: * High school diploma or equivalent * Minimum 1 year manufacturing, processing and mixing experience * Able to read and understand scales calibrated in metric format and be able to use the metric system in all aspects of this position. * Color matching skills preferred * Able to complete forklift and respirators certification What's In It For YOU: * Safety-centric Environment with Inclusive Mindset & Culture * Competitive Pay + Profit Sharing * Pension Plan + 401K w/ Company Match * Flexible Time Off: 30 Paid Days Off a Year * Full Benefit Package (Medical, Dental, Vision, HSA) * Free & Discounted Products @ L'Oréal Company Store * Paid Parental Leave Additional Benefits: Shift Differential & Opportunity for Overtime, Growing business with opportunity for advancement, Vacation purchase plan, Learning & Development Opportunities, Employee Resource Groups, Access to Mental Health & Wellness Programs, Tuition Reimbursement, Clean & Climate-controlled environment Full below: Job Title Processor, Weekend night shift: Sat. - Mon..: 5:45PM - 5:55 AM Division: L'Oréal Dermatological Beauty Location: Somerset, NJ Reports To: Senior Manager, Processing Who We Are: For more than a century, L'Oréal has devoted its energy, innovation, and scientific excellence solely to one business: Beauty. Our goal is to offer each and every person around the world the best of beauty in terms of quality, efficacy, safety, sincerity and responsibility to satisfy all beauty needs and desires in their infinite diversity. At L'Oréal Dermatological Beauty, our mission is to help everyone in their quest for healthy and beautiful skin. Our division is the world leader in dermo-cosmetics by adding health to beauty. Our brands portfolio includes CeraVe, La Roche-Possay, Vichy, SkinCeuticals offering a range of skincare and haircare products to respond to all expectations linked to beauty and health of the skin. What You Will Learn: Mix raw materials according to formula sheet instructions efficiently and safely within the established quality and production standards to manufacture bulk used to produce finished product. Responsible for autonomous maintenance and change overs to ensure good working order of equipment. * Operates automatic and manual chemical process equipment in accordance with operating procedures and in a safe manner. Equipment includes mixers, grinders, filter presses, dryers, filtering equipment, pumps and filling machines. Responsible for PUR, change over time, waste and other losses. * Performs quality control analysis as required to complete in-process batches and identifies variations. Processes generate high pressure and critical reactions and processor must execute correct response based on hazardous material and emergency training. * Adhere to GMP's/SOP's housekeeping standards and all site safety policies * Identify potential risks, resolve issues, audits standards/processes to exceed quality and safety standards and conducts root cause analysis. * Provides continuous improvement efforts and validates with Quality team prior to implementation. * Comply 100% with all documentation requirements (OTC, Cleaning, safety checklist, etc.) * Utilize systems (ISIS, Flexnet) to report on KPIs, equipment performance, etc * Perform daily functions of processing, pre-weigh or sanitization. Pre-weigh raw materials, labels, transact and store for production. Clean and sanitize equipment as required. * Retrieve supplies from warehouse/storage area * Process bulk in accordance with IQ procedures What We Are Looking For: Required Qualifications: * Education: High school diploma or equivalent * Experience: 1-2 years manufacturing, processing and mixing experience needed. * Demonstrate basic essential mathematical skills of addition and subtraction. * Must be able to read and understand scales calibrated in metric format and be able to use the metric system in all aspects of this position. * Strong interpersonal skills and good communication skills. * Self-starter; enthusiastic to work in a fast paced, team-oriented environment. * Color matching skills preferred * Certify to wear respirators. * Complete forklift certification. What's In It For You: * Competitive Benefit Package (Medical, Dental, Vision, 401K, Pension Plan) * Base Hourly Pay Range: $22.36 - $30.77 (The actual compensation will depend on a variety of job-related factors which may include shift differential, geographic location, work experience, education, and skill level) * Flexible Time Off (Paid Company Holidays, Paid Vacation, Vacation Buy Program, Volunteer Time, Summer Fridays & More!) * Access to Company Perks (VIP Access to L'Oréal's Internal Shop for Discounted Products, Monthly Mobile Allowance) * Learning & Development Opportunities for Career Progression (Unlimited Access to E-learnings, Lunch & Learn Sessions, Mentorship Programs, & More!) * Employee Resource Groups (Think Tanks and Innovation Squads) * Access to Mental Health & Wellness Programs Don't meet every single requirement? At L'Oréal, we are dedicated to building a diverse, inclusive, and innovative workplace. If you're excited about this role but your past experience doesn't align perfectly with the qualifications listed in the job description, we encourage you to apply anyways! You may just be the right candidate for this or other roles! We are an Equal Opportunity Employer and take pride in a diverse environment. We would love to find out more about you as a candidate and do not discriminate in recruitment, hiring, training, promotion, or other employment practices for reasons of race, color, religion, gender, sexual orientation, national origin, age, marital or veteran status, medical condition or disability, or any other legally protected status. If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to access job openings or apply for a job on this site as a result of your disability. You can request reasonable accommodations by contacting [email protected]. If you need assistance to accommodate a disability, you may request an accommodation at any time. Our Safe Together Plan: Your safety is our highest priority. We will proceed with caution and adhere to enhanced protection standards to ensure our sites are safe for all employees. We must all operate with the shared responsibility for each other's health & safety in mind.

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 Fasted 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.

Job DescriptionDescriptionThe Process Engineering group at Knowles Precision Devices is responsible for supporting and maintaining the flow of production material for the Thin Film Product Line. The Knowles Thin Film Product Line includes RF and Microwave components for applications in telecom, aerospace and defense markets. This position is a hands-on engineering role, providing daily support to operations to maintain the flow of parts, implementing new equipment and supporting a range of improvement projects. This is a fast paced position, that expects time management to support short term and long term needs of the company. Salary and title dependent on experience. Key Responsibilities Maintain and develop Job Instructions and Work Instructions for existing and new processes Collect and analyze data on yields and process capability Provide technical skill training to operators Provide process support to minimize production down-time in assigned areas Participate in project based teams Support equipment troubleshooting and maintenance Participate in Material Review Board (MRB) for Root Cause investigations May support contract review and process rulebook maintenance, in support of new product designs Comply with and support company policies and programs regarding safety, security, ISO, EEO, OSHA Skills, Knowledge and Expertise 3+ years of experience supporting laser drilling/cutting equipment in a manufacturing environment Bachelors of Science in engineering/science, or equivalent experience Experience reading and understanding CAD engineering drawings using GD&T Experience measuring and validating workmanship to drawing specification, with optical measurement devices Ability to generate machine motion control programs (i.e. G-Code) Experience authoring job instructions and work instructions Proficiency in statistical methods (DOE, SPC, FMEA) and data analysis tools (e.g., JMP, Minitab, MATLAB, Python, SQL) Strong written and verbal communication skills, communicating to both operators and management Willingness to train others and work as a member of inter-disciplinary teams Must be able to perform lab duties in an ISO certified clean room, meeting gowning, ESD, and EHS requirements. Due to US Export Regulations all candidates must be a U.S. person (i.e. U.S. Citizen, lawful permanent resident, or protected individual) BenefitsWhat's in it for you on Day 1: Medical, dental and vision insurance plans Prescription Drug Plans Basic Life Insurance 401k plan with company match Tuition Reimbursement Program Security Clearance Incentive Program Employee Referral Program Overtime opportunities Alternate work schedules available PTO (10 days) and NYS Sick and Safe Leave Paid Holidays Exciting Onsite Perks: Free Starbucks coffee available at our café Free access to our Fitness Center Fresh food is available for purchase in the cafeteria store. Employee Appreciation Events Knowles is committed to providing a competitive and fair total compensation package for all employees. One element in our total compensation package is base pay. The starting salary for this role is targeted to be between $80,000 to $130,000 annually. Individual compensation decisions are based on a number of factors, including but not limited to previous experience and skills acquired prior to joining Knowles, cost of living in the assigned work location, assigned schedule, and salaries of similarly situated peers at the company. It is to be expected that candidates will come to us with different sets of skills and experiences and therefore will be paid at different points in the stated range. We recognize that the person(s) we select for hire may be less experienced or more experienced than the role as posted; if this is the case, any updates to available salary ranges will be communicated with candidates during the recruitment process. Equal Opportunity Statement: Knowles Precision Devices prohibits pay discrimination and discrimination of any kind based on race, color, gender, national origin, age, disability, veteran status, marital status, pregnancy, gender expression or identity, sexual orientation, or other legally protected status. ITAR Statement: Please note that this position may require access to technical data controlled under the International Traffic in Arms Regulations (ITAR) or Export Administration Regulations (EAR). Applicants must be U.S. persons (citizens, lawful permanent residents, or individuals granted refugee or asylee status) or have the necessary authorization to access controlled technical data. Compliance with ITAR and EAR regulations is a condition of employment. Notice to Staffing Agencies, Search Firms and Recruitment Agencies: The recruitment process at Knowles is managed through the Human Resources department. Knowles does not accept resumes submitted from 3rd party agencies outside of our system. To submit resumes, 3rd party agencies will need to be a pre-approved vendor with a valid contract in place, be actively engaged by Knowles to recruit for a specific position and have agency log in credentials to submit candidates to our careers portal. Please do not submit resumes via e-mail, through our external website or directly to our employees. Any resumes submitted in this way become the property of Knowles and will not be eligible for any placement fee.

Associate Process Engineer/Scientist- Drug Product, Biologics Manufacturing Science and Technology Key responsibilities include • Execution of post-market process change activities/experiments through partnership with R&D development assets • Responsible for characterizing, optimizing and troubleshooting product and manufacturing processes of parenteral dosage forms. • Work with R&D and manufacturing sites to design and execute experiments to support product robustness, new technology implementation, and/or manufacturing investigations • Serve as technical resource to other functions, providing expertise on the product and its process. • Effectively represent biologics drug product manufacturing science and technology in various internal and external teams and committees on development, technology transfer, manufacturing, specifications, process validations and launch. • Provide assistance to sites globally to resolve significant quality events and manage complex change controls. Qualifications • Bachelor's degree in relevant science or engineering discipline (chemistry, pharmaceutical sciences, pharmacy, biology, chemical engineering). • Master or advanced degree preferred. • Minimum of 3-5 years of experience in the Pharmaceutical or Biotechnology industry in product and process development and commercialization in a global environment. Key Skills and Experience • Hands-on experience in the laboratory and in-depth understanding in sterile and liquid products, particularly biologics, formulation development, analytical methods, commercial manufacturing, and their unit operations. • In-depth understanding of Quality by Design (QbD), Design of Experiments (DOE), multivariate analysis, PAT, critical process and material attributes and CQA's. • Working competency of Statistical Process Control and related tools (JMP/MiniTab/SAS). • Able to design and execute scientifically sound, hypothesis driven experiments • Skilled in writing and reviewing complex study plans and scientific reports. • Possess high level of familiarity with sterile product processing equipment and manufacturing facilities. • Overall knowledge of parenteral technology: aseptic processing, sterilization, isolator processing, lyophilization, pre-filled syringe operations, etc. • Strong understanding of project management systems and tools • Six Sigma Green/Black Belt certification desirable Additional Information Interested candidates may contact at "Praveen.arora(@)artechinfo.com or ************