MSAT Process Engineer

The Process Validation Engineer plays a critical role in ensuring that manufacturing processes consistently produce products that meet predetermined quality standards and regulatory requirements. This position involves designing, executing, and documenting validation protocols to confirm that processes are robust, reliable, and capable of producing high-quality outputs. The engineer will collaborate closely with cross-functional teams including manufacturing, quality assurance, and research and development to identify process improvements and troubleshoot issues. A key outcome of this role is to provide comprehensive validation reports and technical documentation that support regulatory submissions and internal quality audits. Ultimately, the Process Validation Engineer ensures that manufacturing processes are optimized for efficiency, compliance, and product safety within the manufacturing environment in the United States. Required: 3-8 years of experience Life Sciences / Biopharmaceutical ManufacturingMSAT / Manufacturing Science Process Validation Upstream Processing Filtration Technologies (Filter Press, UF/DF, TFF) Process Development & Process Characterization DOE and Data Analysis GMP Manufacturing Support Technical Writing (SOPs, Protocols, Reports) Cross-Functional Manufacturing Support Required Skills: Protocol and report writing, validation/qualification documentation, engineering project execution, SOP authoring, data analysis, process documentation, cross-functional coordination #J-18808-Ljbffr ELIQUENT Life Sciences