April 30, 2026For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at LeidosCareersFraud@leidos.com.
May 29, 2026For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at LeidosCareersFraud@leidos.com.
Job Description: FM Approvals is an international leader in third-party testing and certification services.
Qualifications:
- MS or BS in Engineering, Electrical or Electro-Mechanical highly preferred + 2+ years of related experience.
p/>FM Approvals is seeking a highly motivated business development advanced engineer to support growth in the Hazardous Location, and Industrial Internet of Things (IioT) markets.
Qualifications:
You will work directly with suppliers to resolve issues, drive corrective actions, and communicate requirements, while also performing supplier audits and contributing to larger, moderately complex projects. Collaborate across engineering, supply chain, and operations to ensure quality issues are resolved and supplier capabilities are aligned with program needs.
For more than 70 years, Senior Metal Bellows has been pushing the limits of innovation-designing and building custom-engineered metal bellows for industries that demand the best: aerospace, defense, energy, and beyond. This position is posted as a multi-level role (Quality Engineer or Senior Quality Engineer) to match candidates with the appropriate level based on experience, technical capability, and demonstrated impact.
strong> Job Description:- We are looking for an experienced Supplier Quality Engineer with 6 8 years of experience in supply chain, operations, engineering, or quality management within regulated industries such as Medical Devices, Pharmaceuticals, or Life Sciences. Strong knowledge of supply chain processes, sourcing, demand and supply planning, ERP/PLM systems, and change management is required.
p>For more than 70 years, Senior Metal Bellows has been pushing the limits of innovation-designing and building custom-engineered metal bellows for industries that demand the best: aerospace, defense, energy, and beyond. Act as the key liaison between internal engineering/operations teams and external manufacturing partners to drive alignment on changes, escalations, and quality expectations.
New Bedford, MA30+ days ago
Partnering cross-functionally with Manufacturing, R&D, Supply Chain, and external suppliers, the Senior Engineer provides technical expertise in root cause analysis, corrective and preventive actions, and new product introductions. The Senior Engineer, Central Quality & Quality Control plays a critical role in driving excellence across manufacturing operations and supplier networks by ensuring consistent product performance and compliance with Acushnet Company Quality System requirements.
Details of ZOLL's comprehensive benefits plans can be found at www.zollbenefits.com. The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally.
strong> Job Description:- We are looking for an experienced Supplier Quality Engineer with 6 8 years of experience in supply chain, operations, engineering, or quality management within regulated industries such as Medical Devices, Pharmaceuticals, or Life Sciences. Strong knowledge of supply chain processes, sourcing, demand and supply planning, ERP/PLM systems, and change management is required.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market.
New Bedford, Massachusetts30+ days ago
Please click here for more details. The Senior Engineer, Central Quality & Quality Control plays a critical role in driving excellence across manufacturing operations and supplier networks by ensuring consistent product performance and compliance with Acushnet Company Quality System requirements.
New Bedford, MA30+ days ago
Placement in the range depends on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, relevant experience, skills, seniority, performance, shift, travel requirements, and business or organizational needs and may change over time. Reporting to the Quality Director, this person will be responsible for identifying opportunities for continuous improvement, formulating corrective and preventive actions, and working to implement those actions to improve quality levels and regulatory compliance.
USA Wilmington, Massachusetts22 days ago
Encompassing product, site, manufacturing, and supplier Quality, the team focuses on quality planning, defect prevention, and process validation from prototype through production, using product and field data to drive continuous improvement. Applying next-gen technology, high-density storage and machine learning to solve today's complex distribution challenges, Symbotic enables companies to move goods with unmatched speed, agility, accuracy and efficiency.
This position is tasked with leading supplier improvement and supplier development activities to ensure suppliers have excellent measurement system capability, process capability, and process controls. The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally.
New Bedford, Massachusetts22 days ago
Our model to serve our customers where they need us has led to a diversified product range using our unparalleled expertise in ceramic and carbon materials, which we exploit to solve difficult problems for our customers across a diverse range of markets. That means leading complex investigations, running CAPAs that actually stick, working directly with customers and auditors, and keeping the Quality Management System doing what it’s meant to do — not just looking good on paper.
p>Required Skills: • Self-motivated and detail-driven professional with a passion for quality and compliance • Experienced in manufacturing, quality control, and audit practices • Comfortable working independently and managing your own schedule • Tenured audit experience with demonstrated proficiency performing conformity assessment audits • Ability to obtain and assess objective evidence throughout the audit process while acting impartially and maintaining confidentiality • Observe, document, and evaluate audit observations while effectively managing customer interactions throughout the audit process • Possess critical thinking, analytical and problem-solving skills • Computer literacy with demonstrated proficiency in Microsoft Office Suite • Experience with various measurement tools such as pressure gauges, calipers, voltmeters, etc. Key Responsibilities: • Conduct on-site audits of manufacturing facilities to verify compliance with FM Approvals requirements • Review technical documentation, product markings, inspection equipment, and calibration records for compliance • Deliver clear, professional audit reports and communicate findings with all stakeholders • Build strong relationships with manufacturers by managing customer interactions and maintaining integrity, impartiality and confidentiality throughout the audit process • Document facts and observations to support audit findings and conclusions • Efficiently manage audit schedules.
li>Partner with development engineering, product quality engineering, Product sourcing engineering, Global Strategic Sourcing and program management to deliver predictable supply to the development programs, production programs, and manage exceptions/containments/deviations for supplier technical performance, particularly in the development phases. Review supplier processes and capabilities to ensure alignment to electrical performance & sub-assembly requirements can be achieved, including driving supplier QC processes (i.e. cell compliance before assembly, welded cell block validation, and complete module/pack end-of-line outgoing quality processes match incoming quality checks).
p>This is a high-impact role responsible for stabilizing and strengthening the Quality Management System (QMS), supporting production output, managing facility transfer activities, and ensuring compliance with FDA and ISO 13485 requirements within a medical device manufacturing environment. Supports Change Control, works with the Cross-Functional Team for Impact Assessment, and ensures the timely completion of activities while updating relevant documents.
p>We're looking for people who like solving hard, practical problems and want to have a direct impact on how JaiaBot Systems gets built, tested, and deployed. If you enjoy taking low rate initial production hardware and turning it into a defined, scalable process or mass production, this role is for you.
ul>Collaborate with IT and system business owners to ensure internal CSV processes and procedures are aligned to GAMP 5, 21 CFR Part 11, EU Annex 11, ICH Q9 (risk management), ICH Q10 (PQS), and FDA's Computer Software Assurance (CSA) guidance. Primary skills and knowledge required include, but are not limited to the following:
- Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
Us, Massachusetts6 days ago
Learn more at www.analog.com and on LinkedIn and X. For positions requiring access to technical data, Analog Devices, Inc. may have to obtain export licensing approval from the U.S. Department of Commerce - Bureau of Industry and Security and/or the U.S. Department of State - Directorate of Defense Trade Controls.
West Warwick, RI30+ days ago
Product brands within the Worthington Enterprises portfolio include Balloon Time, Bernzomatic, Coleman (propane cylinders), CoMet, Elgen, Garden Weasel, General, HALO, Hawkeye, Level5 Tools, Mag Torch, NEXI, Pactool International, PowerCore, Ragasco, Well-X-Trol and XLite, among others. Key position results include but are not limited to, increase quality at and/or reduced cost for supply base, internally and customer base; compliance with all regulatory and internal policies; reduction in scrap, reject and rework; and timely and accurate CAR preparation and evaluation.
Providence, RI11 days ago
p>Job Description: We are looking for a Quality Engineer that will be responsible for providing hands-on manufacturing quality support across production, receiving inspection, testing, supplier quality activities, and program execution. This role ensures product compliance, configuration control, effective corrective actions, and adherence to customer, regulatory, and company quality requirements while supporting production objectives and customer deliverables.
Additionally, you will participate in New Product Introduction and First Time Build review, develop Quality Control Plans, and implement strategies aimed at achieving zero defects in the production process. As a Quality Engineer, you will lead and manage Corrective and Preventive Actions (CAPA) to resolve quality issues using the 8D process for evaluating and documenting non-conforming products and processes.
Mansfield, MA30+ days ago
p>Subject to the terms of their respective policies and date of hire, Employees are eligible for the following https://jobs.integralife.com/total-rewards/. • Bachelors degree or equivalent with 8+ years of experience, Master degree with 5+ years of experience, Doctoral degree with 3+ years of experience • This position will require relevant experience working in manufacturing/operations.
The company's American-made products, which include lighting, print graphics, digital graphics, refrigerated and custom displays, aim to help businesses stand out in a competitive market. EMI Acquisition Company Inc. (dba: EMI Industries) creates custom fixtures, displays and food equipment for the nation's premier grocery, retail and restaurant brands.
li>Must possess a well-rounded background in Semiconductor/Electronics manufacturing, with particular focus on product life cycle, trouble-shooting and inspection of manufacturing processes. Individual salaries are determined based upon a variety of factors including but not limited to, a candidates overall qualifications, such as skills, education, and experience as well as company internal equity.
West Warwick, RI30+ days ago
Audits and Compliance: Lead internal audits, customer audits, and third-party audits; prepare documentation, support on-site activities, and ensure timely closure of audit findings. This role has no direct reports and works cross-functionally with Operations, Engineering, R&D, and Customer Service to ensure compliance with customer, regulatory (ISO, FDA, Organic, etc.), and internal requirements.
These include but are not limited to computer training, reviewing and updating work instructions, problem solving and communication techniques \nSuggests, collaborates and implements/improves on effective work methods, machinery, documentation, materials, safety and team projects that could improve safety, products, profits, cost or scrap. \nSkilled at attacking problems and projects with drive and energy with an eye on quality, cost, and customer service.\n \nEssential Experience and Qualifications\n \nBachelor's Degree in the Engineering, Electronic, Electro-mechanical or Mechanical disciplines, or equivalent.
Franklin Town, MA30+ days ago
p>iAutomation, a full-service automation company, developing robotic solutions and offering design, engineering, and integration (DE&I) services, product support, and production services, has an immediate opening for a Quality Engineer in Franklin, Massachusetts. The Quality Engineer is the Quality point of contact for iAutomation’s top and strategic customers, for customer driven actions & requests, and Quality Engineering support.
What you'll be doing as a Quality Engineer: Assist quality engineering with generation of testing and qualification test instructions, finding sources for testing and testing equipment, performing internal testing, maintaining test and quality records and samples, observe external testing as required. Knowledge and skills: quality systems and project management experience, procedure documentation, detail oriented and organized, strong communication skills, customer service experience, interpersonal skills, excellent verbal and written communication skills, effective team player, and critical thinking skills.
Working knowledge of product development methodologies such as Failure Modes and Effects Analysis (FMEA), Advanced Product Quality Planning (APQP), Production Part Approval Process (PPAP) elements such as Measurement Systems Analysis (MSA), and Geometric Dimensioning and Tolerancing (GD&T). Partner with the manufacturing engineering, production, and development engineers to support the quality of the integration process for components such as underwater sensors/equipment, PCBAs, cables, wiring harness, actuators, machined parts and structures, etc.
p style="margin:0in">If you have the courage to take on a wide variety of complex challenges, then you will experience a unique working environment where innovative teams blend different perspectives, disciplines, and technologies to discover new ways of solving complex problems. Company Overview: We are a world-class team of professionals who deliver next generation technology and products in robotic and autonomous platforms, ground, soldier, and maritime systems in 50+ locations world-wide.
p>Responsibilities: - Provide expertise and general oversight for the management and improvement of Nova Biomedicals Quality Systems, including quality planning, quality control planning, internal auditing, inspection procedures, document controls, change management, process controls, quality records, corrective and preventive activities, validations, and data management. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences.
li>Prepare for and support internal and external audits by ensuring audit readiness, compiling objective evidence, coordinating with process owners, supporting auditor interviews, and assisting with timely corrective action responses in alignment with MDSAP requirements. S.) in Life Sciences or Engineering, or equivalent experience with an in-depth working knowledge of quality systems for medical devices, preferably in orthopedics, including but not limited to: 21 CFR 820, 21 CFR 11, EN ISO 13485, Directive 93/42/EEC.
Sensata Technologies is a leading industrial technology company that develops sensors, sensor-based solutions, including controllers and software, and other mission-critical products to create valuable business insights for customers and end users. Handles design methods and procedures for inspecting, testing, and evaluating the precision and accuracy of production processes, production equipment and finished products.
Providence, RI30+ days ago
As the world's only end-to-end professional services firm focused on MedTech, we take clients' Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting. Provides input and/or oversight for quality system related activities, including complaint handling, CAPA investigation and supplier evaluations, as needed to assist clients in ensuring product quality and proper implementation of compliant processes.
Ultra Maritime considers multiple factors when determining final compensation, including the scope and responsibilities of the role, a candidate's relevant experience and education, certifications and training, as well as current business and market conditions. Due to the nature of the programs we support, certain roles may require candidates to meet U.S. nationality requirements and be eligible to obtain a security clearance.
We deliver industry-changing innovations and next-generation solutions for extrusions; diagnostic and interventional catheters; balloons and balloon catheters; sheath/dilator sets; specialty sutures, braids and fibers; and bioabsorbable sutures, yarns and resins. We set ourselves apart with deep expertise, decades of experience, a dedication to design for manufacturability, and extensive, in-house capabilities, which include engineering, regulatory services, material selection and formulation, prototyping, manufacturing, assembly and packaging.
The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare.
- The Senior Design Quality Engineer will support product lifecycle management activities for medical devices by providing quality engineering leadership for design and process changes, risk management, verification and validation activities, and compliance with medical device regulations.
- The role requires close collaboration with cross-functional teams including R&D, Manufacturing, Regulatory Affairs, Marketing, and Operations.
With Diversity, Equity, and Inclusion (DE&I) as part of our Social Ambition 2030 and a strategic pillar of our Company culture, Prysmian is committed to the development of an organization that prioritizes talent, where people feel respected, included, and free to fully express their potential just as they are. Each year Prysmian manufacturers thousands of miles of underground and submarine cables and systems for power transmission and distribution, as well as medium low voltage cables for the construction and infrastructure sectors.
ul>Inclusion and Belonging- Committed to Welcoming, Celebrating and Thriving on Inclusion and Belonging, Learn more about Employee Inclusion Groups on our website (https://www.smith-nephew.com/en/careers). The actual base pay offered to the successful candidate will be based on multiple factors, including but not limited to job-related knowledge/skills, experience, geographical location, and internal equity.