J
JaimeB
First of all, I would like to thank all who answer questions at the Cove, I have found this forum to be invaluable as I acclimate myself to my new position as the QMS coordinator at a small aerospace engineering firm.
A little background...I started this position a week ago. I was hired more for my writing and organizational abilities than for my knowledge of QMS or AS9100. Prior to this position, my experience was mainly in the field of mid-size call center management for an ISO9000 certified medical device manufacturer. As such, I have participated in several internal audits and was responsible for ensuring those who reported to me were adhering to the SOPs that applied to our group.
That said, I am feeling a bit overwhelmed. Before I arrived, my new employer hired a consulting firm who basically churned out a canned QM and 17 canned procedures. In additon, the procedures they created seem to cover more of what the consulting firm thought should be done, rather than what we actually are doing.
I guess the reason for my post is two fold - In your opinions, is it possible for someone with a limited background in QMS to be successful in a role such as mine? What advice can you offer me on how to tackle this? Any suggestions of free online training that would be helpful?
I know this is kind of a lame post, but I really could use some reassurance and/or advice.
Thank you in advance for your consideration.
A little background...I started this position a week ago. I was hired more for my writing and organizational abilities than for my knowledge of QMS or AS9100. Prior to this position, my experience was mainly in the field of mid-size call center management for an ISO9000 certified medical device manufacturer. As such, I have participated in several internal audits and was responsible for ensuring those who reported to me were adhering to the SOPs that applied to our group.
That said, I am feeling a bit overwhelmed. Before I arrived, my new employer hired a consulting firm who basically churned out a canned QM and 17 canned procedures. In additon, the procedures they created seem to cover more of what the consulting firm thought should be done, rather than what we actually are doing.
I guess the reason for my post is two fold - In your opinions, is it possible for someone with a limited background in QMS to be successful in a role such as mine? What advice can you offer me on how to tackle this? Any suggestions of free online training that would be helpful?
I know this is kind of a lame post, but I really could use some reassurance and/or advice.
Thank you in advance for your consideration.