TE Connectivity
QLTY & RELIABILITY ENGINEER II
Ensures that products being built and processes being used adhere to all standards and requirements; implements quality assurance practices, processes, and procedures. Reporting to the Quality Manager/Quality Supervisor, the Quality Engineer is a member of the Quality group. The successful candidate will be responsible for Quality within their prescribed area of functional responsibility. They will be working as part of a team to maintain high quality/performance standards on all TE Connectivity products. This challenging position will require an ability to work within a collaborative environment, pursuing continuous improvement and ensuring compliance to the TE Connectivity Quality System. The focus of the role is to supply high-quality medical devices and components to deliver an Extraordinary Customer Experience. Job Requirements
Working cross functionally with other departments promote the achievement of the health and safety goals. To deliver on all KPIs that help the business achieve its goal. The Quality Engineer will perform an active role in further development and continuous improvement of the Quality Management system. Establish and maintain risk management principles and methods throughout the product realization process in compliance with the company's Quality Management system and applicable regulations. Maintain relevant documentation to comply with quality standards and customer requirements. Offer quality guidance to the entire team in support of the day-to-day deliverables. Develop strong links with customer organizations and other project stakeholders. Support and initiate projects to ensure continuous improvement. Quality review of responsible area validation documentation. Investigation of root cause and implementation of effective corrective actions to prevent re-occurrence of compliance issues. Overall responsibility for production GMP standards and compliance. Establish inspection standards, sampling plans and test methods where applicable. Prepare and update procedures and associated documentation. Support customer audits and surveillance/accreditation audits. Conduct and drive audits ensuring compliance with ISO13485. The Quality Engineer will perform an active role in quality planning and new product introduction from a quality perspective. Develop strong links with customer organizations and other project stakeholders. Quality review of responsible area validation documentation. What Your Background Should Look Like
Bachelor's degree in Quality or Degree in Science / Engineering / Quality field. Minimum of 3 years of progressively responsible professional level industry experience is required. Key Requirements Working knowledge of FDA/ISO/MDD Quality systems for Medical Device companies. Experience within a similar role as Quality Engineer is an advantage. Quality experience in component and device manufacturing desirable. Excellent written and oral communication skills essential. Competencies
Values: Integrity, Accountability, Inclusion, Innovation, Teamwork
Ensures that products being built and processes being used adhere to all standards and requirements; implements quality assurance practices, processes, and procedures. Reporting to the Quality Manager/Quality Supervisor, the Quality Engineer is a member of the Quality group. The successful candidate will be responsible for Quality within their prescribed area of functional responsibility. They will be working as part of a team to maintain high quality/performance standards on all TE Connectivity products. This challenging position will require an ability to work within a collaborative environment, pursuing continuous improvement and ensuring compliance to the TE Connectivity Quality System. The focus of the role is to supply high-quality medical devices and components to deliver an Extraordinary Customer Experience. Job Requirements
Working cross functionally with other departments promote the achievement of the health and safety goals. To deliver on all KPIs that help the business achieve its goal. The Quality Engineer will perform an active role in further development and continuous improvement of the Quality Management system. Establish and maintain risk management principles and methods throughout the product realization process in compliance with the company's Quality Management system and applicable regulations. Maintain relevant documentation to comply with quality standards and customer requirements. Offer quality guidance to the entire team in support of the day-to-day deliverables. Develop strong links with customer organizations and other project stakeholders. Support and initiate projects to ensure continuous improvement. Quality review of responsible area validation documentation. Investigation of root cause and implementation of effective corrective actions to prevent re-occurrence of compliance issues. Overall responsibility for production GMP standards and compliance. Establish inspection standards, sampling plans and test methods where applicable. Prepare and update procedures and associated documentation. Support customer audits and surveillance/accreditation audits. Conduct and drive audits ensuring compliance with ISO13485. The Quality Engineer will perform an active role in quality planning and new product introduction from a quality perspective. Develop strong links with customer organizations and other project stakeholders. Quality review of responsible area validation documentation. What Your Background Should Look Like
Bachelor's degree in Quality or Degree in Science / Engineering / Quality field. Minimum of 3 years of progressively responsible professional level industry experience is required. Key Requirements Working knowledge of FDA/ISO/MDD Quality systems for Medical Device companies. Experience within a similar role as Quality Engineer is an advantage. Quality experience in component and device manufacturing desirable. Excellent written and oral communication skills essential. Competencies
Values: Integrity, Accountability, Inclusion, Innovation, Teamwork