Pharmaceutical Qualification SME

Role Overview: At Quascenta, you will be a Pharmaceutical Validation Subject Matter Expert (SME) based in Chennai, working full-time on-site. Your main responsibility will be to provide technical support on software products like ValDoc Pro, eLog Pro, and QMS Pro to companies in the pharmaceutical industry. You will play a crucial role in assisting customers with managing qualification processes and executing test scripts. Key Responsibilities: - Provide technical support on software products including ValDoc Pro, eLog Pro, and QMS Pro - Assist customers with uploading SOPs and managing qualification processes in the application - Execute qualification scripts (IQ/OQ/PQ) online for customers - Write and execute test scripts, and open bug tickets as needed Qualifications Required: - Bachelor's degree in Pharmacy (BPharm) or Biotechnology - Minimum commitment of 2 years with the company if offered the position,