Engineering Supervisor

at  Medtronic

Ciudad Juárez, Chih., Mexico -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate24 Jun, 2024Not Specified28 Mar, 20242 year(s) or aboveQsr,Process Capability,Histograms,Gr&R,Excel,IsoNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

MUST HAVE: MINIMUM REQUIREMENTS

Industrial Engineer or Completed Professional Career
2 years minimum of experience as a Quality Engineer in the manufacturing environment, preferably of medical products.
Bilingual: 70%
Problem resolution and use of quality tools:
(Pareto, Brainstorming, Histograms, Process Capability, GR&R, Process Mapping, FMEA)
Knowledge of cGMP, ISO 13485; 2016 & QSR
Computer packages (Excel, Word, Power Point)
Nice to Have

ABOUT MEDTRONIC

Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.
Physical Job Requirements
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America

Responsibilities:

  • Plans, directs and implements all aspects of the company’s design and development of new medical device products or software systems.
  • May develop, evaluate, implement and maintain technical quality assurance and control systems or reliability systems and standards pertaining to materials, techniques, or company products.
  • Oversees the investigation and evaluation of existing technologies.
  • Guides the conceptualization of new methodologies, materials, machines, processes or products.
  • Directs the development of new concepts from initial design to market release.
  • Manages feasibility studies of the design to determine if capable of functioning as intended.
  • Monitors documentation maintenance throughout all phases of research and development.
  • Organizes the coordination of activities with outside suppliers and consultants to ensure timely delivery.
  • Selects, develops and evaluates personnel to ensure the efficient operation of the function


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Other Industry

IT Software - Other

Other

Graduate

Proficient

1

Ciudad Juárez, Chih., Mexico