Ingeniero de Manufactura I

MX3 MMJ, S.A. de C.V.; Ciudad Juárez; On-site; MXN 350,000 - 520,000; Full time

Job summary

Medtronic in Ciudad Juárez, Mexico, is hiring a Manufacturing Engineer I to support calibration, equipment qualification, validation, and production activities in a regulated environment. This on-site role collaborates with Manufacturing, Quality, Operations and other engineering teams to ensure compliant and reliable equipment and processes.

The ideal candidate has hands-on experience with IQ, OQ, PQ and TMV, strong analytical skills, and the ability to work across functions.

Qualifications

• Bachelor’s degree in Engineering or related field.
• Hands-on experience in manufacturing engineering, validation, quality engineering, or calibration environment.
• Experience with IQ, OQ, and PQ validation.
• Understanding of manufacturing equipment and measurement systems.
• Strong analytical and problem‑solving skills.
• Ability to work effectively in a cross‑functional manufacturing environment.
• Good written and verbal communication; English proficiency.

Responsibilities

• Support calibration activities for manufacturing equipment.
• Develop, execute, and document IQ/OQ/PQ validation protocols.
• Support Test 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 structured root cause analysis and problem‑solving methodologies.
• Support corrective and preventive actions related to equipment or process performance.
• Participate in risk 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.

Skills

Analytical and problem-solving skills

Cross-functional collaboration

Communication skills

English proficiency

On-site manufacturing environment

Education

Bachelor’s degree in Engineering or related field

Tools

IQ/OQ/PQ protocols

TMV validation

Minitab

Measurement systems analysis (MSA)

Job description

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 Life

We are seeking a Manufacturing Engineer I to join our Calibration team at our manufacturing site in Ciudad 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 with equipment and/or process validation, including IQ, 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 is 100% onsite and requires regular interaction with manufacturing operations and production equipment.

Key Responsibilities

• Support calibration activities for manufacturing, inspection, measurement, and test equipment.
• Support the development, execution, and documentation of equipment qualification and validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
• Support Test 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 structured root cause analysis and problem‑solving methodologies.
• Support corrective and preventive actions related to equipment or process performance.
• Participate in risk 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 Requirements

• Bachelor’s degree in Engineering or a related technical/scientific discipline.
• Previous experience or demonstrated knowledge in a manufacturing engineering, validation, quality engineering, or calibration environment.
• Hands‑on knowledge of equipment and/or process validation, particularly IQ, 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 proficiency sufficient to work with technical documentation and global engineering teams.
• Ability to work onsite in Ciudad Juárez, Chihuahua, Mexico.

Preferred Qualifications

• Experience in medical device manufacturing or another highly regulated manufacturing environment.
• Knowledge of ISO 13485 and regulated medical‑device manufacturing requirements.
• These are also identified as preferred capabilities in the internal Manufacturing Engineer profile.
• Experience preparing or executing IQ/OQ/PQ validation protocols and reports.
• Experience with Test Method Validation (TMV).
• Knowledge of measurement systems, calibration principles, MSA, and Gage R&R.
• Familiarity with pFMEA, CAPA, nonconformance investigations, change control, and root cause analysis.
• Experience using statistical tools such as Minitab for process or validation analysis.
• Exposure to equipment qualification, preventive maintenance, metrology, or calibration programs.
• Knowledge of GD&T and interpretation of engineering drawings is a plus.

Physical Job Requirements

The 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.

Benefits & Compensation

Medtronic offers a competitive Salary and flexible 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.

This position is eligible for a short‑term incentive called the Medtronic Incentive Plan (MIP).

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. We change lives. Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That’s who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives. We build extraordinary solutions as one team. With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough. This life‑changing career is yours to engineer. By bringing your ambitious ideas, unique perspective and contributions, you will… Build a better future, amplifying your impact on the causes that matter to you and the world Grow a career reflective of your passion and abilities Connect to a dynamic and inclusive culture that welcomes the challenge of life‑long learning

It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.

This employer participates in the federal E‑Verify program to confirm the identity and employment authorization of all newly hired employees.