Associate Regulatory Affairs Specialist

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life
Join our Regulatory Affairs team As an Associate Regulatory Affairs Specialist and be part of a purpose-driven community that is dedicated to improving patient care through high-quality, accessible, and affordable healthcare.

As an Associate Regulatory Affairs Specialist, you will play a key role in ensuring that Medtronic’s Pre-market regulatory activities in Israel align with both local Ministry of Health (AMAR) regulations and internal Medtronic standards. You’ll manage submissions, compliance tasks, and regulatory communications with a proactive, timely, and quality-focused approach.
You will work closely with global regulatory teams, operation units, and local stakeholders to bring life-changing technologies to patients in need, while maintaining the highest standards of safety and compliance.
This is a one-year contract position.

Responsibilities may include the following and other duties may be assigned:

Manage Pre-market activities, including submissions of new products, renewal and changes to the Israel Ministry of Health (Amar), in a timely and organized manner.
Provide strategic input from regulatory planning through to execution and follow-up of submissions.
Maintain Regulatory and technical documentation of the registered products required by the Israel Medical Device Law and MOH guidelines.
Support change submission processes, including preparation and tracking of the relevant medical device changes.
Perform Regulatory Operations activities, including coordination with Medtronic’s Global Trade Services (GTS) to release blocked orders and control product distribution in accordance with Distribution Control Compliance requirements. This includes ensuring compliance with legal regulations related to import/export, regulatory approvals, and quality standards.
Collaborate with global regulatory affairs teams and operation units to gather and analyze required information
Participate actively in cross-functional teams to meet timelines, resolve regulatory issues, and improve work processes.

Required Knowledge and Experience:

Bachelor’s degree in scientific discipline
Minimum of 2 years’ experience in regulatory affairs or quality assurance
Full professional proficiency in Hebrew and English
Experience in the medical device industry
Familiarity with local regulatory authorities and submission processes (e.g., AMAR)
Working knowledge of global regulatory frameworks including MDR (Medical Device Regulation)
Excellent attention to details, proactive approach and ability to work independently
High learning agility and ability to work under pressure
Strategic thinking and ownership of regulatory and quality initiatives

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. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

About Medtronic

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.