Manufacturing Execution System (MES) Engineer

Position: Assistant Manager Digital Manufacturing & Automation

Qualification: Bachelors degree in engineering Instrumentation/Computer Science, or related field.

Experience: 10 to 12 years in Biotech / Pharmaceutical

Key Responsibilities:

• Lead and manage both the MES team and the Automation team, ensuring efficient project execution and alignment with organizational goals.
• Drive PAS-X MES implementation projects across various phases including design, development, testing, and deployment and Maintenance.
• Oversee integration of PAS-X MES with shop floor equipment & ERP, ensuring seamless data exchange and operational efficiency.
• Manage Level 2 integration efforts with shop floor equipment, focusing on systems like GE iFix SCADA, Kepware OPC, Siemens PLC, and SCADA systems.
• Directly engage in PLC and SCADA programming, troubleshooting, and equipment maintenance activities.
• Maintain PAS-X MES recipes and recipe authoring processes in collaboration with relevant stakeholders.
• Provide technical leadership and guidance to team members, encourage a culture of continuous improvement and technical excellence.
• Collaborate with cross-functional teams including IT, engineering, operations, and quality assurance to ensure successful project outcomes.

Skill & Qualifications:

• Minimum of 6 years of experience in PAS|x MES implementation within the pharmaceutical industry and over all Min 10 years of experience in pharmaceutical Industry.
• Proven experience in integrating MES with shop floor equipment & ERP, particularly with Level 2 systems and SAP.
• Proficiency in GE iFix SCADA, Kepware OPC, Siemens PLC, and other relevant automation/ Historian technologies.
• Hands-on experience in PLC and SCADA programming, configuration, and troubleshooting.
• Strong understanding of equipment maintenance practices and methodologies.
• Experience in MES recipe authoring and managing recipe lifecycles.
• Strong analytical and problem-solving abilities, with a keen attention to detail.
• Familiarity with regulatory requirements and standards in the pharmaceutical industry (e.g., GMP, FDA regulations).