Hi, how can we deal with the verification of the internal auditors competence in a small company, with 2 auditors?
QS 9000 APQP and PDCA in ISO 9001
My question is about the Plan, Do, Check and Act in the New ISO 9001:2015 standard. Is it like the APQP that was in the old QS 9000 standard?
Maintaining ISO 9001 and TS 16949
Should an Industry need to hold ISO9001 AND TS 16949 together? Or having TS implies to have ISO 9001 also.
Defining the scope of internal laboratory
How do you handle the Lab Scope for the internal lab that only does measurement and some basic calibration. Rest is outsourced?
ISO 9001 vs IATF 16949 transition
Our Company was TS 16949 and now we a transiting to ISO:9001:2015. The question has keep up do we need to keep APQP for new product. I have been ask to to provide information on the requirement. I responded the section 8.2.3 thru 220.127.116.11.
Required documentation vs documented process
I'd like to know of a difference of wording "Required documentation" and " Required documented processes."
The procedure manual, context and interested parties
What exactly require in procedure manual, as per clauses it is mandatory to write a procedure for all clauses? I don't understand how to make procedure manual, how to identify the context of the organization, how to identify internal n external issues and interested parties.
Special approval of FMEA for product safety
What is the difference between special approval for FMEA and special approval of FMEA in my factory? We made FMEA for each product is those FMEAs enough for the clause of product safety 18.104.22.168?
Product safety requirements when there are no such requirements
In IATF clause 22.214.171.124 -- don't understand product safety thing. We make small washers, third tier supplier, nothing to do with product safety. How do I satisfy this need? I am sure others might be in similar situation.
Evidence of awareness of the core tools
Is it mandatory to maintain record of core tools awareness evidence of internal auditors?