I currently work in manufacturing and everything we do is review by Quality. Our department has a good relationship with QA who reviews our batch records. This may just be so due to the fact that manufacturing doesn’t really get to have much say in the process. Our process is defined by process development, we simply manufacture the produce and adhere to the standards that QA has for carrying out the process. However, when worked in Validation and was working on validating equipment for the GxP labs. That’s when I encountered a variety of problem with Quality in submitting the document that were needed to carry out the process. In my experience process development and research would defiantly have ore problems with Quality.