Key Responsibilities:
- Design, develop, and maintain PLC programs, with a focus on Siemens platforms (S7, TIA Portal, WinCC, etc.).
- Troubleshoot, diagnose, and resolve PLC-related issues in the manufacturing process, minimizing downtime and optimizing equipment performance.
- Integrate and commission new equipment and systems into the existing manufacturing setup.
- Ensure all PLC-related operations comply with GMP and regulatory standards within the pharmaceutical industry.
- Perform regular system checks, updates, and backups to ensure the reliability and integrity of PLC systems.
- Collaborate with cross-functional teams, including maintenance, quality assurance, and process engineers, to improve operational efficiency.
- Document changes to software, hardware configurations, and processes as part of regulatory compliance.
- Train maintenance and production staff on PLC systems, troubleshooting, and safe operations.
Qualifications & Requirements:
- Bachelor's degree in Electrical Engineering, Automation, Mechatronics, or a related field.
- Atleast 5 years of hands-on experience with Siemens PLCs (S7, TIA Portal, WinCC) in a pharmaceutical or highly regulated industry.
- Solid understanding of GMP, cGMP, and regulatory compliance within the pharmaceutical sector.
- Strong knowledge of automation and control systems, including HMI/SCADA integration.
- Experience with validation protocols (IQ/OQ/PQ) is an advantage.
- Familiarity with industrial communication protocols such as Profibus, Profinet, and Ethernet/IP.
- Excellent troubleshooting and problem-solving skills.
- Ability to work both independently and as part of a team.
- Strong communication skills to collaborate effectively with internal teams and external vendors.
Preferred Skills:
- Experience with other PLC platforms is a plus.
- Knowledge of process control systems, instrumentation, and calibration in the pharmaceutical environment.
- Experience in continuous improvement methodologies such as Lean Manufacturing or Six Sigma.
