Rajesh Kanna Email and Phone Number

 Ensure Process validation by establishing documented evidence which provides a high degree of assurance that a specific process will consistently produce a product meeting its pre-determined specifications and quality characteristics.  Managing written procedures for production and process control designed to assure that the products have the identity, strength, quality, and purity they purport or are represented to possess. Establish Control procedures to monitor the output and validate the performance of those manufacturing processes that may be responsible for causing variability in the characteristics of in-process material and the drug product. Initiate, implement, and control written manufacturing specifications and processing procedures to assure that the device conforms to its original design or any approved changes in that design. Strategic planning on Continuous improvement in Quality function apart from day to day activity.Materials Inspection - Incoming and In-House  Maintaining quality standards for incoming materials, ensuring stringent adherence to quality standards, norms & practices, identifying gaps and taking corrective action Responsible for in-house material testing of components.