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1+ months

Senior Verification & Validation Engineer

Scugog, ON L0B
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Senior Verification & Validation Engineer


Caesarea, Haifa, Israel

Requisition #:


Post Date:

Dec 16, 2020

**Careers that Change Lives**

Mazor Robotics Ltd, a Medtronic company since December 2018, is a global pioneer of robotics technology for use during spinal procedures. Our site is now focused on developing and supplying high quality, innovative surgical planning and robotic solutions/products. Join us in working at a local and friendly site with global impact and reach.

Together, we can confront the challenges that will change the face of healthcare.

Join us for a career that changes lives.

**A Day in the Life**

As a Senior VV Engineer you will be working in a multi-disciplinary environment with software, control, electrical and mechanical engineers. You will be planning and performing VV tests for highly complex electro-mechanical medical devices.

As part of your day to day you will:

Act as VV and Testing Tech Lead of NPI projects.

Review specifications and technical design documents to provide timely and meaningful feedback.

Designs, develops, and implements testing methods and equipment.

Creates detailed, comprehensive and well-structured VV test plans, protocols and reports.

Designs, develops and executes verification and validation tests

Plans and arranges the labor, schedules, and equipment required for testing and evaluating standard and special devices.

Identifies, records, documents and tracks defects during testing.

Provides test area with parameters for sample testing and specifies tests to be performed.

Interacts closely with Development Engineers.

Supports QA aspects of technology transfer of developed manufacturing processes and new product development from RD to manufacturing environment

**Must Haves:**

BSc. degree in Mechanical or Electrical engineering.

5-7 Years of proven experience in HW VV tasks including writing executing test plans and protocols, in medical device industry with a strong emphasis on quality assurance, problem solving, along with written and verbal skills.

Formal and practical knowledge of testing methodologies.

Good documentation skills and ability to communicate effectively at all levels of the organization

Very good English skills (read and write and speak)

Experience working with offshore sites/teams

Strong technical orientation for understanding multi-disciplined systems

**Nice Haves:**

Experience with CE and FDA regulations

Experience with validation processes

Software PLM (WCL), ALM (Qpack)

Familiar with Medical Device Quality Systems, ISO 13485:2003 and CFR21 Part 820.

**About Medtronic**

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. Lets work together to address universal healthcare needs and improve patients lives. Help us shape the future.
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.


Posted: 2020-12-24 Expires: 2021-03-28
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Scugog, ON L0B

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