Job Description SummaryThe Quality Assurance Engineer is responsible for providing guidance for engineering process support in accordance with documented procedures and practices.
In addition, the QE will need to develop and maintain systems, procedures, and processes to ensure fulfillment of internal and external requirements based on medical device standard ISO 13485. Ensures compliance to applicable standards and regulations. Has knowledge of best practices including vast knowledge in design & development methodologies.

Job Description

Roles and Responsibilities

We are looking for an enthusiastic and passionate Quality Assurance engineer to take a central role in our QA/RA team and support QMS and Design Controls activities.

As part of your role, you will:

Ensure the product is developed per a well-defined Design Controls process and procedure, from planning, to design and implementation, verification and validation, and finally design transfer to manufacturing. Make sure everything is documented, risks are mitigated, and traceability is established end-to-endSupport product development at all project phases, ensure development and design reviews (FDRs, TDRs, etc.)Support requirements initiation / rationales for requirements and testing (e.g., testing covers all requirements, and applicable configuration)Manage DHF activities and documentation, initiate, and review program deliverables and ensure that the deliverables are in compliance with company’s QMS, applicable standards and regulationsHandle and coordinate Risk Management activities (experience with ISO 14971 preferred)Handle QMS activities at the site including quality trainings, internal audits, quality management reviews and implementation process of global proceduresTake a leading role in external audits and internal auditsInterfaces with R&D, Regulatory Affairs, Clinical, Process Development and Manufacturing functions in a project team environmentUtilizes in-depth knowledge of a discipline and analytical thinking to execute policy/strategy. Basic knowledge of related job disciplines.Acts as a resource for colleagues with less experience. May lead local improvement projects and be part of global GE projects/initiatives. Explains information; developing skills to bring team members to consensus around topics within field. Conveys performance expectations and may handle sensitive issues.Jobs at this level function with some autonomy but are subject to functional practices and precedents or are covered by well-defined policies or review of end results. The job allows modification of procedures and practices covering work as long as the end results meet standards of acceptability (quality, volume, timeliness etc.).Uses judgment and has the ability to propose different solutions outside of set parameters to address more complicated, day-to-day problems. Has ability to prioritize information for data analysis. Uses technical experience and analytical thinking. Uses multiple internal and limited external sources outside of own team to arrive at decisions.

Requirements

B.Sc in Mechanical / Biomedical / or similar from a known academic institution.3-5   years of hands-on experience in a similar role in a multi-disciplinary medical device company (Hardware, Software, Mechanics), working according to the MDR and CFR 21 Part 820, ISO 13485 regulatory requirements, ISO 14971, IEC 62304, IEC 60601R&D experience in a multi-disciplinary company – advantageDemonstrate in depth experience and understanding of product development lifecycle and design control activities (including Risk Management, design input/output, verification and validation etc.) in a medical device environmentExperience with cross functional project teamwork and collaboration with R&D, RA, QA, Product, Program, and Operations team membersStrong interpersonal, written, and verbal communication skills (Hebrew & English)3-5   years working experience in Quality Engineering in Medical Device company.Strong oral and written communication skills. Demonstrated ability to analyze and resolve complex problems. Ability to document, plan and established design documents.Demonstrated understanding of product development lifecycles, design changes and document change control, process verification and validation methodologies, design transfer, and servicing in a medical device environment.Ability to multi-task & handle tasks with competing priorities effectivelyExcellent interpersonal relationship – team player and team -oriented.Demonstrated collaboration, negotiation & conflict resolution skills.Demonstrated knowledge of Quality Management System tools, continuous improvement methodologies & in-depth understanding of site level products & related processes

GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.

GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity. 

 

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

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Additional Information

The job is open to men and women equally

Relocation Assistance Provided: No