Jobs at ISO New England Inc.

The Design Quality Engineer role supports Enovis's medical technology division by ensuring product safety, quality, and regulatory compliance throughout the design and manufacturing lifecycle. Key responsibilities include leading risk analysis through DFMEAs, authoring quality procedures and work instructions, and serving as a subject matter expert during ISO and FDA audits. The position also involves reviewing design documentation, managing nonconforming materials, and driving corrective actions for device failures. This opportunity appeals to candidates seeking to contribute to a mission-driven culture focused on improving patient outcomes through continuous innovation. The role offers a collaborative environment within a global organization, requiring minimal travel and providing a clean, professional office setting.

The Software Compliance Engineer role supports the Software Quality Assurance team within Abbott's Diabetes Care division in Alameda, California. This position ensures that medical device software and firmware meet strict regulatory standards, including FDA QSR and ISO guidelines. Key responsibilities include reviewing change plans and test reports to verify compliance, managing defect tracking processes, and serving as a subject matter expert during internal and external audits. The role involves active participation in Agile development cycles and collaboration with cross-functional engineering teams. This opportunity appeals to candidates seeking to contribute to life-changing healthcare technologies while working in a globally recognized company that values diversity and professional growth. The position requires occasional travel and is based at the Alameda facility.

This Risk Analyst role supports the Middle Office operations at Leeward Renewable Energy, a company building a sustainable American energy future through utility-scale wind, solar, and storage projects. The position involves building the risk management function by analyzing, modeling, and reporting market risk for energy and congestion trading activities. Key responsibilities include quantifying portfolio risk for traders, developing risk reports and models using tools like Excel and Python, and collaborating with finance, compliance, and trading teams to ensure regulatory adherence and operational efficiency. The role appeals to candidates seeking to contribute to a mission-driven organization with a culture of integrity and community impact. It offers a hybrid work arrangement and opportunities for professional growth within a robust pipeline of domestic energy projects.

This full-time Material Handler and Sorter role supports manufacturing operations at Jabil during the first shift, Monday through Thursday. The position focuses on accurately kitting materials for production lines, utilizing RF scanners to move items from the stockroom to build locations, and managing inventory transactions within company systems. Key responsibilities include organizing the kitting area according to 5S standards, ensuring precise part quantities for different component types, and maintaining detailed documentation for traceability and quality compliance. The role appeals to individuals seeking a stable position within a global engineering and supply chain leader known for its commitment to sustainability and diverse communities. The work environment emphasizes safety, adherence to ISO policies, and a collaborative atmosphere where employees contribute to efficient manufacturing processes.

The Quality Supervisor role leads the quality control inspection group within TAS Energy's manufacturing division in Houston. Key responsibilities include managing team performance and recruitment, overseeing budget and headcount planning, and implementing programs to enhance quality metrics and manufacturing efficiencies. The position requires interpreting complex engineering drawings, enforcing ISO standards, and serving as a liaison between quality and operations departments. This opportunity appeals to candidates seeking a role within a fast-growing company that combines the resources of a large public entity with an entrepreneurial culture. The position offers a hybrid work environment with significant desk-based reporting duties and the chance to contribute to innovative data center and utility systems.

This senior engineering role within Vestas Technology focuses on grid compliance and interconnection strategies for renewable energy projects. Based in Houston, the position involves performing advanced power system modeling using tools like PSCAD and PSS/E, conducting interconnection studies for major grid operators, and ensuring compliance with complex grid codes. The engineer will collaborate with global R&D teams and external stakeholders to support wind, solar, and battery storage integration. The role appeals to professionals seeking to lead technical initiatives in the world's largest wind turbine manufacturer, offering a mission-driven environment focused on sustainability. It provides opportunities for professional growth, mentorship of junior staff, and relocation support, with travel required up to 20%.

The Quality Supervisor role supports manufacturing operations by ensuring product quality standards are met through inspection, testing, and documentation. Key responsibilities include performing in-process and final inspections, documenting non-conformances, and leading root cause analysis using Operational Excellence tools like 5S and PDCA. The position also involves auditing Standard Work procedures, training operators, and collaborating with cross-functional teams to drive continuous improvement. This entry-level opportunity appeals to candidates seeking professional growth within a culture that values safety, efficiency, and structured problem-solving. The role offers a supportive environment with opportunities for development, competitive wages, and comprehensive benefits including health insurance and retirement savings.

The Senior Quality Engineer role at Belmar Pharma Solutions ensures products and processes comply with USP, FDA, ISO, and cGMP standards within a leading compounding pharmacy. Key responsibilities include reviewing and approving deviations, investigations, CAPAs, and change controls, while also overseeing validation activities and providing leadership to junior quality engineers. The position offers a collaborative environment focused on wellness and accountability, with opportunities for professional growth through coaching and strategic quality system management. The role is based on-site and requires interaction with cross-functional teams to maintain high clinical support and operational excellence.

The Quality Engineer II role at Nordson EFD supports a global team dedicated to engineered fluid dispensing solutions within a dynamic manufacturing environment. Key responsibilities include leading root cause analysis and corrective actions for customer issues, conducting ISO 9001 audits, and utilizing Lean Six Sigma tools to drive continuous improvement in design and production processes. The position also involves developing quality metrics, training staff on problem-solving methodologies, and supporting new product development with reliability and control plans. This opportunity appeals to candidates seeking a supportive culture that values diversity and invests in professional growth. The role offers a mixed work arrangement across office, lab, and manufacturing settings with minimal travel, providing a platform to advance skills in a growing organization.

This Principal Mechanical Engineer role serves as a technical lead within TransMedics' sustaining engineering team, driving innovation across the company's on-market product portfolio. Key responsibilities include leading end-to-end mechanical design development, conducting advanced structural and thermal analyses, and chairing program-level design reviews. The position also involves defining test methodologies, managing engineering change orders, and collaborating with manufacturing partners to ensure design for manufacturability. The role appeals to candidates seeking to impact patient lives by expanding access to viable donor organs in a mission-driven environment. While the position is based in the Boston area with potential relocation to Somerville by 2028, it offers opportunities for professional growth, cross-functional collaboration, and the chance to shape engineering standards in a high-impact medical technology setting.

This Material Handler role is based at a premier manufacturing facility in Grantsville, Utah, supporting daily operations within a safety-focused environment. Key responsibilities include receiving and inspecting incoming materials, utilizing RF scanners and SAP to manage inventory, and operating material handling equipment to support production lines. The position offers clear pathways for professional growth and training within a reputable industry leader. The role appeals to candidates seeking a supportive culture with competitive pay, weekly pay options, and access to comprehensive benefits including retirement plans and paid holidays. The work arrangement is on-site at the manufacturing facility.

This Principal Product Security Engineer role supports the newly formed Product Security team within Johnson & Johnson's medical device division, focusing on integrating security by design into the product lifecycle. The position requires collaboration with engineering groups to establish and refine security processes, serve as a subject matter expert on cyber risks, and manage pre-market and post-market compliance activities including threat modeling and vulnerability management. The role appeals to candidates seeking to directly impact patient safety while working in a collaborative, patient-first culture. The position is based in Danvers, Massachusetts or Raritan, New Jersey, with a hybrid work arrangement requiring office presence at least three days per week.

The Estimator role at Precise Aerospace Manufacturing supports the engineering and production teams in Yorba Linda by preparing accurate cost estimates and quotations for aerospace and defense projects. Key responsibilities include analyzing engineering drawings and specifications to determine labor and material costs, developing pricing models, and collaborating with purchasing and sales departments to validate timelines and supplier quotes. The position appeals to candidates seeking a stable environment within a premier, ISO-certified company with a history of serving major clients like NASA. The role offers opportunities to contribute to continuous improvement initiatives and cost reduction efforts while working in a collaborative, results-driven culture.

This full-time CNC Programmer role at B & R Machine, Inc. supports high-precision manufacturing for aerospace, defense, and medical sectors within an on-site facility in Ludlow, MA. The position involves creating and optimizing CNC programs using Mastercam and SolidWorks CAM while collaborating with engineering teams to ensure parts meet strict AS9100 and ISO 9001 quality standards. Key responsibilities include interpreting complex engineering drawings, troubleshooting programming issues, and driving continuous improvement initiatives to maximize machine utilization. The role appeals to mid-level professionals seeking a collaborative environment with a diverse fleet of advanced machinery and the opportunity to influence production efficiency in a growing, established company.

This full-time Senior Quality Engineer role supports a high-reliability engineering team focused on optical, mechanical, and electrical products for national security missions. The position involves developing quality assurance plans, ensuring compliance with industry standards like AS9100, and leading root cause analysis for manufacturing anomalies. Key duties include auditing fabrication processes, managing supplier qualifications, and chairing Material Review Boards to resolve non-conformances. The role offers a culture of integrity with a focus on continuous growth, providing autonomy through flexible time off and access to robust learning resources. While the position requires U.S. citizenship and the ability to obtain a security clearance, it supports a mission-driven environment dedicated to advancing critical national objectives.

The Program Manager II role leads cross-functional teams within Forj Medical to deliver complex medical device projects on time and within budget. Key responsibilities include managing customer expectations, negotiating contract changes, and coordinating schedules, budgets, and scope across engineering, manufacturing, and supply chain departments. The position requires guiding multiple medium-scale programs while ensuring compliance with FDA and ISO regulations. This opportunity appeals to professionals seeking a dynamic environment where they can drive process improvements and add value to diverse customer products. The role operates in a matrixed organization with a focus on collaboration and independent leadership.

This Principal Product Security Engineer role supports the newly formed Product Security team within Johnson & Johnson's medical device division. The position focuses on embedding security by design throughout the product lifecycle, from pre-market development to post-market vulnerability management. Key responsibilities include partnering with engineering teams to enforce security policies, creating and improving security processes, and generating critical documentation such as threat models and risk management plans. The role also involves guiding compliance certification activities and advising on balancing business needs with medical device security objectives. This opportunity appeals to candidates seeking to directly impact patient lives within a Patient First culture. The position is based in Danvers, MA or Raritan, NJ, with a hybrid work arrangement requiring office presence at least three days per week.

This Principal Product Security Engineer role supports the newly formed Product Security team within Johnson & Johnson's medical device division. The position focuses on embedding security by design throughout the product lifecycle, from pre-market development to post-market vulnerability management. Key responsibilities include partnering with engineering teams to enforce security policies, creating and improving security processes, and delivering critical documentation such as threat models and risk management plans for regulatory compliance. The role appeals to candidates seeking to directly impact patient lives by shaping industry standards in a collaborative, patient-first culture. While the position is primarily based in Danvers, MA or Raritan, NJ with a requirement to be in-office at least three days per week, remote work options may be considered on a case-by-case basis.

This Principal Product Security Engineer role supports the newly formed Product Security team within Johnson & Johnson's medical device division. The position focuses on embedding security by design throughout the product lifecycle, from pre-market development to post-market vulnerability management. Key responsibilities include partnering with engineering teams to enforce security policies, creating and improving security processes, and delivering critical documentation such as threat models and risk management plans. The role also involves guiding compliance certification activities and advising development teams on balancing business needs with medical device security objectives. This opportunity appeals to candidates seeking to directly impact patient lives within a collaborative, patient-first culture. The position is based in Danvers, MA or Raritan, NJ, with a hybrid work arrangement requiring office presence at least three days per week.

This Principal Product Security Engineer role supports the newly formed Product Security team within Johnson & Johnson's medical device division. The position focuses on embedding security by design throughout the product lifecycle, from pre-market development to post-market vulnerability management. Key responsibilities include partnering with engineering teams to enforce security policies, creating and improving security processes, and delivering critical documentation such as threat models and risk management plans. The role appeals to candidates seeking to directly impact patient lives by shaping industry standards and ensuring compliance with rigorous regulatory frameworks like FDA, ISO 27001, and SOC2. The position is based in Danvers, MA, or Raritan, NJ, with a hybrid work arrangement requiring office presence three days per week, offering a collaborative environment within a Patient First culture.

This Principal Product Security Engineer role supports the newly formed Product Security team within Johnson & Johnson's medical device division, focusing on integrating security by design into the product lifecycle. The position requires partnering with engineering groups to enforce security policies, develop risk management documentation, and guide teams through pre-market and post-market compliance activities. Key responsibilities include creating security processes, acting as a subject matter expert on cyber threats, and supporting certifications such as SOC2 and ISO 27001. The role is based in Danvers, MA, with a hybrid schedule requiring three days in the office, though remote options may be considered. The position appeals to candidates seeking to impact patient safety directly within a collaborative, patient-first culture while shaping industry standards for medical device security.

This Principal Product Security Engineer role is part of the Technology Enterprise Strategy & Security team within Johnson & Johnson's medical device division. The position focuses on embedding security by design into the product development lifecycle, partnering with engineering groups to ensure adherence to security policies and regulatory standards. Key responsibilities include creating and improving security processes, acting as a subject matter expert on cyber security matters, and delivering critical documentation for pre-market activities and compliance certifications such as SOC2 and ISO 27001. The role appeals to candidates seeking to directly impact patient lives through innovative security solutions in a regulated environment. The position is based in Danvers, MA, with a hybrid work arrangement requiring office presence three days per week, though remote options may be considered on a case-by-case basis.