Develop, configure, and optimize PLC programs for automated equipment used in sterile injectable manufacturing.
Design and implement control systems (SCADA, DCS, HMI) ensuring compliance with pharma-grade standards.
Collaborate with cross-functional teams to resolve automation-related issues.
Provide technical guidance and training to operators and maintenance staff.
Manage vendor relationships for automation hardware/software procurement and integration.
Ensure projects are delivered on time, within budget, and aligned with regulatory and safety standards.
Prepare and maintain documentation including URS (User Requirement Specifications), FRS (Functional Requirement Specifications), Design Qualification (DQ), and Validation protocols.
Ensure compliance and other regulatory guidelines for automation systems.
Maintain audit-ready records for system changes, upgrades, and validations.
Lead Factory Acceptance Testing (FAT)



and Site Acceptance Testing (SAT) for automation systems.
Oversee commissioning, qualification, and validation of PLC-controlled equipment.
Ensure robust change control and risk assessment during system modifications.
Identify prospects for automation upgrades to improve efficiency, reliability, and compliance.
Implement Industry 4.0 concepts such as IoT, predictive maintenance, and data analytics.
Drive initiatives for digital transformation in manufacturing operations.
Core Competency:

-Advanced PLC/SCADA system knowledge
-GMP & validation expertise
-Change control & compliance management
-Automation project leadership
-Vendor management
-Strategic automation planning
-Team leadership
-Risk assessment capability

📌 Plc Programming Manager Ahmedabad
🏢 Otsuka Pharmaceutical
📍 Ahmedabad