K
kreco
I have recently joined a mature company (30+) years in business and they have never been ISO or had any "real" work instructions. EVERYTHING here is loosely defined at best. The problem being is that for 25+ years the company had no real competition and it really didn't matter how badly they screwed up or how late a delivery was, the customer seriously had no choice to go elsewhere. But things have changed, we now have serious competition and because of our poor performance we have lost one customer after another. Financially the company is in BAD shape.
As the new QM I am in the very early stages of implementing ISO 9001, though we are about 7 months from full implementation. We do have routers that specifically state how the product should be manufactured, labeled, processed etc...so there should be NO questions on what is needed as far as product quality.
The problem is that we CONTINUE to see TONS of RMAs and repeat issues. Everyone here is so blase (pronounced blah-zay) about general policies, their workmanship etc. How in the world do you get an entire organization to get in gear and be accountable for their actions?
Here is a recent example: We are way behind on deliveries for a particular "set" that we ship out. There are 11 parts that complete one set and on top of not being able to keep up with delivery we are sending them nonconforming parts. Some parts are supposed to be marked with a dot and 2 weeks ago a shipment went out missing the dot. So I created a checklist for final inspection to use when inspecting these parts (this customer is the only customer that gets 100% final inspection, and currently it is actually 200% because one of the techs is new and I'm having the supervisor check her work) and even still this was missed. We were billed $800 for our customer's labor to mark the parts. So today I get another email from this customer and the most recent shipment that went out it happened again! So of course my boss will be coming down on me wanting to know HOW QA inspection could have missed this again! Obviously the parts should come to QA correct, but they are the safety net and I want them held accountable for the escape. I personally went down and checked inventory of all parts and found 2 more batches that were ready to ship out that weren't marked.:mg: I then made an inbox for incoming parts to this area specifically designated for those parts requiring the specific marking, to hopefully flag the orders and heighten awareness for them. So help me if I find one more batch I'm going to lose it!
I realize something in the process needs to change, but what else can I do to get QA to pay attention? We've talked about unpaid days off, but we are already behind in shipments so that won't help us.
This is just one example, but it seems like fixes don't stick. If you talk to people you just get "well that's just the <company name> way" . If you tell a supervisor to address something and communicate to their department that x process has changed, they don't tell them. People just don't seem to respond.
I know with the introduction to ISO things will improve, but you still have lots of people that I think will have a rough time with the new structure.
As the new QM I am in the very early stages of implementing ISO 9001, though we are about 7 months from full implementation. We do have routers that specifically state how the product should be manufactured, labeled, processed etc...so there should be NO questions on what is needed as far as product quality.
The problem is that we CONTINUE to see TONS of RMAs and repeat issues. Everyone here is so blase (pronounced blah-zay) about general policies, their workmanship etc. How in the world do you get an entire organization to get in gear and be accountable for their actions?
Here is a recent example: We are way behind on deliveries for a particular "set" that we ship out. There are 11 parts that complete one set and on top of not being able to keep up with delivery we are sending them nonconforming parts. Some parts are supposed to be marked with a dot and 2 weeks ago a shipment went out missing the dot. So I created a checklist for final inspection to use when inspecting these parts (this customer is the only customer that gets 100% final inspection, and currently it is actually 200% because one of the techs is new and I'm having the supervisor check her work) and even still this was missed. We were billed $800 for our customer's labor to mark the parts. So today I get another email from this customer and the most recent shipment that went out it happened again! So of course my boss will be coming down on me wanting to know HOW QA inspection could have missed this again! Obviously the parts should come to QA correct, but they are the safety net and I want them held accountable for the escape. I personally went down and checked inventory of all parts and found 2 more batches that were ready to ship out that weren't marked.:mg: I then made an inbox for incoming parts to this area specifically designated for those parts requiring the specific marking, to hopefully flag the orders and heighten awareness for them. So help me if I find one more batch I'm going to lose it!
I realize something in the process needs to change, but what else can I do to get QA to pay attention? We've talked about unpaid days off, but we are already behind in shipments so that won't help us.
This is just one example, but it seems like fixes don't stick. If you talk to people you just get "well that's just the <company name> way" . If you tell a supervisor to address something and communicate to their department that x process has changed, they don't tell them. People just don't seem to respond.
I know with the introduction to ISO things will improve, but you still have lots of people that I think will have a rough time with the new structure.
Off topic:
bla·sé (blä-zay)
adj.
1. Uninterested because of frequent exposure or indulgence.
2. Unconcerned; nonchalant: had a blasé attitude about housecleaning.
3. Very sophisticated.
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