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Job Overview
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 and will work 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 with 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.
Responsibilities
Working cross‑functionally with other departments to promote the achievement of health and safety goals
Deliver on all KPIs that help the business achieve its goal
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 day‑to‑day deliverables
Develop strong links with customer organizations and other project stakeholders
Support and initiate projects to ensure continuous improvement
Review responsible area validation documentation
Investigate root cause and implement 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
Perform an active role in quality planning and new product introduction from a quality perspective
Qualifications
Level 8 degree in Quality or Degree in Science / Engineering / Quality field
Minimum of 2 years of industry experience is required
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
Benefits
Competitive Salary Package
Performance‑Based Bonus Plans
Health and Wellness Incentives
Employee Stock Purchase Program
Community Outreach Programs / Charity Events
Employee Resource Group
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