Applicants must be legally authorized to work in the United States. We are unable to sponsor or take over sponsorship of a school/employment or any other visa , regardless of expiration date, now or in the
This role is responsible for the generation, implementation, and management of a Manufacturing focused Meta Quality Program, by establishing a Quality Program that is focused on people, processes and accountability through influential vendor management and effective partnerships with site-based
Date Posted:2026-06-29 Country:Poland Location:PL-POLAND-REMOTE Position Role Type:Remote At Collins Aerospace, we’re working side-by-side with our customers and partners to dream, design and deliver solutions that redefine the future of our industry. We’re reaching across markets, disciplines
Position Summary This position ensures products meet safety, regulatory, and quality standards throughout the product lifecycle, from design and development to post-market surveillance for medical devices within combination products. Responsibilities include risk management, participation in root cause
Company Summary We are a global company of problem solvers, collaborators, and innovators with platforms in HVAC and Detection & Measurement. We build innovative solutions that enable a safer, more efficient, and sustainable world. Job Summary
Job Description: An opportunity for a Airworthiness & Quality Engineer (Logistics/Procurement) has arisen within Airbus Defence and Space, Getafe (Madrid). The selected candidate will join the Quality Logistics and Transport Team (part of Procurement Quality). Our main mission is to
Acute Care TechnologyThis is a 2nd shift opportunity JOB SUMMARY Responsible for partnering with the manufacturing, engineering and quality teams in the design, implementation and validation of new processes to manufacture high quality medical devices and associated accessories. Utilizes
Position Summary Provide quality support for ICU Medical Hardware and development. The Sr. Quality Engineer will be responsible for development procedures and deliverables, ensuring their compliance with ICU Medical quality system requirements and applicable regulations and standards (such as ISO
Our story began with a passionate idea that we could change the world. And to be honest, we’ve never stopped believing that. In 1986 it was a simple concept that microbiology teamed with innovation and clinical
Are you interested in being part of an innovative team that supports Westinghouse’s mission to provide clean energy solutions? At Westinghouse, we recognize that our employees are our most valuable asset and we seek to identify,
Are you interested in being part of an innovative team that supports Westinghouse’s mission to provide clean energy solutions? At Westinghouse, we recognize that our employees are our most valuable asset and we seek to identify,
The Quality Engineer II will utilize and maintain quality engineering systems and practices in collaboration with Agiliti manufacturing and design centers that meet and exceed internal, customer, and regulatory requirements. Location for this role is flexible / can work remote
Dover is a diversified global manufacturer with annual revenue of over $8 billion. We deliver innovative equipment and components, specialty systems, consumable supplies, software and digital solutions, and support services through five operating segments: Engineered Products,
At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world’s most innovative companies unleash their potential. From autonomous cars to life-saving robots, our
Job Description Spectroscopy Product owner coupler with Manufacturing test development. Collaborate with the product design team to determine product testing parameters Design, refresh or sustain tester software to meet product or sub module test parameter requirement. self-initiative
As a Quality and Regulatory Engineer on our Fluke Health Solutions Quality Assurance/Regulatory Affairs team, you will be responsible for maintaining compliance with ISO 17025, NQA‑1, 10CFR 50 Appendix B, ISO 9001 and other applicable regulatory Agencies (NUPIC) &
Job SummarySupport Medline’s Supplier Quality operations by executing supplier qualification, monitoring, and performance activities for a global supply base. This role assists with supplier assessments, documentation review, audits, and issue resolution to ensure compliance with FDA regulations,
Basic Qualifications Bachelors degree in Software Engineering, or related Science, Technology, Engineering or Mathematics field, plus a minimum of 8 years of relevant experience; or Masters degree, plus 6 years relevant experience. Responsibilities for this Position
Test Engineer 4 Position Summary: The Manufacturing Engineer, Silicon Photonics owns day-to-day test engineering support for Silicon Photonics products manufactured at our supplier in Taipei. The role is central to ensuring stable production output, resolving yield and throughput issues,
Global NPI Manufacturing Systems Engineer Location: Poland (Hybrid) Travel: International travel required (approximately 15–25%) About the Role We are seeking an experienced and highly motivated Global NPI Manufacturing Systems Engineer to support New Product Introduction (NPI) activities across our international