Defect Prevention Engineer

**Job Title**: First Time Quality Engineer**First Time Quality Engineer****Role overview**This role will support the implementation of the First Time Quality (FTQ) program across various operations sites within Philips.The FTQ program aims to foster a culture of defect prevention by proactively identifying and mitigating risks at the source, thereby ensuring...

About the RoleThe First Time Quality (FTQ) program at Philips is a key initiative aimed at fostering a culture of defect prevention. As an FTQ Engineer, you will play a pivotal role in driving this initiative forward.ResponsibilitiesSupport the execution of FTQ events at operations sites, focusing on identifying conditions required for producing good parts...

Job OverviewThis role will support the implementation of the FTQ program across various operations sites within Philips. The FTQ program aims to foster a culture of defect prevention by proactively identifying and mitigating risks at the source.Key ResponsibilitiesExecute FTQ events at operations sites to identify conditions required for producing good parts...

Johnson & Johnson is a global healthcare leader that aims to change the trajectory of health for humanity. Our Innovative Medicine and MedTech solutions empower us to deliver breakthroughs in prevention, treatment, and cure of complex diseases. As a Cloud Engineer at Johnson & Johnson, you will play a crucial role in shaping our cloud infrastructure on...

Our Department in Athens is looking for a motivated software back-end engineer to work with client/s in the European Public sector such as European Commission European Patent Office, European Medicines Agency, United Nations and NATO.You will be part of a multicultural, high-performing, cross-functional and agile team responsible for the design,...

Manufacturing Engineering for Transfer support.- Elaborate validation and transfer strategies in collaboration with MDT counterparts.- Review and approve TMV/QBE plan and reports.- Create engineering rationales in collaboration with MDT counterparts.- Draft, submit and follow up Validation Master Plans and Reports for approval process.- Draft, submit and...

High School diploma.- 2+ year(s) of working experience in corporate customer service, back-office or contact center corporate environments.- B2 English proficiency.This is a non-virtual, full-time, permanent, exempt (non-hourly) position based in Costa Rica and does not offer relocation benefits.Job applicants must be located and legally authorized to work...

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.Job Overview This position will provide environmental, health and safety support to manufacturing and administrative areas, through improvement and implementation of health and safety culture, incident...

Job DescriptionResponsible for analyzing, designing, developing, maintaining, evaluating and assuring the quality and performance of different software system components and their respective relationships, supporting and guiding others in his work team.Key roles, Responsibilities and Functions:Define the quality control process for the project and its...

**Careers that Change Lives**We're a mission-driven leader in medical technology and solutions with a legacy of integrity and innovation.Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 90,000+ passionate people.Powered by our diverse knowledge, insatiable curiosity, and desire to help all those who need it, we...

Education / Educación:- Bachelor's degree in Engineering or related fieldSpecialized Knowledge / Conocimiento especializado:- Knowledge of FDA Medical Device Regulations including Quality System Regulation 21 CFR Part 820- ISO 13485:2003- Canadian MDR, and Medical Device DirectiveLanguages required for the position / Idiomas requeridos para el puesto:-...

Manufacturing Engineering for Transfer support. - Elaborate validation and transfer strategies in collaboration with MDT counterparts. - Review and approve TMV/QBE plan and reports. - Create engineering rationales in collaboration with MDT counterparts. - Draft, submit and follow up Validation Master Plans and Reports for approval process. - Draft, submit...

Education / Educación: - Bachillerato Universitario en ingeniería o carrera a fin. Specialized Knowledge / Conocimiento especializado: - Estadística, manejo de proyectos, preferiblemente CQE Languages required for the position / Idiomas requeridos para el puesto: - Español / Inglés Avanzado Computer tools and knowledge level required /...

Education / Educación: - Bachillerato Universitario en ingeniería o carrera a fin. Specialized Knowledge / Conocimiento especializado: - Estadística, manejo de proyectos, preferiblemente CQE Languages required for the position / Idiomas requeridos para el puesto: - Español / Inglés Avanzado Computer tools and knowledge level required /...

Education / Educación: - Bachelor's degree in Engineering or related field Specialized Knowledge / Conocimiento especializado: - Knowledge of FDA Medical Device Regulations including Quality System Regulation 21 CFR Part 820 - ISO 13485:2003 - Canadian MDR, and Medical Device Directive Languages required for the position / Idiomas requeridos para el...