Engage with users to gather, analyze, and document business requirements related to manufacturing processes.
Oversee the delivery of large, global projects, ensuring adherence to timelines, budgets, and quality standards.
Lead the complete life cycle implementation of Manufacturing Execution Systems (MES) using a COTS product (e.g., Camstar Enterprise Platform or GE Proficy).
Define and implement the Factory Model, ensuring alignment with business goals and compliance requirements.
Apply in-depth knowledge of medical devices and pharmaceutical manufacturing processes to inform project decisions and solutions.
Collaborate with teams to ensure seamless integration between MES and external applications (e.g., ERP, LIMS, equipment, HMI).
Ensure compliance with computer system and manufacturing validation processes, facilitating necessary documentation and testing.
Utilize SQL for data extraction and reporting, contributing to informed decision-making and system optimization.
Required Technical/Functional Skills
Proven experience in manufacturing processes, particularly in medical devices and pharmaceuticals.
Track record of managing and delivering large-scale, global projects with a focus on quality and stakeholder satisfaction.
Hands-on experience with MES implementation, particularly with products like Camstar or GE Proficy.
Familiarity with interfacing MES applications with ERP systems, LIMS, and other manufacturing equipment.
Understanding of validation processes related to computer systems and manufacturing environments.
Competency in SQL for querying databases and generating reports.