6 years of experience in the position offered or related within pharmaceutical manufacturing. Must have 6 years of experience with providing engineering support and coordination with crossfunctional teams; performing design of experiments DOE, process validation, protocol execution, and commissioning of equipment including documentation; preparing user requirement specification, design specification, request for proposal, design review matrix, noncompliance punch list and commissioning summary; working with PLC, SCADA, and Human Machine Interface HMI tools; implementing Corporate and Global policies, procedures and standards; and applying knowledge of FDA, European Commission EudraLex, ICH and, Health Canada regulations and compliances.
Categories: eb3
0 Comments