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 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. What your background should look like: SHIFT B: from Monday to Friday, 3:30 p.m. to 10:00 p.m and Saturdays from 7:00 a.m. to 2:00 p.m

 

KEY RESPONSIBILITIES& TASKS 

 

Maintain Quality Management System documentation files, verifying formats and revisions. Review changes to product configuration and manufacturing control process documentation. Timely distribution of the most current revision documentation to all users. Remove obsolete documentation at points of use and system. Receive and perform final review of Job Traveler’s process to ensure compliance with good documentation practices. Perform tasks as defined in document control procedures Create and follow up on NCMR's. Safeguard controlled documents including Drawings, Quality Manual, Standard Operating Procedures, work instructions, grinding process forms, Charts, job travelers, material specifications and others. Participate in tasks as assigned by the Quality Manager, related to the Quality Management System. May also support Internal Audits and Management Review processes. Must be able to support departments such as Doc Control, Training, Calibrations, Incoming, Environmental Monitoring, Pest Control and Methods.

SKILLS

Language: Bilingual English (Intermediate)/ Spanish.  Knowledge in Microsoft Office. Excel and Word intermediate mainly. Ability to communicate effectively orally and in writing. Ability to read and interpret changes in documents, such as, job travelers, sketches, diagrams, blueprints and other procedures. Proficient in geometry, fractions, percentages, ratios and measurements. Ability to gather relevant data, establish facts and find solution through actions. Problem solving. Effective time management/organization skills, applied in a pressured environment. Ability to work independently and in a team environment. Effective interpersonal skills and proficiency in interacting with culturally diverse employee population.

EXPERIENCE & EDUCATIONAL REQUIREMENTS 

+2 year of experience in a Quality Technician II position or Minimum 6 months internship in the medical industry in functions related to Quality. Quality leadership experience working in a manufacturing environment. High School Diploma. Certificate or Technical degree related to Quality (or with + 50 % of the technical degree completed. ISO 13485 auditor accreditation is desirable. Competencies Values: Integrity, Accountability, Inclusion, Innovation, Teamwork