(5-10 yr experience ) Pharmaceutical Qualification SME

Note : This position is based out of Chennai. No remote option available.

Company Description

At 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 Description

This is a full-time on-site role for a Pharmaceutical Validation SME located in Chennai. 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

eProcess Pro - Process Validation

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 in Process Validation with PPQ Runs

Experience in qualification of equipment / instruments

Fluency in Hindi a must.