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 Regulatory Affairs 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 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
12 Years of schooling
Basic computer skills
Strong interpersonal skills and the ability to effectively communicate with employees at all levels of the organization.
Know someone at Stryker?
Be sure to have them submit you as a referral prior to applying for this position.
Learn more about our employee referral program at https://careers.stryker.com/referrals/
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