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Sustaining engineer, material cip (tecate)

Tecate, B.C.
Teleflex
Publicada el 29 octubre
Descripción

Sustaining Engineer, Material CIP

**Date:** Oct 27, 2025

**Location:** Tecate, BCN, MX

**Company:** Teleflex

**About Teleflex Incorporated**

As a integral provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.

Teleflex is the home of Arrow, Barrigel, Deknatel, QuikClot, LMA, Pilling, Rüsch, UroLift and Weck - trusted brands united by a common sense of purpose.

At Teleflex, we are empowering the future of healthcare. For more information, please visit **teleflex.com**.

**Global Operations**

Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients' lives.

**Position Summary**

Teleflex is strengthening its capabilities to reduce material costs, reverse rising industry pressures, andenhance product margins. In this exciting new role, you'll be responsible for generating and executingcost improvement projects (CIPs) within our Global Procurement team. You'll drive meaningful impactby leading initiatives such as supplier changes, process development, and supplier improvementscollaborating closely with Commercial Sustaining Engineering to deliver real, measurable savings.Success in this role calls for strong project management, a solid understanding of development andmanufacturing, and a commitment to quality, compliance, and customer needs.

**Principal Responsibilities**

- Conducting value analysis and value engineering studies.

- Identifying cost-saving opportunities in product design and production processes.

- Evaluating the functionality of products and services to ensure they meet customer needs while being cost-effective.

- Developing detailed reports on value engineering findings and presenting them to senior management.

- Conducting cost-benefit analyses to support decision-making processes.

- Recommending design changes to enhance the value of products or services.

- Tracking and reporting progress on value engineering projects.

- Ensuring compliance with industry standards and regulations.

- Draft and route project Charters, identifying the required deliverables per local and global procedures, as well as governing regulations, with moderate guidance.

- Interface with cross functional teams to track project deliverables, responsibility, and progress.

- Utilize available data to build timelines, task trackers, risk registers, meeting cadences, etc. based on knowledge of project management processes.

**Education / Experience Requirements**

+ Bachelor's Degree in a related engineering, administration or other relevant field.

+ A minimum of5 years of experience in medical device, regulated industry, or related field executing a sustaining, manufacturing, or process engineering role, value engineering, cost engineering, or a related role preferably in a relevant industry.

**Specialized Skills / Other Requirements**

+ Bilingual (fluent in Spanish and English).

+ Proficiency in root cause analysis methodologies.

+ Experience with statistical process control (SPC) and data analysis.

+ Knowledge of manufacturing processes and design for manufacturability (DFM).

+ Experience with ISO Standards (ISO 9001, ISO 62366, ISO 13485, ISO 14971).

+ International Medical Device Regulations (MDR, FDA, COFEPRIS, Others).

+ Project Management skills (Risk Analysis, Scheduling, Planning, Data Analysis, Reporting).

+ Value Stream Mapping.

+ Cost-Benefit analysis.

+ Strong analytical, financial modeling, and quantitative skills, with a focus on maximizing savings.

_At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front._

_Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or_ _talent@teleflex.com_ _._

_Teleflex, the Teleflex logo, Arrow, Barrigel, Deknatel, QuikClot, LMA, Pilling, Rüsch, UroLift and Weck are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries._

_© 2025 Teleflex Incorporated. All rights reserved._

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