Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the LifeWe are seeking aManufacturing Engineer Ito join ourCalibration teamat our manufacturing site inCiudad Juárez, Mexico.
This role will provide engineering support for calibration, equipment qualification, validation, and manufacturing activities in a regulated production environment. The ideal candidate will have hands-on experience withequipment and/or process validation , includingIQ, OQ, and PQ , and will work closely with Manufacturing, Quality, Operations, and other engineering functions to ensure equipment and processes remain compliant, capable, and reliable.
The position is100% onsiteand requires regular interaction with manufacturing operations and production equipment.
Key ResponsibilitiesSupportcalibration activities for manufacturing, inspection, measurement, and test equipment.
Support the development, execution, and documentation ofequipment qualification and validation protocols , includingInstallation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
SupportTest Method Validation (TMV)activities when applicable.
Develop, review, and maintain engineering documentation, protocols, reports, specifications, and manufacturing procedures.
Partner with Manufacturing, Quality, Operations, and technical teams to maintain validated equipment and processes.
Investigate equipment, calibration, process, and product issues using structuredroot cause analysis and problem-solving methodologies.
Support corrective and preventive actions related to equipment or process performance.
Participate inrisk assessments , including Process FMEA and other manufacturing risk-management activities.




Analyze manufacturing and equipment performance using statistical techniques and recommend improvements.
Support equipment changes, engineering changes, new equipment introduction, and manufacturing process improvements.
Ensure calibration and validation documentation is completed accurately and in accordance with applicable quality-system requirements.
Provide technical support directly on the manufacturing floor and help resolve issues impacting production, quality, or equipment performance.
Support continuous improvement initiatives focused on equipment reliability, process capability, compliance, and manufacturing efficiency.Minimum RequirementsBachelor’s degree in Engineeringor a related technical/scientific discipline.
Previous experience or demonstrated knowledge in amanufacturing engineering, validation, quality engineering, or calibration environment.
Hands-on knowledge ofequipment and/or process validation , particularlyIQ, OQ, and PQ.
Understanding of manufacturing equipment, measurement systems, and engineering documentation.
Strong analytical and problem-solving skills.
Ability to work effectively in a cross-functional manufacturing environment.
Good written and verbal communication skills.
English proficiencysufficient to work with technical documentation and global engineering teams.
Ability to workonsite in Ciudad Juárez, Chihuahua, Mexico.
Preferred QualificationsExperience inmedical device manufacturingor another highly regulated manufacturing environment.
Knowledge ofISO 13485and regulated medical-device manufacturing requirements. These are also identified as preferred capabilities in the internal Manufacturing Engineer profile.




Experience preparing or executingIQ/OQ/PQ validation protocols and reports.
Experience withTest Method Validation (TMV).
Knowledge ofmeasurement systems, calibration principles, MSA, and Gage R&R.;
Familiarity withp FMEA, CAPA, nonconformance investigations, change control, and root cause analysis.
Experience using statistical tools such asMinitabfor process or validation analysis.
Exposure to equipment qualification, preventive maintenance, metrology, or calibration programs.
Knowledge ofGD&T; and interpretation of engineering drawingsis a plusPhysical Job RequirementsThe above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official@ email dtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at.
Benefits & CompensationMedtronic offers a competitive Salary and adaptable Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

📌 Ingeniero De Manufactura I (Chihuahua)
🏢 Mx3 Cov - Mkdt Respiratory Mexico
📍 Chihuahua