I work at a manufacturing company that is headquartered in the USA with a production site in the EU. We are certified to ISO 9001 and the EU facility is certified to ISO 9001 and ISO 14001. EU has their own QMS and separate certification, HOWEVER, many of the core processes are shared and they utlize our ERP, CAR system, etc. Corporate objectives are handed down from US. Design work is primarily handled by us, with some local EU engineering work being done to capture customer requirements, validate product, etc. There are local variations to some processes (some of which we're working to standardize with HQ, some would be wise to leave alone), and of course different regulatory requirements.
Looking for a quick sanity check. Would like to align the systems so that we have one QMS while allowing them to maintain a separate certification as not to put our cert in jeopardy if they blow an audit.
Thanks!
Looking for a quick sanity check. Would like to align the systems so that we have one QMS while allowing them to maintain a separate certification as not to put our cert in jeopardy if they blow an audit.
Thanks!