Pharmaceutical Qualification SME

Role Overview: You will be working as a Pharmaceutical Validation SME at Quascenta, located in Chennai. Your main responsibility will be to provide technical support for software products such as ValDoc Pro, eLog Pro, and QMS Pro. This is a full-time on-site role where you will assist customers with managing qualification processes, executing qualification scripts, and writing test scripts. Key Responsibilities: - Provide technical support for software products including ValDoc Pro, eLog Pro, and QMS Pro - Assist customers with uploading SOPs and managing qualification processes - Execute qualification scripts such as IQ/OQ/PQ online - Write test scripts and open bug tickets as needed Qualifications Required: - BPharm or Biotechnology degree - Willingness to serve a minimum of 2 years with the company if offered a position Role Overview: You will be working as a Pharmaceutical Validation SME at Quascenta, located in Chennai. Your main responsibility will be to provide technical support for software products such as ValDoc Pro, eLog Pro, and QMS Pro. This is a full-time on-site role where you will assist customers with managing qualification processes, executing qualification scripts, and writing test scripts. Key Responsibilities: - Provide technical support for software products including ValDoc Pro, eLog Pro, and QMS Pro - Assist customers with uploading SOPs and managing qualification processes - Execute qualification scripts such as IQ/OQ/PQ online - Write test scripts and open bug tickets as needed Qualifications Required: - BPharm or Biotechnology degree - Willingness to serve a minimum of 2 years with the company if offered a position