Equipment Engineering Manager - Mexicali, México - Intuitive

Intuitive

Empresa verificada

Mexicali, México

hace 2 semanas

Publicado por:

Rodrigo Fernández

Reclutador de talento para beBee

Descripción

Descripción de la empresa:

At Intuitive, we are united behind our mission: we believe that mínimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.

As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference.

For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare's hardest challenges and advance what is possible.

Intuitive has been built by the efforts of great people from diverse backgrounds.

We believe great ideas can come from anywhere—we strive to foster an inclusive culture built around diversity of thought and mutual respect.

We lead with inclusion and empower our team members to do their best work as their most authentic selves.

Passionate people who want to make a difference drive our culture—our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real-world experiences to help us think in new ways.

We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential.

Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let's advance the world of mínimally invasive care.

Descripción del empleo:

The Equipment Engineer Manager will define and execute the strategy for the Equipment Engineering area.

Will manage and coordinate the resources and activities of the Equipment Engineering area by promoting the continuous improvement and introduction of new technologies to the production process, according to the procedures applicable to the engineering area and the standards indicated in ISO 13485, FDA 21 CFR820; ensuring the reliability of all the equipment used across all Mexicali sites.

To coordinate equipment engineering budget and to create/modify job descriptions.

To define and execute the strategy for the Equipment Engineering area that will promote the continuous improvement and support to released production processes for Instruments and Accessories to ensure reliability, cost, manufacturability and serviceability of all the Equipment in use across all Mexicali sites

To manage and coordinate the resources and activities of the Equipment Engineer area and provide mechanical and manufacturing support in accordance with FDA and ISO 13485 standard regulations.

Define budget of the department and execute as planned.

This position requires mínimal to no supervision.

Roles & Responsibilities:

Lead initiatives focused on yield improvement, material cost reduction, and equipment capacity reliability and improvement.
Evaluate and challenge mechanism designs for equipment reliability, serviceability and manufacturability. Provide suggested change proposals.
Follow up on the solution of defects in process by equipment (EE's), ensuring corrective and preventive actions are in place to avoid recurrence.
Ensure that the equipment meets the required parameters and specifications, avoiding variations in the manufacturing process.
Create budget estimates for tooling, test equipment, and prototype designs.
Provide technical support analyzing and /or performing failure analysis
Take responsibility for developing and maintaining compliance with the quality system.
Evaluate and select suppliers for mechanical parts. Help resolve supplier quality issues.
Must possess strong communication skills to interface with suppliers, product development, planning, purchasing, regulatory, inspection, customer support and clinical marketing organizations.
Performs other duties as required.
Travel: Position may require 510% travel, primarily within U.S.

Requisitos:

Skills, Experience, Education, & Training:

Required:

BS degree in Mechanical Engineering, Electronic Engineering or equivalent.
Demonstrate Mechanical and/or Process Engineering ability.
Demonstrate ability for failure analysis and continuous improvement.
Minimum 3 years mechanical, maintenance or manufacturing engineering supervision experience with Mid/high volume complex manufacturing processes.
3 to 5 years of proven experience working as Manager in an equipment, maintenance or manufacturing related position, supporting production processes with significant mechanical content.
Highly experienced in NPI and transferences.
High English spoken skills (bilingual).
Equipment and software validation experience in medical industry regulations (IQ, OQ, PQ).

Preferred:

MS degree in an Engineering discipline (Mechanical Engineering, Electronic Engineering are preferred)
Project management experience is highly desirable.
Prior experience working in FDA/ISO 13485 medical device manufacturing environment.