Sr Process Engineer

Role: Engineering subject matter expert supporting biopharmaceutical manufacturing processes, including cell culture, harvest, purification, and utilities systems. Responsibilities: manage system lifecycle from design, installation, qualification, maintenance, to decommissioning; develop engineering deliverables (P&IDs, specifications); lead system qualification, FAT, commissioning, deviations, and CAPEX projects (up to $5M); ensure GMP compliance, process reliability, and performance; support capacity planning and troubleshooting. Requirements: Bachelor's in Engineering, 3+ years in pharma/biotech manufacturing; knowledge of bioprocess systems (bioreactors, chromatography, CIP, autoclaves, utilities); experience with regulatory and GMP environments; familiarity with automation, instrumentation, data systems (SQL, scripting preferred); strong project management, troubleshooting, and cross-functional collaboration skills. Preferred: Professional Engineer license, experience supporting large capital projects, automation controls. High-Value: bioprocess manufacturing, GMP, qualification protocols, equipment validation, manufacturing support, cross-functional project management. Work setup: on-site in Brooklyn Park, MN; travel up to 25%; includes facility walkdowns, PPE use, occasional ladder work.