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Quality Management System (QMS) Specialist, Caesarea, Israel

190004OV Requisition #
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Careers that Change Lives

As the Quality Management System (QMS) Specialist you will be responsible for leading and executing activities related to procedural document development and training. 

This position is a great opportunity to join a growing QA team in a global medical company. Suitable for candidates with relatively short experience in the industry for one or two years that wants to grow with us.

A Day in the Life

Duties and responsibilities may include, but are not limited to:

  • Coordinates the site procedures and work instructions routing, review, approval, distribution and maintenance.
  • Supports in preparation for Management reviews, internal and external audits .
  • Serves as a point of contact for the site employees in accessing/inquiring controlled documents.
  • Maps out annual QMS training plan, conducting organization-wide training needs assessment and identification of skills or knowledge gaps that need to be addressed.
  • Defines and maintains employees’ competence according to QMS requirements.
  • Maintains training database and records.
  • Evaluates training effectiveness and determines the impact of training on employee skills.
  • Monitors  Key Process Indicators (KPIs)
  • Organizes and maintains quality documents and records and tracks the document status.
  • Other duties may be assinged.

    Note: The following are meant to be representative but not necessarily all inclusive of the duties and responsibilities for this position title.

Must Haves
  • Bachelor’s or practical engineer degree, preferably  in a technical or scientific discipline.
  • 1-2 years of quality assurance/document control/training  in medical device or pharmaceutical industry
  • Basic knowledge of computer systems and commonly used software applications is mandatory.
  • High verbal and written communication skills (Hebrew and English)
Nice to Haves
  • Experience managing manual and electronic document management systems in a regulated pharmaceutical/medical device environment is preferred
  • Quality assurance certifications and courses
  • Understanding and knowledge of relevant regulations and standards FDA QSR, ISO 13485, MDD is preferred

Your Answer

Is this the position you were waiting for? Then please apply directly via the apply button!

About Medtronic
Mazor Robotics, Ltd., a Medtronic company .

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


Whatever your specialty or ambitions, you can make a difference at Medtronic - both in the lives of others and your career. Join us in our commitment to take healthcare Further, Together.

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Join us in our challenge to make global healthcare more affordable and accessible. Your insight and oversight will help us create solutions that change the world.

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The mission to improve access to healthcare globally is something we are all very proud to work hard toward achieving. Great people, fun atmosphere, big city salaries. The CEO is fantastic - he is a very clear communicator of the mission and is truly dedicating his life to achieving it.
Smart and committed coworkers. Mission driven. Good benefits. Good long term career opportunities. Company is large enough that you can always find interesting projects to work on.
Knowing that everyday your work helps to save lives makes it great place to work. Training on lean practices, quality and other. Excellent peers.


Be part of one of the world’s leading medical technologies and solutions companies.