Medline Industries, LP · USA
As a Validation Engineer at Medline Industries, LP, you will be responsible for the validation of facility utilities, equipment processes and cleaning for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210, 21 CFR 820, and other applicable regulatory requirements.
About the Role
Lead the authoring and executing of protocols to demonstrate that manufacturing and cleaning processes are executed with consistent quality and results.
Coach and assist Pharma Validation Engineers through the validation process.