Quality engineer jobs in New Hampshire

Global Quality Manager (CBS) Green, Nashua, Mexicali, Nantong, Hanoi) Amphenol Cable Backplane Systems (CBS) operates at an extreme pace with rapid growth, driven by the global AI hardware infrastructure expansion. As the leading supplier of complex cabled backplane systems, CBS enables next-generation data center performance for technology titans. Our solutions involve thousands of twin-ax subassemblies packaged into custom mechanical assemblies with tightly controlled electrical and mechanical specifications. CBS supports customers from early concept development through full-scale datacenter deployment, ensuring reliability and precision at every stage. The CBS team is looking for a Global Quality Manager. The Global Quality Manager will lead the end-to-end global Quality strategy for Cable Backplane Systems (CBS), ensuring product and process quality across NPI and volume manufacturing, driving customer satisfaction, and reducing field returns through robust prevention, detection, and continuous improvement. Key Responsibilities Strategy & Governance: Define the global Quality Management System (QMS), policies, and KPIs (FPY, DPPM, RMA rate, audit scores). Standardize across sites and suppliers. Customer Quality: Own customer quality interface; lead executive reviews; align on quality agreements and purge/replacement plans; oversee PCNs and SQE engagement. NPI Quality: Embed APQP/PPAP, CTQs, and gated readiness in new programs; drive process capability (Cp/Cpk), measurement systems (MSA), and qualification (DQ/IQ/OQ/PQ). Manufacturing Quality: Deploy SPC, layered process audits, mistake-proofing, and rapid containment; run weekly global quality reviews; ensure compliance to regulatory/industry standards. Problem Solving: Institutionalize 8D root cause and corrective action; lead cross-functional FA on top issues. Supplier Quality: Set SQE/PPM targets; qualify second sources; manage incoming quality and change control (PCNs). Digital Quality: Scale AI vision and analytics playbooks for in-factory reliability and inline detection; build dashboards for real-time quality health. People & Culture: Build and mentor a high-performing global quality team; develop succession and training (SPC, 8D, MSA, FMEA). Qualifications: BS in Engineering (EE/ME/IE) required; MS/MBA preferred. 10-15+ years in Quality leadership across multi-site, high-mix electronics manufacturing (connectors/cables/EMS/semiconductor adjacent). Deep expertise in APQP, PPAP, SPC, MSA, FMEA, DOE, reliability and FA (metrology, microscopy, environmental/electrical tests). Proven track record with Tier-1 customers and ramp/scale scenarios; strong program and stakeholder management. Ability to travel globally (25-40%).

Quality Manager / Quality Lead / Head of Quality required to join a world leading Industrial engineering manufacturer. The successful Quality Manager / Quality Lead / Head of Quality will lead and deliver manufacturing quality processes in line with current ISO standards with the ambition to introduce automotive grade ISO standards. The successful Quality Manager / Quality Lead / Head of Quality will have Quality management or Quality lead experience within industrial engineering manufacturing. For example, filtration, automotive, aerospace, industrial materials, power transmission, fluid power, oil & gas, food & bev, and or similar fast paced engineering manufacturing environments. The manufacturing site is commutable from the following - Dover, Rochester, Portsmouth, Manchester, Portland. Package $130,000- $135,000 20% Bonus 401k Further benefits - company allowances Quality Manager / Quality Lead / Head of Quality Role Will lead and deliver manufacturing quality processes in line with current ISO standards with the ambition to introduce automotive grade ISO standards. Drive continuous improvement with a focus on product reliability, defect detection and customer satisfaction. Oversee all quality activities, for example - product inspection, customer complaints, final inspections. Manage internal and external audits in line with current ISO regulations. Serve as the primary point of contact for customers on quality-related matters; manage customer complaints, provide timely responses, and strengthen long-term relationships. Lead efforts to move toward automotive quality standards such as APQP, PPAP, IATF) Liaise with various engineering departments. Quality Manager / Quality Lead / Head of Quality Requirements Experience as a Quality Manager, Senior Quality Engineer, Quality Lead, Head of Quality, Quality Assurance Manager, Compliance & Quality Manager, QA Manager, QA/QC Manager, Quality Control Manager or similar within an Engineering Manufacturing environment. Proven quality management experience within a manufacturing environment, demonstrating QMS performance and customer service outcomes Strong knowledge and understanding of ISO quality systems, and experience of leading internal and external audits. Have a desire to move toward automotive standard quality procedures - experience with APQP, PPAP, IATF 16949 is highly desirable A technical mechanical, manufacturing, chemical engineering, science or similar qualification would be advantageous. Full clean driving license. Willingness to commute or relocate to the manufacturing site near Dover, New Hampshire.

75 Plumb Pak Drive, Winchester, New Hampshire 03470 United States of America **Why Oatey?** Since 1916, Oatey has provided reliable, high-quality products for the residential and commercial plumbing industries, with a commitment to delivering quality, building trust and improving lives. Today, Oatey operates a comprehensive manufacturing and distribution network comprised of industry leading family of companies: Oatey, Cherne, Keeney, Quick Drain, Hercules, Dearborn, GF Thompson, William H. Harvey, Masters, Contact, Belanger, Lansas, and Durgo. At Oatey, we're doing big things - and by joining us, you'll have the chance to do big things too. You can build a strong career in an innovative, inclusive, high-performance environment, with the confidence that your company cares - about you, our customers and our world. **Ready to make an impact in a place where you matter?** - **Position Summary:** Ensures the quality of all processes, procedures, materials, processes rework and finished products. Also performs scheduled tasks as support for environmental and safety functions with additional responsibilities as assigned. This position is a second shift 3:00PM-11:30PM Monday-Friday work schedule and reports directly to Quality Manager. **Position Responsibilities:** Conduct daily quality inspections in all departments to audit the following: Procedure compliance/documentation with ISO9001 quality systems. In-process quality inspections, using established procedures. Incoming inspection, including first piece inspection, verification of Supplier's Certificates of Analysis, etc. Validation of product quality conformance to specifications. Complete ongoing Reliability Testing to ensure current products continue to meet product performance and/or formulation specs. Provide disposition and segregation of rejected materials and/or products. Summarize data and provide appropriate reports. Maintains rework inventory. Provides samples and sample data. Maintain calibration/verification records for all lab testing instrumentation and hand-held devices. Prepare test pipes (go-no go Gauges) for fit testing. Supply manufacturing with calibrated measuring and test equipment. Provide organizational quality support by assisting with problem resolution on the shop floor which includes gathering information on any quality-related issues, conducting root cause analysis and providing resolution for non-conformities. Participate in manufacturing CIP meetings as the QA representative and in ongoing quality training of manufacturing and QA staff. Maintain good housekeeping in lab, office and storage areas. Maintain and keep organized all QA files and documentation for easy reference and ISO9001 documentation compliance. Other duties as assigned. **Knowledge and Experience** Good communication and organizational skills. Computer literacy with Microsoft Office software applications. Excellent problem-solving and analytical skills. Basic understanding of quality concepts including variation, process control and root cause analysis. Cooperative attitude toward co-workers and supervisors. Knowledge of various equipment used in a laboratory (Fill machines, pallet jack, box knife, batch gun, mix tanks, drum mover, microscope, viscometer, Gas Chromatograph, and computer). **Education and Certification** High School Diploma required. Associate's Degree in a business, engineering or scientific course of study or equivalent experience in a manufacturing or laboratory environment preferred. At Oatey we are committed to help our Associates grow their career. Apply today and grow with Oatey!

Job Posting Start Date 12-11-2025 Job Posting End DateFlex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world.A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.Job Summary Farm, a Flex company with over 50 years of experience in providing award-winning development services for medical, life sciences, and consumer healthcare sectors, is seeking a Supplier Qualtiy Engineer in Hollis, NH. The Supplier Quality Engineer is responsible for supporting supplier-related activities on development teams at Farm. He or she ensures that the development team is compliant with the policies and procedures of Farm's quality management system (QMS). The Supplier Quality Engineer receives direction from the Director of Quality and input from Program Managers and program team members. What a typical day looks like: Support product development as an embedded program team member working alongside program managers, researchers, human factors engineers, designers, mechanical engineers, electrical engineers and process engineers. Facilitate selection of suppliers to support late-stage development and clinical builds. Qualify suppliers via capability questionnaires, risk assessment, supplier file creation/management and remote or on-site audits. Represent program team supplier quality requirements during collaboration with procurement and supply chain resources. Develop program supplier and incoming inspection plans for late-stage development and clinical builds based on input from program managers, engineers, suppliers and customers. Plan and support test method and process validation activities completed by suppliers. Complete incoming inspection and management of materials for late-stage development and clinical builds. Manage site non-conforming material review process. Lead supplier-related corrective action and preventive action resolution. Manage site quality management system approved supplier list, supplier files and supplier performance metrics. Establish, evaluate, qualify, encourage use of and continuous improvement to supplier management processes, procedures and standard tools used by program teams. Participate in internal, customer and notified body audits of the quality management system. Interacts with customers, suppliers and external auditors to develop close working relationships. Participates in customer strategy meetings and discussions regarding the development of program quality requirements and plans. Participates in the technical review process on development programs. The experience we're looking to add to our team, Bachelor's degree in engineering, science, or equivalent technical discipline 1+ years of supplier quality experience Analytical thinking, plus verbal and technical writing skills Demonstrated team collaboration experience Previous medical device industry experience/ ISO13485 (prefer) What you'll receive for the great work you provide: Full range of medical, dental, and vision plans Life Insurance Short-term and Long-term Disability Matching 401(k) Contributions Vacation and Paid Sick Time Tuition Reimbursement Job CategoryQualityRelocation: Eligible for domestic relocation only Is Sponsorship Available? NoFlex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).

The Quality Coordinator will work in the Internal Quality Team on military/ aerospace products. The position will be responsible for activities that effectively identify, manage and report status of products and compliance with applicable regulatory requirements in the Aerospace/Defense Industries. The Quality Coordinator will be assisting the quality team in retrieving all proper documentation needed before product goes to production. This position reports directly to the Quality Supervisor From time to time assist in stockroom with kitting/cut verification of cables Preform inspections of documents in the production area, being sure they are at the required revision levels and ensuring paperwork is filled out correctly and completely Assist the quality team with incoming inspections, documenting per procedure Requirements This is an onsite position Knowledge and experience of various computer applications Detail oriented Must be a US person for US Department of Defense work Familiarity of AS9100 and ISO9000:2001 a plus Attention to detail and asking ‘why' is required Familiar with Military or Medical products/procedures a plus High School Diploma required Technical training in or knowledge of fiber optics a plus Fluency in English (verbal and written). PM19

Your Career Begins at Timken If you're ready for a challenging career that provides you with the ability to advance personally and professionally, look to Timken. Our associates make the world more productive by improving the efficiency and reliability of the machinery that keeps industry in motion. What We Offer: Competitive Pay Comprehensive benefits package, including medical, dental and vision coverage. Benefits start on first day of employment. 401(k) retirement savings plan with generous company match 10 paid holidays per year plus paid vacation. Paid parental leave at one year of service. Employee discounts on products and services. Education expense reimbursement, eligible to apply at first day of employment. Opportunities for professional development and career growth. Position Summary: The Quality Manager should have a diverse knowledge of super precision ball bearings, familiarity with Aerospace and DOD applications a plus, and a diverse knowledge of the unique specifications and gauging methods for each type of product to ensure compliance to Timken and customer specific requirements. The manager should have some background with CMM gaging and experience applying this technology and programming in a job shop environment with over 7000 SKU's. The Quality Manager is responsible for the plant's quality management system (QMS) and associated metrology equipment for the plant. Essential Responsibilities: Customer Satisfaction: Accountable for establishing the system for product quality appraisals in the manufacturing process to meet internal specifications and global customer expectations. Must communicate with internal sales and service engineers as they interface with customers. Responsible for responding to customer complaints in a timely manner. Manage rework operations and required customer documentation. Possess general manufacturing and application knowledge of miniature precision ball bearings. Coordinates customer PPAPs & FAI's. Manage all product and process audits to ensure compliance, including customer audits, internal quality audits, and outgoing quality audits. Quality Management System: Responsible for attaining and maintaining quality certifications and communicating with the 3rd party registrar. This includes NADCAP and AS9100 certifications. Responsible for maintaining all metrology methods and calibrations. Responsible for the metallurgical integrity of the plant's heat treat process, including quality systems concerning product metallurgy. Responsible for implementing and maintaining all aspects of the Timken Quality Management System (TQMS) and implementing the modules as required. Supplier Quality Responsible for assuring incoming product quality. Works with corporate Supplier Development to assure suppliers maintain a quality system and proper controls during the manufactuing of the product. Works with corporate Supplier Development to resolve quality issues/complaints with suppliers, while balancing the risk to our customers and to the supply chain. Continuous Improvement Manage and direct quality related continuous improvement to reduce scrap and lower operations costs. Coordinates machine and gaging capability studies while making recommendations for continuous improvement as a result of these studies Metrology Responsible for maintenance, certification, calibration, and availability of all CMMs, “hard” gauges, electronic gauges and product masters required. General Responsibilities Responsible for the training and development of team members in the Quality Dept. Lead Management team in review of plant quality metrics and promote the use of disciplined problem-solving techniques and corrective action to drive continuous improvement in all areas of the plant Basic Qualifications: Bachelor's degree in engineering, materials, management or another technical field Minimum 3-5 years' experience in a manufacturing environment Experience developing and maintaining quality management systems - including metrology and SPC. Excellent written and oral communication skills. Experience interacting with suppliers and customers. Excellent computer skills and ability to analyze data. Preferred Qualifications: ASQ: Certified Quality Engineer, Certified Quality Auditor and/or Certified Quality Manager Masters Degree Shainin or Six-Sigma Certification. Experience in project management. Experience managing a QMS. Experience in metal working - including machining, heat treating, grinding, and assembly. Experience with quality systems in a NADCAP and/or AS9100 certified plan. Location: Timken, Keene, NH Job Type: Full-Time Shift: Day Shift Salary Range: $98,000.00- $140,000.00 All qualified applicants shall be treated equally according to their individual qualifications, abilities, experiences and other employment standards. There will be no discrimination due to gender or gender identity, race, religion, color, national origin, ancestry, age, disability, sexual orientation, veteran/military status or any other basis protected by applicable law.

At Spartronics, every product we build has a purpose - and lives depend on the quality behind it. As a leading Electronic Manufacturing Services (EMS) provider, we partner with top innovators in the medical device, life sciences, aerospace, defense, and industrial markets to deliver electronics that perform flawlessly when it matters most. Our mission is simple but powerful: to be the preferred provider of fail-safe electronic solutions that save lives and protect what matters most. As a Quality Manager in Plaistow, NH, you'll play a critical role in advancing that mission by ensuring the quality, compliance, and reliability of the products we produce. You'll apply your technical expertise and problem-solving skills to maintain the highest standards of excellence - from product design and validation to continuous process improvement. Your leadership and insight help ensure that every product we deliver supports patient safety and improves lives around the world. Position: Quality Manager On-Site Work- Manufacturing Plant Location: Plaistow, NH As a Quality Manager at Spartronics, you'll play a pivotal role in the development and implementation of Quality Procedures in compliance with AS9100/ISO 9001:2015. What a Typical Day Looks Like: Maintain our Quality Management System Documentation to ensure compliance to AS9100D/ISO 9001:2015 requirements. Own our Quality Management Systems (QMS) and drive all operations in parallel with standards and practices conducive to a successfully run QMS. Lead all QMS activities, Internal audits, External audits, Management Review. Manage our Shelf Life, Calibration, and Layered Process Audit Programs. Lead root cause analysis and implement corrective and preventive actions (CAPA) for defects and customer complaints. Support flow-down of defense-specific requirements (e.g., ITAR, counterfeit parts prevention, special process control, PPAPs) through supplier documentation and quality plans. Drive all daily activities to ensure consistent development of new programs moving into manufacturing. Plan and direct research to recommend improvement or expansion of systems and/or operations. Establish and maintain satisfactory customer and public relations, through direct or delegated contacts with representative individuals and groups. Lead plant in error-proofing and detection improvement initiatives. Lead plant in APQP plan development, review, and sustainment. Coach plant teams in effective customer complaint, problem solving, and verification activities. Ensure that quality engineering effectively interprets and flows down customer contractual quality requirements to programs, engineering, supply chain, manufacturing, and inspection. Must interface successfully with vendors, external and internal customers by discussing quality specifications and actions taken to prevent or correct problems with products produced and post-delivery defects. Oversee and ensure the success of quality engineers who review engineering and manufacturing information, specifications and bills of materials; production, tool and test equipment drawings; production and tool plans; operations and routing sheets: production, storage and shipping methods to assure that products meet customers' requirements with minimum variation and ease of inspection. Ensure generation of quality metrics & trend charts and other reports, which indicate the quality of the items produced. Analyze these reports to determine correct trends. Lead and manage teams that perform investigations to determine the root cause for product and process non-conformances. Ensure that quality engineering initiates along with inspection and test methods/procedures comply with all quality and regulatory requirements. Assist in cost reduction through efficient planning, early detection of production errors and utilization of inspection techniques. Support Lean implementation in the facility Carry out leadership/management responsibilities in accordance with the organization's policies and applicable laws. Responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems. Support on-going operations as needed. Requirements The experience we're looking for to add to the team: Proven ability to deliver continuous improvement in quality, delivery, and cost (QDC) in manufacturing engineering process improvement projects. Relevant Quality experience gained within an Aerospace Engineering or Manufacturing Environment, and proven knowledge of Quality processes. Excellent written and verbal communication skills with a strong customer focus. Experience with CAPA (Corrective and Preventive Action) systems. Strong influencer with the ability to drive a step change in approach to quality assurance. Ability to build strong relationships with both internal stakeholders and external customers. Must have working knowledge of AS9100 procedural documentation requirements and AS9102 First Article Inspection requirements to ensure adherence to contract-specific quality clauses, first article inspection (FAI) requirements (AS9102), and material traceability. Bachelor's Degree in Engineering or equivalent, strongly preferred or related field with progressive experience in manufacturing or other job related experience deemed acceptable by the hiring team. Have a successful track record in building and supporting cross functional teams with Operations and Program Management. Ability to thrive in a high-paced, ever-changing manufacturing environment with a proactive and solutions-oriented mindset. Experience in electronics manufacturing, contract manufacturing, or a similar environment. Minimum of 5-7 years of Quality Management experience. Excellent analytical skills using Six Sigma and Lean Principles. Proven leadership skills. Ability to function effectively in a team environment. Previous departmental management experience managing an engineering group with demonstrated ability to manage multiple projects simultaneously using formal project planning techniques. Due to ITAR regulations, you must be a US Citizen, Permanent Resident, or Green Card Holder. We can not sponsor Visas. Our Commitment: At Spartronics, we're dedicated to fostering an inclusive, diverse, and equitable workplace. We believe that diverse perspectives drive innovation, and we welcome candidates of all backgrounds to apply. Our culture at Spartronics values accountability, unity, respect, and transparency. These winning values are the lifeblood of our business. We embrace diversity through people who believe in these values. Embracing our employees' differences enables us to be a stronger team. Join Our Journey: If you're ready to be a part of something extraordinary, challenge the status quo, and shape the future, then we want to hear from you. Together, we'll continue to win, while we build products lives depend on. Our Benefits: Full range of medical, dental, and vision benefits. Flexible Savings Accounts for Medical, Dependent Care, and Limited Purpose (dental and vision only) PTO and Holiday Pay Company-paid life insurance and disability at 1 times your annual salary at no cost to you, with options to increase coverage amounts 401k with a company match of 50% to every dollar up to 6% Accident, Critical Illness, Hospital Indemnity, and Legal Insurance optional plans Employee Assistance Program Tuition Reimbursement Opportunities to grow and excel in the Electronics Manufacturing industry at a company that values promotions and learning from within. Every day is different, challenging, and rewarding. How to Apply: If this sounds like the perfect opportunity for you, please apply with your resume and a cover letter outlining your qualifications and why you're excited about joining Spartronics. Spartronics is an equal opportunity Employer/Veteran/Disabled 41 CFR 60-1.4. This position requires use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee.

Job Description Global Quality Manager (CBS) Location: Nashua,with periodic travel to manufacturing sites (e.g., Valley Green, Nashua, Mexicali, Nantong, Hanoi) Amphenol Cable Backplane Systems (CBS) operates at anextreme pace with rapid growth, driven by the global AI hardware infrastructure expansion. As theleading supplier of complex cabled backplane systems, CBS enables next-generation data center performance for technology titans. Our solutions involvethousands of twin-ax subassembliespackaged into custom mechanical assemblies withtightly controlled electrical and mechanical specifications. CBS supports customers fromearly concept development through full-scale datacenter deployment, ensuring reliability and precision at every stage. The CBS team is looking for a Global Quality Manager. The Global Quality Manager will lead the end-to-end global Quality strategy for Cable Backplane Systems (CBS), ensuring product and process quality across NPI and volume manufacturing, driving customer satisfaction, and reducing field returns through robust prevention, detection, and continuous improvement. Key Responsibilities Strategy & Governance: Define the global Quality Management System (QMS), policies, and KPIs (FPY, DPPM, RMA rate, audit scores). Standardize across sites and suppliers. Customer Quality: Own customer quality interface; lead executive reviews; align on quality agreements and purge/replacement plans; oversee PCNs and SQE engagement. NPI Quality: Embed APQP/PPAP, CTQs, and gated readiness in new programs; drive process capability (Cp/Cpk), measurement systems (MSA), and qualification (DQ/IQ/OQ/PQ). Manufacturing Quality: Deploy SPC, layered process audits, mistake-proofing, and rapid containment; run weekly global quality reviews; ensure compliance to regulatory/industry standards. Problem Solving: Institutionalize 8D root cause and corrective action; lead cross-functional FA on top issues. Supplier Quality: Set SQE/PPM targets; qualify second sources; manage incoming quality and change control (PCNs). Digital Quality: Scale AI vision and analytics playbooks for in-factory reliability and inline detection; build dashboards for real-time quality health. People & Culture: Build and mentor a high-performing global quality team; develop succession and training (SPC, 8D, MSA, FMEA). Qualifications: BS in Engineering (EE/ME/IE) required; MS/MBA preferred. 1015+ years in Quality leadership across multi-site, high-mix electronics manufacturing (connectors/cables/EMS/semiconductor adjacent). Deep expertise in APQP, PPAP, SPC, MSA, FMEA, DOE, reliability and FA (metrology, microscopy, environmental/electrical tests). Proven track record with Tier-1 customers and ramp/scale scenarios; strong program and stakeholder management. Ability to travel globally (2540%).

Job Requirements Why work for us? Alkegen brings together two of the world's leading specialty materials companies to create one new, innovation-driven leader focused on battery technologies, filtration media, and specialty insulation and sealing materials. Through global reach and breakthrough inventions, we're delivering products that enable the world to breathe easier, live greener, and go further than ever before. With over 60 manufacturing facilities with a global workforce of over 9,000 of the industry's most experienced talent, including insulation and filtration experts, Alkegen is uniquely positioned to help customers impact the environment in meaningful ways. Alkegen offers a range of dynamic career opportunities with globe-spanning reach. From production operators to engineers, technicians to specialists, sales to leadership, we're always looking for top talent ready to bring their best. Come grow with us. Responsibilities: Responsible for maintaining the ISO 9001: Quality Management System. Lead and conduct the annual Management Review Meeting Responsible for the Corrective Action / Preventive Action reports Promotes quality achievements and performance improvement throughout the plant and organization. Collaborates with R&D Department, Production personnel, and QC Lab operators in the evaluation of Customer returns materials (RGAs) Perform root cause analysis Assist Purchasing Department in Supplier Evaluations and submits Customer Questionnaire Visit customer's facilities to sort material and serve as a Liaison between the Company and the Customer's Quality Control Department as needed. Review and approve Plant Work Orders for release and work with Sales Department in the submittal of Concession requests Reclassify Plant Work Order and/or Nonconformance product as deemed necessary Aids Production and Finishing department in the resolution and disposition of nonconforming product Coaches and develops Quality team Assist HR in the creation and revision of all Company job descriptions and provide training Serve as a liaison for Customer audits and maintain awareness of Customer-specific product specifications Oversees all ISO 9001: internal audits Conducts monthly Quality Control meetings to review quality objectives and in-process performance quality metrics. Technical writing of company procedures, work instructions, forms and production reports Perform capability studies for R&D / Technical Services Exhibits a positive attitude that reflects upon the SFC team Supports and implements policies/procedures, including the Quality Management System. Performs projects or assignments as directed by the Plant Manager Qualifications/ Experience Bachelor Degree in Engineering or related field 10+ Year in Quality Control / Manufacturing and Management Expert in ISO 9001 Quality System Provide functional, technical and process leadership Excellent problems solving skills Excellent interpersonal savvy Demonstrated good leadership skills High level of attention to detail Strong Customer Service skills Strong focus on driving results Excellent interpersonal skills Ability to work as a team and indepentently Strong focus on training and developing talent Be a high-level performance Manager. IATF Preferred If you are interested in being part of a world class function here at Alkegen then we would love to hear from you. At Alkegen, we strive every day to help people - ALL PEOPLE - breathe easier, live greener and go further than ever before. We believe that diversity and inclusion is central to this mission and to our impact. Our diverse and inclusive culture drives our growth & innovation and we nurture it by actively embracing our differences and using our varied perspectives to solve the complex challenges facing our changing and diverse world. Employment selection and related decisions are made without regard to sex, race, ethnicity, nation of origin, religion, color, gender identity and expression, age, disability, education, opinions, culture, languages spoken, veteran's status, or any other protected class.

The Quality Assurance (QA) Manager is responsible for overseeing and ensuring the quality of all electronic products manufactured by the company. This role will involve managing the quality assurance team, developing and implementing quality management systems, and ensuring that all products meet both internal and external standards, including customer requirements and regulatory guidelines. Key Responsibilities: * Quality Management System (QMS): * Develop, implement, and maintain the company's quality assurance and control policies and procedures to ensure compliance with industry standards, such as ISO 9001, IPC, or others as applicable. * Continuously improve the QMS, ensuring it aligns with company goals and industry best practices. * Team Leadership and Development: * Lead and manage the quality assurance team, ensuring effective communication, collaboration, with all departments. * Provide training and mentorship to QA technicians to improve their technical skills and enhance team capabilities. * Assign and manage work tasks, setting goals, tracking performance, and providing ongoing feedback. * Product Testing & Validation: * Oversee the testing and validation of electronic components and finished products to ensure compliance with specifications, standards, and regulations at incoming. * Collaborate with engineering, R&D, and production teams to identify issues and root causes of quality failures and to ensure that corrective actions are taken. * Process Improvement: * Analyze data from testing and quality control reports to identify areas for process improvement. * Implement process changes that increase efficiency, reduce defects, and enhance the product quality. * Lead continuous improvement initiatives. * Supplier Quality Management: * Evaluate and approve suppliers/vendors based on their ability to meet quality standards. * Develop and maintain strong relationships with suppliers to ensure product quality and resolve any quality-related issues with supplied materials or components. * Work closely with suppliers to develop corrective actions when necessary. * Regulatory Compliance: * Ensure (where applicable) products meet regulatory and safety standards, such as UL, RoHS, etc. * Stay up to date with industry standards, regulations, and best practices related to quality assurance in electronics. * Root Cause Analysis & Corrective Actions: * Lead investigations into customer complaints, returns, or internal product failures to determine root causes. * Develop and implement corrective actions to prevent recurrence, documenting findings and improvement actions. * Reporting & Documentation: * Prepare and present detailed quality assurance reports for management, highlighting product quality trends, defects, improvements, and the status of corrective actions. * Maintain comprehensive records of quality control tests, audits, and reports to ensure compliance with internal and external audit requirements. #ConRes # of Hires Needed 1 Exemption Type Exempt Hiring Manager Job Requirements Qualifications: * Education: * Degree in Engineering or equivalent experience * Experience: * Minimum of 3-5 years of experience in Manufacturing/Production Engineering experience * Hands-on experience with electronic product testing and validation. * Strong knowledge of quality management systems (ISO 9001, IPC, etc.) and industry standards. * Skills: * Strong analytical and problem-solving skills. * Excellent communication and leadership abilities. * Skilled with quality management tools, such as SPC (Statistical Process Control), FMEA (Failure Mode Effects Analysis), and root cause analysis techniques. Key Competencies: * Attention to Detail: Ensures every product meets quality standards and customer expectations. * Problem-Solving: Identifies issues in the production process and develops effective solutions. * Communication: Clearly communicates quality expectations, performance metrics, and corrective actions to all team members and stakeholders. * Adaptability: Willing to continuously learn new techniques, tools, and technologies in the rapidly evolving electronics industry. Working Conditions: * Office-based with occasional travel to supplier sites. * May require some weekend or evening hours based on project deadlines or urgent issues.

Job Description Job Title: Quality Manager (Onsite Only) Department: Quality Reports To: President The Quality Manager is responsible for providing leadership, strategic direction, and oversight for all quality-related activities within Janco Electronics. This role ensures that the organization's products, processes, and systems meet or exceed customer, regulatory, and industry standards. The Quality Manager serves as the ISO Management Representative, maintaining compliance and continuous improvement across all facets of the Quality Management System (QMS). Essential Duties and Responsibilities: The Quality Manager's responsibilities include, but are not limited to: Provide direction and leadership to the Janco Electronics quality organization. Serve as the ISO Management Representative for the organization. Maintain, enhance, and ensure compliance with ISO 13485 (and other applicable standards such as ISO 9001). Plan and execute the internal audit program; internal auditing certification required. Manage supplier quality, including supplier qualification, approval, and ongoing performance ratings. Oversee and track Corrective Action / Preventive Action (CAPA) activities to ensure timely resolution and root cause elimination. Review, investigate, and respond to customer complaints, ensuring effective containment and corrective measures. Participate in and lead Material Review Board (MRB) processes to evaluate and disposition nonconforming materials. Administer and maintain the calibration system. Establish, maintain, and improve manufacturing quality procedures. Administer and maintain the Document Control System. Oversee and support the Employee Training Coordinator to ensure personnel are trained and competent in quality standards and procedures. Lead continuous improvement initiatives using data-driven methodologies such as root cause analysis, SPC, and lean manufacturing tools. Act as the primary point of contact for quality audits-customer, regulatory, and certification. Qualifications and Requirements: Education and Experience: Minimum of 5 years of quality experience within the Electronics Manufacturing Services (EMS) industry or related field. Bachelor's degree in Engineering, Quality Management, or a related discipline preferred; equivalent experience considered. Demonstrated experience managing ISO 13485 or ISO 9001 systems. Proven track record of leading quality teams in a manufacturing environment. Certifications: Internal Auditor Certification (required). ASQ Certification preferred. Knowledge, Skills, and Abilities: Strong understanding of quality tools and methodologies (8D, FMEA, SPC, CAPA, etc.). Knowledge of IPC standards and electronic assembly processes preferred. Excellent communication, leadership, and interpersonal skills. Proficient in Microsoft Office and quality management software systems. Detail-oriented with strong analytical and problem-solving skills. 8am - 5pm Monday through Friday

Reads and interprets work instructions, blueprints, and customer and industry specifications and requirements to determine dimensions, tolerances, and requirements. Completes source inspection tasks as assigned. Provides support for quality projects dictated by the Quality Leadership. Supports and completes activities concerned with development, application, and maintenance of quality standards, requirements, documents, and instructions for industrial processes, materials, and products. ESSENTIAL FUNCTIONS AND RESPONSIBILITIES Included are the following: Other duties may be assigned. Reviews contracts, blueprints, and customer/industry specifications to determine dimensions, tolerances and any other applicable inspection and test criteria or requirements. Interpret and apply U.S. Navy specifications, MIL-STD, NAVSEA requirements, and contractual quality clauses. Ensure compliance with DFARS and ITAR regulations. May develop, perform and initiate standards and methods for inspection, testing, and evaluation for machined, welded, and fabricated parts. These standards and methods may include but are not limited to Inspection Reports, Process Improvement (PI), CSI / GSI, DMR / MRB, and internal / external audits. Reviews documents and records to assist and support final inspection, customer source inspection, government source inspection, etc. Provides assistance and training to lower skilled inspectors and workers. Supports the developments of procedures, instructions, and forms for recording, evaluating, and reporting quality related information in the Quality Management System. May support programs to evaluate precision and accuracy of production equipment and testing, measurement, and analytical equipment and facilities. Supports and implements methods and procedures for disposition of discrepant material and devises methods to assess cost and responsibility. Assist and support in the DMR and MRB process. Supports and conducts internal and external (supplier) audits. May compile and write training material and conduct training sessions on quality control activities. Advanced skills in Word and Excel. Strong technical writing skills: ability to create or update procedures and work instructions. Analyze quality data to develop meaningful metrics. Lead or support continuous improvement initiatives to reduce defects and improve processes. Demonstrates responsibility and accountability for creating a professional, safe, and clean environment evidenced by being at work on time to perform assigned duties, following the policies of Granite State Manufacturing, always wearing safety glasses in designated areas, maintaining a neat and orderly work area, and following safety practices to prevent errors. Demonstrates commitment to teamwork by establishing effective relationships and networks with both managers/directors and workers and collaborating with them to accomplish shared purposes and goals. Abides by GSM Code of Ethics and Business Conduct standards and strictly observes all U.S. and foreign laws and regulations. Completes other duties assigned by Quality Leadership. Requirements QUALIFICATIONS, SKILLS, AND ABILITIES Four-year degree in Engineering or related field (Mechanical, Industrial, or Manufacturing preferred) from college or technical school; or ASQ Certified Quality Engineer; or five years of related experience and/or training or equivalent combination of education and experience. Advanced knowledge of inspection, special processes, and raw materials a plus. Extensive experience with root cause analysis and corrective action. Good meeting facilitation skills. Should know how to interpret Geometric Dimensioning & Tolerance. Should be knowledgeable with CMM, height gages, inspection tools and equipment, etc. Must be able to work independently without supervision. Must have the ability to work as team player in a group or team environment. Preference for experience in aerospace, defense, other regulated manufacturing environments; experience working with NAVSEA (submarines) is highly desirable. Experience in a machine shop or welding fabrication shop. BENEFICIAL SKILL OR EXPERIENCE Experience in programming, operating and setting up CMM's and Faro arms is beneficial but not required. Advanced knowledge of inspection, plating and coating processes, and raw materials a plus. A personal and professional background sufficient to secure a Government Security Clearance. Experience with M1 ERP system. AAP/EEO STATEMENT Granite State Manufacturing (GSM) is an equal opportunity employer. GSM does not discriminate on the basis of race, color, religion, sex, gender, gender identity or expression, national origin, citizenship, veteran status, age, physical or mental disability, genetic information, marital status, sexual orientation, or any other consideration made unlawful by applicable federal, state, or local laws in its programs, activities, or employment. Benefits Paid time off Floating holidays Paid holidays 401(k) 401(k) company matching Dental & Vision insurance (Company paid) Employee assistance program Flexible spending account Competitive health insurance Health savings account Life insurance Referral program

**Collaborate with Innovative 3Mers Around the World** Choosing where to start and grow your career has a major impact on your professional and personal life, so it's equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With a diversity of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, creative 3Mers. **This position provides an opportunity to transition from other private, public, government or military experience to a 3M career.** **The Impact You'll Make in this Role** As a Quality Technician, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative people around the world. Here, you will make an impact by: + Support product quality, product development, process scale-ups, and production processes by performing standardized, specialized, or complex tests, measurements, and tasks on experimental or standard production. + Activities will focus on the appraisal of raw materials, semi-finished, and finished goods. + Ensures that 3M quality standards and procedures are met and maintained. + Teach plant personnel quality methods and measurement techniques. + Complete daily audits of the manufacturing floor, quantify and report the results. Run precision test equipment and report results. + Other quality related tasks as required. **Your Skills and Expertise** To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications: + High school diploma/GED or higher (completed and verified prior to start) from an accredited institution + One (1) year combined quality and/or laboratory experience in a private, public, government or military environment + One (1) year experience utilizing Microsoft Office (including Excel) Additional qualifications that could help you succeed even further in this role include: + Associates/Two Year Technical degree or higher from an accredited institution in a private, public, government or military environment + Three (3) years combined quality and/or laboratory experience + Equipment validation experience + Good written and verbal communication skills that include excellent data collection and management + Flexible and responsive to changing priorities; able to multi-task; good organizational skills; attention to detail and compliant behaviors **Work location:** + **On-site Tilton, NH 3rd Shift schedule** **Travel: May include up to 5% domestic/international** **Relocation Assistance: Is not authorized** **Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).** **Supporting Your Well-being** 3M offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope. **Chat with Max** For assistance with searching through our current job openings or for more information about all things 3M, visit Max, our virtual recruiting assistant on 3M.com/careers. Applicable to US Applicants Only:The expected compensation range for this position is $59,409 - $72,611, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate's relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: **************************************************************** Good Faith Posting Date Range 11/25/2025 To 12/25/2025 Or until filled All US-based 3M full time employees will need to sign an employee agreement as a condition of employment with 3M. This agreement lays out key terms on using 3M Confidential Information and Trade Secrets. It also has provisions discussing conflicts of interest and how inventions are assigned. Employees that are Job Grade 7 or equivalent and above may also have obligations to not compete against 3M or solicit its employees or customers, both during their employment, and for a period after they leave 3M. Learn more about 3M's creative solutions to the world's problems at ********** or on Instagram, Facebook, and LinkedIn @3M. Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties. Safety is a core value at 3M. All employees are expected to contribute to a strong Environmental Health and Safety (EHS) culture by following safety policies, identifying hazards, and engaging in continuous improvement. Pay & Benefits Overview: https://**********/3M/en\_US/careers-us/working-at-3m/benefits/ 3M does not discriminate in hiring or employment on the basis of race, color, sex, national origin, religion, age, disability, veteran status, or any other characteristic protected by applicable law. **Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.** **3M Global Terms of Use and Privacy Statement** Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at 3M are conditioned on your acceptance and compliance with these terms. Please access the linked document by clicking here (************************************************************************************************* , select the country where you are applying for employment, and review. Before submitting your application, you will be asked to confirm your agreement with the terms. At 3M we apply science in collaborative ways to improve lives daily as our employees connect with customers all around the world. Learn more about 3M's creative solutions to global challenges at ********** or on Twitter @3M or @3MNews. 3M does not discriminate in hiring or employment on the basis of race, color, sex, national origin, religion, age, disability, veteran status, or any other characteristic protected by applicable law.

Job Title: Quality Technician Pay: $22-$25 per hour, depending on experience Hours: Monday - Thursday, 6:00 AM - 2:30 PM, and a half day on Friday! 36 hours a week! As a Quality Technician, you'll help ensure that all customer and company quality standards are met-from raw materials to finished goods. You'll work closely with the Quality Manager and other team members to support inspections, documentation, and compliance activities that keep operations running smoothly. What You'll Do As a Quality Technician, you will be responsible for: Reviewing and approving testing reports from third-party laboratories Maintaining up-to-date knowledge of ASME regulations and applicable industry codes Receiving and inspecting returned products to determine quality and return category Evaluating inbound goods, preparing documentation, and managing return transactions Using metrology hand tools and small test fixtures to perform mechanical inspections Collaborating with the MRB team to determine the disposition of nonconforming materials Supporting company quality standards and 6S organization practices Working independently with minimal supervision Performing additional duties as assigned by the Quality Manager What You'll Bring The ideal candidate for this role will have: High school diploma or equivalent (technical education preferred) At least 5 years of experience in a similar quality technician or inspection role Strong math and mechanical aptitude Ability to read and interpret blueprints Familiarity with ASME Section II and IV (preferred) Proficiency with Microsoft Office and general computer use Experience with ERP systems such as M2K (inventory moves, RGA processing, etc.) Excellent communication, organization, and time management skills Ability to lift up to 35 pounds and work in a fast-paced environment Why Join Us in Rochester, NH? Stable schedule: Enjoy a four-and-a-half-day workweek with Fridays ending early Great pay: Competitive hourly rate based on experience Career opportunity: Temp-to-hire position with long-term potential Affordable health and prescription coverage with no waiting period Employer benefits available upon permanent hire Ask about our Referral Bonus Program to earn extra cash! Location & Schedule This position is on-site in Rochester, NH and follows a Monday-Thursday 6:00 AM-2:30 PM, Friday half-day schedule. 36/HRS a week! Ready to Take the Next Step? If you're ready to start a rewarding career as a Quality Technician in Rochester, NH, apply today or contact our recruiting team to learn more. Don't wait - we're hiring now!

Working at Freudenberg: We will wow your world! Responsibilities: Maintain Excellence: Support the surveillance and execution of the Global Management System (GMS) through internal audits, ensuring FST achieves excellence. Ensure Compliance: Effectively close non-conformities to protect FST and its customers, preventing recurring issues. Collaborate for Success: Work with various stakeholders to evaluate customer-specific requirements related to the Quality Management System and Warranty, ensuring legal compliance. Innovate Quality Strategies: Define and identify new quality strategies and system tools to support FST's sustainable success, especially when market requirements change or new business is acquired. Drive Continuous Improvement: Seek opportunities to enhance the Global Quality Management System, directly impacting FST's profitability. Monitor and Improve: Evaluate and analyze Quality Key Performance Indicators, guiding improvement projects to promptly react and avoid waste. Ensure Compliance: Execute internal system and process audits to confirm compliance with international standards and FST requirements, identifying best practices within the organization. Qualifications: Bachelor's Degree in Relevant Field; advanced degree preferred or compensating years of experience Specified Years of Industry-relevant professional experience Relevant certifications, system experience, and training Professional-Level English language skills preferred Communication & Collaboration: Communicates clearly and concisely, while engaging proactively with colleagues at all levels of the organization. Value for Customers: Anticipates, understands and meets internal/external customers' needs and expectations. Develops solutions based on a customer centric approach. Innovation: Drives and supports innovative ideas, while taking informed risks to seek and develop new or improved solutions. Drive & Execution: Proactively identifies what needs to be done and takes action. Explores new ways and pursues new opportunities. The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law. Freudenberg-NOK General Partnership

We are always looking forward to receiving resumes from candidates with skills and technical experience in the aerospace sector. We are very happy to receive speculative resumes if you are looking for a career change within the aerospace industry. Our flexible recruitment services will provide you with the following employment options: * Contract * Contract to Direct * Direct Our experienced consultants are experts in their field and are well placed to advise you on all aspects of aerospace recruitment opportunities, and employment trends.

**_What Application Development & Maintenance contributes to Cardinal Health_** Information Technology oversees the effective development, delivery, and operation of computing and information services. This function anticipates, plans, and delivers Information Technology solutions and strategies that enable operations and drive business value. Application Development & Maintenance performs configuration or coding to develop, enhance and sustain the organization's software systems in a cross-functional team environment through adherence to established design control processes and good engineering practices. This job family programs and configures end user applications, systems, databases and websites to achieve the organization's internal needs and externally-facing business needs. Application Development & Maintenance partners with business leaders, investigates user needs and conducts regular assessments, maintenance and enhancements of existing applications. The SAP Software Engineer focused on Data Conversions, Data Quality, and Reporting is responsible for designing, developing, and maintaining data solutions that ensure data integrity and enable effective business intelligence. The role combines technical skills in data migration and ETL processes with an understanding of data governance and reporting tools. **_What is expected of you and others at this level_** + Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects + May contribute to the development of policies and procedures + Works on complex projects of large scope + Develops technical solutions to a wide range of difficult problems + Solutions are innovative and consistent with organization objectives + Completes work; independently receives general guidance on new projects + Work reviewed for purpose of meeting objectives + May act as a mentor to less experienced colleagues **_Responsibilities_** + Design and execute data conversion strategies for SAP implementations and upgrades, including data extraction, transformation, and loading (ETL) from legacy systems into SAP. + Utilize SAP data migration tools such as SAP Data Services, LSMW, and Migration Cockpit to perform data loads and conversions. + Develop and maintain technical specifications, data mapping documents, and transformation rules. + Collaborate with business and technical teams to gather data requirements and ensure seamless data flow across systems. + Establish and maintain data quality frameworks to ensure the accuracy, consistency, and integrity of master and transactional data in SAP. + Perform data profiling, cleansing, and validation to identify and resolve data discrepancies before and after migration. + Define and monitor data quality metrics and key performance indicators (KPIs). + Work with business data stewards to correct data quality issues and promote data governance policies and standards. + Design, develop, and implement reporting solutions, dashboards, and analytical models using SAP technologies like SAP Analytics Cloud (SAC), SAP BW/4HANA, or SAP Fiori. + Translate business needs into technical specifications for reports and ad-hoc queries. + Optimize report performance and data extraction processes for efficiency. + Provide support and training to end-users on reporting tools to enable data-driven decision-making **_Qualifications_** + Bachelor's Degree in related field preferred or equivalent work experience preferred + Proven experience in SAP Data Conversions, migrations and ETL processes. + Proficiency with SAP data tools such as SAP Data Services, SAP BW/HANA or SAP Analytics Cloud + Strong knowledge of SQL, data modelling and database concepts + Experience with SAP modules and data structures (e.g., Master Data, Financials, Supply Chain, OTC, PTP processes). + Excellent analytical, problem solving and communication skills + Ability to work both independently and collaboratively with cross-functional teams **Anticipated salary range:** $94,900 - $135,600 **Bonus eligible:** No **Benefits:** Cardinal Health offers a wide variety of benefits and programs to support health and well-being. + Medical, dental and vision coverage + Paid time off plan + Health savings account (HSA) + 401k savings plan + Access to wages before pay day with my FlexPay + Flexible spending accounts (FSAs) + Short- and long-term disability coverage + Work-Life resources + Paid parental leave + Healthy lifestyle programs **Application window anticipated to close:** 01/20/2026 *if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity _Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._ _Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._ _To read and review this privacy notice click_ here (***************************************************************************************************************************

The Allegro team is united by a clear purpose-advancing technologies that make the world safer, more efficient, and more sustainable. With over 30 years of experience in semiconductor innovation, we bring that purpose to life across every part of the business-from breakthrough product development and customer success to how we show up for each other and the communities we serve. The Opportunity Develop robust and reliable packaging solutions for Allegro's cutting-edge sensor, power, and high-voltage power integrated circuits. Collaborate with cross-functional teams, including design, quality, reliability, and manufacturing, to ensure that package designs meet stringent performance, quality, and cost targets. Responsible for all aspects of package development, from initial concept and design through qualification, failure analysis, and high-volume production release. What You Will Do Design and develop integrated circuit packages, process flows, and materials supporting Sensor, Power, and High Voltage Power product development. Create AutoCAD drawings, 3D models, and detailed specifications for integrated circuit packages. Employ DFMEA and other Advanced Product Quality Process (APQP) methodologies to ensure designs meet project mission profiles and Allegro's quality and reliability objectives. Collaborate with the Allegro quality and reliability team to design appropriate qualification and failure analysis plans for new packages. Analyze qualification data and support the transition of new packages into high-volume production. Manage project schedules and deliverables and maintain design documents and reports in SharePoint. Collaborate with cross-functional teams on new package development and optimization of existing high-volume production packages. Work closely with internal and external package assembly sites to verify in-process data and oversee pre-production manufacturing execution. Perform modeling and simulation using ANSYS and LS-DYNA for various semiconductor packages and processes. Conduct mechanical and thermal material characterizations using an Instron mechanical tester and Siemens T3ster. Create detailed technical reports and presentations for both technical and non-technical audiences. Hybrid office/home work schedule. Requirements: Bachelor's degree in Electrical Engineering, Mechanical Engineering, Materials Science, or Industrial and Systems Engineering and 5 years of experience with: working with package design for magnetic sensing and power IC applications; and Using AutoCAD and SolidWorks, as well as ANSYS and LS-DYNA simulation platforms. Alternatively, will accept a Master's degree in the same fields and 3 years of same experience. As another alternative, will accept a Ph.D. in the same fields with specific coursework involving Materials Science and Engineering Fundamentals, including: Material Structure Analysis Metal Physics Solid State Physics Thermodynamics of Materials Fundamentals of Crystallography Why Allegro? Join Allegro and become part of a team where your contributions truly matter. We foster a culture of Real Innovation, empowering you to push boundaries, develop cutting-edge solutions, and drive continuous improvement. Your work will create a Real Impact by solving complex real-world challenges that fuel our success and shape the future of technology. You'll experience Real Connection, collaborating with talented colleagues around the globe in an environment built on trust, respect, and a shared purpose. Join us-and help build what's next. At Allegro, we are committed to providing a harassment-free environment of mutual respect to fuel innovation through inclusive thought collaboration. Allegro is an Equal Opportunity Employer and does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, physical or mental disability, national origin, veteran status, parental status, or any other basis covered by appropriate law. Allegro makes hiring decisions based solely on qualifications, merit, and business needs at the time. Eligible applicants must reside in a state where Allegro currently has an office location: This includes New Hampshire, Massachusetts, Texas, and Michigan. Certain positions (such as field sales roles) may be exempt from this requirement.

We are seeking a Manufacturing Engineer to drive process development, build execution, and the transition to scalable manufacturing for complex mechanical and electromechanical assemblies. This is a critical, cross-functional role that collaborates internally with engineering, supply chain, and operations teams, as well as externally with suppliers, partners, and customers. How You Will Make an Impact as a Manufacturing Engineer: Develop and maintain essential manufacturing documentation including Bills of Materials (BOMs), line layouts, assembly instructions, fixtures, pFMEAs, and production control methods. Plan, lead, and execute pre-production builds with a long-term vision for scalable, high-volume production. Collaborate closely with design and engineering teams to ensure products are robust, reliable, and ready for manufacturing. Consult with suppliers to define product specifications, and partner with the supply chain team to procure required equipment, materials, and parts. Interface with manufacturing partners throughout the design transfer process to ensure on-time delivery of high-quality products that meet all performance criteria. Skills you will need to be successful in this role: B.S. in Mechanical or Manufacturing Engineering with 2-5 years of experience, or A.S. degree with 3-6 years of experience. Strong candidates with less experience may be considered. Experience with electromechanical assembly and manufacturing process development. Working knowledge of Lean Manufacturing, Six Sigma, or green manufacturing principles is a plus. Proficiency in CAD software; SolidWorks preferred. Familiarity with ERP systems is a plus. Experience in medical device manufacturing is highly desirable. Proven ability to set up manufacturing assembly lines with an eye toward scalability and efficiency. Strong understanding of component forming processes, assembly operations, production line optimization, and design for manufacturability. Demonstrated passion for solving complex engineering problems and a curiosity for understanding how things work. Excellent communication, collaboration, and time management skills. About DEKA: One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age. Behind DEKA's brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.