Imagine how your ideas and expertise can change a patient’s life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You’ll bring your passion for problem solving and partner with various teams to influence decision-making for a product’s entire lifecycle. Your work will involve you optimizing product development to impact patients around the world with pioneering technology. 

How you will make an impact:

Perform visual, dimensional, and functional inspection across all components using a wide variety of all applicable tools and equipment such as magnifying lamp, microscope, vision inspection system (Keyence, OGP, ETC), etc. to ensure conformance with design specifications

Working independently at the highest levels of productivity

Perform functional testing of finished medical device products using both automated and manual valve testing equipment to ensure conformance with design specifications

Review, follow and perform job functions in compliance with established work instructions and adherence with SOPs, including recording traceable information on device history records and may enter information into ERP system.

Perform verification of manufacturing documents with component and device drawings, which may include Geometric Dimensioning and Tolerancing methodologies

May control inventory to ensure appropriate storage conditions and movement
 

What you’ll need (Required):

1-2 years of experience as Quality Control

Performing measurements with measurement systems such as Keyence or OGP

Ability to use applicable tools and equipment, hand eye coordination, and high manual dexterity

Medical device experience

Full understanding of applicable inspection procedures, including the ability to contribute to the development of procedures

Proficient in all inspection techniques for production inspection

Ability to clearly describe and convey nonconformance issues, and enter them into the system

Ability to program and contribute to the validation of automated test equipment

Ability to provide feedback on product defects and may follow through to establish resolution

What else we look for (Preferred): 

Strong communication skills and interpersonal relationship skills

Able to read, comprehend, speak, and write Hebrew

Good English language skills, including reading and writing

Good computer skills, required, including working knowledge of manufacturing software

Strict attention to detail

Must be able to work with minimum supervision

Work in a Team environment, and may work on inter-departmental teams

Adhere to Edwards Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing

Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control