Automation & Vision for Regulated Manufacturing | Expert Insights from Verista

Life sciences manufacturers face constant pressure to improve quality, increase efficiency, and solve complex production challenges while maintaining compliance. In this edition of SME Insights & Perspectives, Chris Gilmet, Technical Subject Matter Expert at Verista specializing in engineering and automation, discusses how automation, vision systems, systems integration, and creative engineering can help regulated manufacturers solve difficult production and quality challenges. Topics discussed include: • Using automation to standardize manufacturing processes and quality • Improving process repeatability and confidence in regulated environments • Applying vision and automated inspection technologies to manufacturing challenges • Connecting equipment, data, rejection systems, reporting, and audit trails • Why systems integration is critical to successful inspection solutions • Identifying where AI can add meaningful value in manufacturing • Defining clear objectives, ROI, and validation guardrails for AI • Detecting hidden process variation through better testing and measurement • Developing custom automated test systems for complex medical devices • Applying multidisciplinary engineering expertise while maintaining compliance Whether you're responsible for Manufacturing Engineering, Automation, Quality, Validation, Vision Inspection, Systems Integration, Medical Device Manufacturing, Pharmaceutical Manufacturing, or Process Improvement, this discussion provides practical insight into solving complex regulated manufacturing challenges with the right combination of technology and engineering expertise. Learn more about Verista's engineering, automation, validation, and compliance services: https://verista.com/ Subscribe for additional SME Insights & Perspectives featuring Verista subject matter experts discussing today's most important life sciences challenges.