Pharmaceutical Process/Cleaning Validation SME

IMPORTANT NOTE: Candidate should have prior work experience in Pharmaceutical Industry in QA role in Validation. Do NOT apply if you have software testing experience Company Description Quascenta specializes in offering comprehensive validation lifecycle management software solutions to empower pharmaceutical manufacturing sites. Our flagship products, eResidue Pro, eProcess Pro, ValDoc Pro, QMS Pro and eLog Pro, are designed to streamline QMS, product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. We provide innovative solutions tailored to meet unique requirements, with experienced Subject Matter Experts (SMEs) analyzing data and recommending improvements. Role Description This is a full-time on-site role. The candidate will be responsible for providing technical support to companies on the following software products: ValDoc Pro - Qualification lifecycle management software eLog Pro - Electronic logbook QMS Pro - Quality Management system software You 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) online Write test scripts and execute them. Open bug tickets where required. Qualifications Prior experience using a QMS software Experience in qualification of equipment/instruments Experience in process validation a plus Fluency in Hindi a must. Show more Show less