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Salary
≈ $63k – $138k per year (Estimated)
Location
In office (Yokneam)
Seniority
Middle · 3+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 8, 2026. First seen by Alion on Oct 6, 2026. Medtronic scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Medtronic is one of the largest medical device manufacturers in the world, founded in a Minneapolis garage in 1949 as a repair shop for hospital equipment before building the first wearable cardiac pacemaker. Its portfolio now spans cardiac rhythm devices, heart valves, neuromodulation and neurosurgery, surgical stapling and robotics, spinal implants and diabetes management systems sold in more than one hundred and fifty countries. The company is legally domiciled in Ireland after its 2015 combination with Covidien, while its operational headquarters and most of its research remain in Minnesota.

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

Join our engineering team as a Process Engineer and help drive meaningful improvements across our manufacturing operations. In this role, you will lead opportunities to enhance efficiency, quality, and safety while working closely with cross-functional teams to solve problems and optimize processes. This is an exciting opportunity for a motivated engineer who enjoys hands-on impact, continuous improvement, and contributing to a high-performing environment. If you are looking for a role where your ideas can make a real difference, we encourage you to apply.

This position is on-site working based at Medtronic Yokneam. You will report to the engineering manager and collaborate regularly with teams across production, quality, maintenance, and operations. Some travel may be required to support other sites, project work, or training initiatives. The role offers the chance to work in a fast-paced environment with strong opportunities for learning, development, and career growth.

Primary Responsibilities

  • Responsible for all manufacturing processes on production floor, pFMEA, Equipment URS, Working instructions, test methods, Support production training, Define Packaging instructions; Ensures processes and procedures are following regulations; Monitors documentation maintenance throughout all phases of product lifecycle.
  • Project management skills, Responsible for timelines, Scop of work, Budget.
  • Implement jigs, fixtures, and other manufacturing support tools for medical device assembly and testing.
  • Improve manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling; Review arrangement of machines within plant facilities to ensure most efficient and productive layout.
  • Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance.
  • Support manufacturing processes that are applicable to statistical process control, and may develop those techniques; Issue specification requirements to best utilize equipment and manufacturing techniques.
  • Drives a continuous improvement mindset by engraining and improving the MPS (Medtronic Performance System) methodologies in the day-to-day; Execute Improvement in Yokneam Operations KPIs (Yields, Scrap, Quality, Safety, OEE).
  • Acts as a partner with mainly production and Quality operations and other functions in Operations and R&D sustain team.

Required Qualifications

  • B.Sc. degree in Mechanical Engineering or another relevant manufacturing-focused engineering field.
  • Minimum of 3 years of experience in manufacturing engineering within the medical device, pharmaceutical, or process industries.
  • Written and verbal communication skills in English.
  • Strong problem-solving and execution abilities.
  • Proactive approach; Full responsibility for the delivery of outputs, including supporting documentation; a "Big-picture" mindset. including influence and communication skills.

Preferred Qualifications

  • Certifications such as Six Sigma/Green belt or Lead Auditor (ISO 13485).
  • Sold work skills.

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.

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 @medtronic.com email addresses.

Medtronic 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 [email protected].

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.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).
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