Engineer - Process

Role: Process Engineer responsible for ensuring reliable operation and qualification of manufacturing equipment in a GMP environment, supporting pharmaceutical production. Responsibilities include safety management, system validation, troubleshooting, process optimization, and cross-functional collaboration with operations, maintenance, and vendors. The engineer ensures systems are in-control, compliant, and capable of meeting safety, quality, and productivity standards, with a focus on equipment reliability and continuous improvement. Requirements: Bachelor's degree in Mechanical or Electrical Engineering; 1+ years’ experience in regulated manufacturing, preferably pharmaceutical or parenteral. Skills include understanding of GMP, validation, troubleshooting, and process improvement; strong communication skills; and experience with commissioning, qualification, and cGMP regulations. Preferred qualifications include experience in pharmaceutical manufacturing, validation, and cross-functional project delivery. High-Value: GMP pharmaceutical manufacturing, parenteral/packaging processes, equipment validation, safety culture, process troubleshooting, continuous improvement. Work setup: 8-hour dayshift, with extended hours and occasional travel for project activities.