Computer System Validation Engineer

As a Computer System Validation Engineer at our company, you will play a crucial role in the Quality Assurance/Validation department in Hyderabad. With 4-5 years of experience, you will be responsible for preparing, executing, and compiling qualification documents for pharmaceutical manufacturing equipment, specifically Fluid Bed Processors (FBP), Rapid Mixer Granulators (RMG), Compression machines, and Coating machines. Your key responsibilities will include preparing, executing, and compiling qualification protocols and reports for pharmaceutical equipment, conducting Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for the mentioned machines, ensuring compliance with regulatory standards and company policies, collaborating with cross-functional teams, maintaining accurate documentation, and identifying and resolving issues related to qualification processes promptly. To excel in this role, you should possess 4-5 years of hands-on experience in qualification documentation preparation, execution, and compilation, technical expertise in the qualification and validation of FBP, RMG, Compression, and Coating machines, a strong understanding of Good Manufacturing Practices (GMP) and regulatory guidelines, excellent documentation and communication skills, and the ability to work effectively in a team environment. If you are passionate about validation and qualification activities and are looking to contribute your expertise to a dynamic team, we encourage you to apply for this Full-Time position.,