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About TE Connectivity

TE Connectivity is a $13 billion global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions, proven in the harshest environments, enable advancements in transportation, industrial applications, medical technology, energy, data communications, and the home. With nearly 80,000 employees, including more than 8,000 engineers, working alongside customers in approximately 150 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at www.te.com and on LinkedIn, Facebook, WeChat and Twitter.

What TE Connectivity offers:

We offer competitive total rewards compensation. Our commitment to our associates includes offering benefit programs that are comprehensive, competitive and will meet the needs of our associates.

  • Generous 401(k) Plan
  • Tuition Reimbursement
  • Benefits start on day one
  • Charity Donation Matching Program
  • Competitive Paid Time Off
  • Employee Resource Groups
  • Employee Stock Purchase Program
  • Healthcare for Associates and Families
  • Health and Wellness Incentives
  • Life Insurance and Disability Protection

Throughout our Global reach and various Business Units, we take a balanced approach to the benefits we provide. Many benefits are company-paid, while others are available through associate contribution. Specific benefit offerings can vary by location.

Job Overview

TE Connectivity’s Quality and Reliability Engineering Teams analyze the ability of product and production systems to comply with customer and contractual requirements through established reliability factors. They design, recommend revisions and install quality control systems, develop and document analytical methods for establishing reliability of products and their components and conduct analysis on relative reliability with regards to cost, structure, weight, maintainability, facility of production, and availability of materials and equipment. Out teams develop, implement and monitor company environmental safety programs and policies to ensure compliance with federal, state, and local environmental, health and safety regulations and recommend corrective actions if necessary. They are responsible for policies and practices to comply with applicable government regulations and industry requirements related to product environmental compliance, the implementation and management of technical and testing standards and specifications, quality control and reliability programs governing materials, product and processes, resulting in the optimization of material and labor, as well as failure analysis, root cause, corrective action and customer communication.

Responsibilities & Qualifications

•    Maintain and comply with the requirements of ISO13485, GMP/GDP (Good Manufacturing Practices/Good Documentation Practices), US FDA 21 CFR Part 820, MDSAP (QMS Regulation for US and Canada), European MDD/MDR (Medical Device Directive/Medical Device Regulation),  and other applicable regulations. 
•    Implementation of quality system documentation that is in compliance with the quality manual and associated Standard Operating Procedures (SOPs). 
•    Support in developing and execution of Validation Master Plans, Equipment Qualifications, Process Validations, and test method validations for successful transfer from development to manufacturing working in a cross-functional group. 
•    Ensure that required specifications are implemented for incoming/ in-process/ outgoing quality inspections. 
•    Support in developing and maintaining the dFMEA/pFMEA process for finished good medical devices working in a cross-functional group. Support/participate in regulatory agency and customer quality audits. 
•    Participate in design control activities to ensure that product meet specifications, reliability, and manufacturability. 
•    Working knowledge of CAPA management to drive to root cause analysis and practical corrective and preventive solutions. Utilize formal problem-solving techniques to resolve product and/or process related issues.
•    Write and or assist in development of protocols, technical investigation plans, engineering reports, and related procedures which ensure statistical validity, adequacy, and compliance to regulatory and corporate requirements. 
•    Working knowledge of concepts of probability and statistics as well as aide in updating/ establishing SPC and Gage R&R studies. 
•    Work with suppliers of both raw materials and components to improve product quality and/or resolve quality issues. 
•    Establishing inspection standards, plans, frequencies and test methods. 
•    Support Production on all quality-related activities, including working closely with Engineering and other applicable functions.

What your background should look like:

•    BS/BA degree with a scientific/engineering emphasis required. 
•    Senior Quality Engineer Experience 
•    Minimum of 3 years' experience in a regulated medical device environment (contract manufacturing or OEM) 
•    Excellent communication and interpersonal skills, proven problem-solving capability 
•    Six Sigma Green/Black belt preferred 
•    ASQ Certified Quality Engineer or MS degree desirable 
•    Catheter experiences desirable


•    Values: Integrity, Accountability, Teamwork, Innovation 
•    Written Communications Vision and Values 
•    Understanding Others Total Work Systems (e.g., TQM/ISO/Six Sigma) 
•    Timely Decision Making 
•    Time Management 
•    Technical Skills 
•    Team Leadership 
•    Quality 
•    Problem Solving/Analysis 
•    Planning

•    Values: Integrity, Accountability, Teamwork, Innovation 
•    Written Communications Vision and Values 
•    Understanding Others Total Work Systems (e.g., TQM/ISO/Six Sigma) 
•    Timely Decision Making 
•    Time Management 
•    Technical Skills 
•    Team Leadership 
•    Quality 
•    Problem Solving/Analysis 
•    Planning

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. 


Hermosillo, SON, MX, 83200

City:  Hermosillo
State:  SON
Country/Region:  MX
Travel:  More than 75%
Requisition ID:  80804
Alternative Locations: 
Function:  Engineering & Technology

Job Segment: Manufacturing Engineer, Engineer, Developer, CAPA, Web Design, Engineering, Technology, Management, Creative

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