We are looking for someone to directly support the IOPQ executions of our Cell Shuttle and Subsystems. This is a fast-paced role at the forefront of automated manufacturing technology. When schedule permits, you’ll also have the opportunity to support our broader GMP and QC equipment.
What the role involves:
• Protocol Execution: Direct, hands-on execution and documentation of IQ, OQ, and PQ protocols, summary reports, and discrepancy reports.
• Automated Systems: Working closely with SCADA, PLC, and HMI systems within a highly automated environment.
• Compliance: Upholding strict GMP/GDP practices and navigating QMS platforms (like TrackWise) to manage discrepancies.
What we are looking for:
• 3–5+ years of dedicated Validation experience in a regulated commercial manufacturing environment.
• Strong collaborative skills to work seamlessly across cross-functional teams.
• An adaptable mindset - someone who thrives when timelines are moving fast but always remains accountable for deliverables.