I concur with every one of the members in the posts above in regards to the part of PM and his or her obligations of Quality Assurance. Quality Assurance duty is a gigantic undertaking inside Quality in a medicinal gadget industry. Few errands that I will be dependable as far as info are to make a point to get finish subtle elements of the assembling procedure before settling the due date. Moreover, I would need to meet with the topic master (SME) to ensure investigate has been done totally on the venture. Also, as far as yield, I would need to ensure all the right documentation has been done and closed down by the fitting supervisor. In the therapeutic business, documentation is more essential and is required by the FDA to keep up record of generation.