53 empleos en Mexicali, Baja California de Calidad

Metrology Quality Technician - Aerostructuras

Collins Aerospace.

Basic Qualifications: -Currently studding Engineering or may have a Bachelors degree in related fields -At least 6 months of experience in a quality position using Buid IT, Polyworks, VxElements -Knowledge of measurement tools and equipment Laser Tracker, Faro Arm, Creaform scan, CMM. -Engineering Drawing interpretation GD&T. CATIA -Knowledge in 365 office -Effective communication -Teamwork -Personnel management / leadership -English 70% -Proficient in excel Job Responsibilities: -Evaluates Collins Aerospace or supplier products and processes. Participates in cross-functional efforts to ensure proper corrective actions are implemented in a timely manner. -Maintains quality data records, compiles information, and prepares reports for internal and external customers. -Provides support to manufacturing operations in the review of products and of engineering and manufacturing processes, including First Article inspections. -Performs product audits in accordance with Collins Aerospace/customer/industry standards, reports results, assigns and monitors follow-up actions. -Performs duties required by the Quality Management System. -Maintains Inspection Stamp control for production employees. -Applies quality standards for receiving, in-process and final inspection in accordance with Collins Aerospace and contractual requirements. -Maintains equipment calibration and tooling tracking systems. -Functional areas: Quality Assurance, Quality System Validation, Supply Chain Quality Assurance or Materials Verification Aplica en el siguiente link: https://globalhr.wd5.myworkdayjobs.com/REC_RTX_Ext_Gateway/job/LOC5012-UTAS---GAM-Venustiano-Carranza--238-Desarrollo-Industrial-Colorado-Mexicali-21397-Mexico/Tcnico-de-Calidad-1st-Shift---On-site_01693648-1 Dirección: Calz. Venustiano Carranza #238 Col. Robledo

Junio 14 2024 en Mexicali

Risk Management Engineer

Intuitive Surgical, S. de R.L de C.V.

Skill/Job Requirements: Competency Requirements: In order to adequately perform the responsibilities of this position the individual must possess: English Level:  High (Good writing and speaking skills in English) Education: Bachelor degree in electrical, mechanical or system engineering, life sciences, mathematics, or physics. Advanced degree is a bonus. Able to navigate quality and compliance system with minimal oversight on individual projects. Basic knowledge of CFR 21 820/ ISO 13485 requirements for making process or design changes. Understands product risks, able to work with design and quality engineers to update risk documents. Understands Design Controls, Change Controls, Product, and Engineering Processes. Uses data to quantitatively communicate problem or issue. Basic functionality in PowerPoint Understands typical Excel data analysis operations (bonus for Vlookup, Pivot table and pivot chart functions). Works with Peers to understand and document issues. Operates with minimal oversight for basic problems or assignments, and escalates appropriately for issues requiring clarification. Preferred: 1 to 3years of working experience in a medical device company Experience with Agile/ACCS, TrackWise, or other electronic documentation systems (desired) Participation in internal / external audits conducted Aware of SPC & Six Sigma methodology and tools (e.g. uses DMAIC process and basic tools such as 5 Why's, control charts, fishbone diagram). Personality Requirements Able to cope with changes and uncertainties; and handle associated risks comfortably. Ask questions and don’t stop at the first answer. Analyze deeply to ensure the solution is the most effective solution. Brings unpleasant facts to discussion, does not hold back information. Driven by results. Fully supports team decision, even if he/she disagrees with the decision.

Junio 14 2024 en Mexicali

Product Release Associate

Intuitive Surgical, S. de R.L de C.V.

Skills, Experience, Education, & Training: ·       High School, Technical Diploma or Bachelor’s degree. ·       8 months to 1 year relevant experience in QA/QC role within a medical device company. ·       Ability to read English, read and comprehend instructions, write short correspondences and memos, complete quality documentation in English and Spanish, effectively present information in one on one and small group situations involving employees, supervisors or engineers. ·       Demonstrated understanding or aptitude to understand Medical Device QMS requirements and regulatory requirements. ·       Demonstrated ability to be a quick learner and understand complex products and processes. ·       Exceptional analytical, problem-solving, and root-cause analysis skills. ·       Integrity: Accepting and adhering to high ethical, moral, and personal values in decisions, communications, actions and when dealing with others. ·       Demonstrated ability to work independently and with minimal supervision, multi-task, and handle tasks with competing priorities effectively. ·       Very strong computer skills and experience with Windows operating system and Microsoft Office. ·       Ability to travel domestically and internationally. ·       Availability to work on different Shifts as needed. ·       Demonstrated interest in Medical devices, anatomy, surgery and the medical field. ·       Experience with Agile/ACCS and SAP or other electronic documentation systems. English 70%

Junio 14 2024 en Mexicali

Regulatory, Post Market Surveillance Analyst

Intuitive Surgical, S. de R.L de C.V.

Education: degree in engineering, life science, or equivalent Experience: 2+ years of experience in medical device field. English 90% (mandatory) Working knowledge and understanding with Medical Device Complaint files and quality record documentation Working knowledge and understanding of Regulatory reporting requirements for Medical Devices (US FDA requirements, EU MDD requirements, etc.). Skills: The following skills are required for this position: Demonstrate strong written and verbal communication skills Strong computer skills (Excel, Word, PowerPoint, database) Efficient independent worker with ability to focus Attention to detail Demonstrate cross functional communication skills in email and in person Excellent organizational and analytical skills Ability to handle and manage workload independently Prioritize numerous activities in a rapid paced environment Contribute to team-oriented tasks Strong analytical skills Strong interpersonal and decision-making skills Competency / Training: The following competencies are essential for this position: Firm understanding of Regulatory reporting requirements for Medical Devices and complaint system and process requirements. Firm understanding of quality records requirements and how they apply to complaint files. Familiarity with world-wide regulatory reporting requirements. Able to make decisions quickly using information at hand and evaluate the need to obtain clarification and direction when necessary.

Junio 14 2024 en Mexicali