Pharmaceutical Qualification SME

The position is based out of Chennai and does not offer a remote work option. The salary offered is between 5-8 lacs CTC based on validation experience. At Quascenta, we specialize in providing comprehensive validation lifecycle management software solutions. Our mission is to empower pharmaceutical manufacturing sites by offering software tools to streamline product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. Our flagship products, such as eResiduePro, eProcessPro, and eLogBook, aim to transform how companies manage their product, process, and cleaning lifecycles. With over 20 years of experience, our solutions help organizations meet regulatory requirements while enhancing operations. This full-time on-site role is for a Pharmaceutical Validation Subject Matter Expert (SME) based in Chennai. The selected candidate will offer technical support on software products like ValDoc Pro, eLog Pro, and QMS Pro to client companies. Responsibilities include assisting customers with uploading SOPs, managing qualifications in the application, executing qualification scripts (IQ/OQ/PQ) online, writing and executing test scripts, and opening bug tickets when necessary. Qualifications for the role include prior experience with QMS software, equipment/instrument qualification, and process validation. Fluency in Hindi is a mandatory requirement.,