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confusedkid
Hi Everyone. My company is divided into two sections: (1) a medical device manufacturing company exclusively for the (2) CLIA certified clinical lab. My company is not FDA reg or ISO certified and we are striving to obtain certification but I fear it won't be completed for awhile. We have some systems in place but not all. I've been here for 3 years. I have a total of 4 years of experience in quality and I've taken ISO 13485 training classes. If I look for another job, will it hurt me that my company is not FDA/ISO regulated? What can I write in my resume? Thanks!