Are you interested in working for a global company where you can work across functions and on a wide-variety of projects? As a member of Stryker's RA/QA team, that is exactly what you will do! Here, we provide our RA/QA team the opportunity to learn new things, as well as endless growth opportunities! If you are interested in working at one of the World’s Best Workplaces, apply now !
Need another reason to apply? Here are 10 reasons to join our Regulatory Affairs/Quality Assurance team: https://www.strykercareersblog.com/post/10-reasons-to-join-strykers-regulatory-affairs-team
- Review DHRs
- Scan all the device history records (DHR)
- Prepare indexes for DHRs before sending hardcopies to the archive
- Prepare approved documents for implementation in the QMS (stamp and scan)
- Assist with administrative activities
- Perform inspections, checks, tests and sampling procedures of incoming materials, parts and components.
- Perform in-process and final inspection
- Perform inspection before shipment
- Handling and maintenance of documents archive
- Clean room microbial sampling
- Review and approval of part specifications documents
- Qualifications required:
- 12 Years of schooling
- Basic computer skills - Microsoft Office applications
- Hebrew proficiency/ English - an advantage
- Strong interpersonal skills and the ability to effectively communicate with employees at all levels of the organization.
About Stryker
Stryker is one of the world’s leading medical technology companies and, together with our customers, is driven to make healthcare better.
The company offers innovative products and services in Medical and Surgical, Neurotechnology, Orthopedics, and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 100 million patients annually.
More information is available at stryker.com
$ads={1}