Pharmaceutical Validation SME (Chennai)

Note: This position is based out of Chennai. No remote option available. Company DescriptionAt Quascenta, we specialize in offering comprehensive validation lifecycle management software solutions. Our mission is to empower pharmaceutical manufacturing sites with the software tools they need to streamline their product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. Our flagship products, including eResiduePro, eProcessPro, and eLogBook, are designed to revolutionize how companies manage their product, process, and cleaning lifecycles. With over 20 years of experience, our solutions support organizations in meeting regulatory requirements while optimizing operations.Role DescriptionThis is a full-time on-site role in Chennai or a Pharmaceutical Validation SME. The candidate will be responsible for providing technical support to companies on the following software products:ValDoc Pro - Qualification lifecycle management softwareeLog Pro - Electronic logbookQMS Pro - Quality Management system softwareYou will also be responsible for the following:Assist customers with uploading their SOPs and managing qualification in the application. Of interest to the customer will be the ability to execute qualification scripts (IQ/OQ/PQ) onlineWrite test scripts and execute them. Open bug tickets where required.QualificationsPrior experience using a QMS software, Validation roleExperience in qualification of equipment/instrumentsExperience in process validation a plus

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