Pharmaceutical Process Validation Support Associate

2 weeks ago


Kanpur, India Quascenta Full time

Company Description

Quascenta specializes in providing comprehensive validation lifecycle management software solutions for pharmaceutical manufacturing sites. With products like eResiduePro, eProcessPro, and eLog Pro, we aim to streamline product manufacturing and cleaning processes to ensure compliance, efficiency, and savings. Our solutions are designed by industry experts and tailored to meet the unique needs of each client, offering innovative and user-friendly tools for success.


Role Description

This is a full-time on-site role as a Process Validation Support Associate - PQMS at Quascenta's Chennai location. The role involves daily tasks such as providing technical support, assisting with demos to clients, and communicating effectively with team members and stakeholders. The Validation Support Associate will also be a part of the project team members working on new product development.


Qualifications

  • Prior experience in putting together APQR reports OR experience in Formulation & Development OR experience in process validation with PPQ runs and CPV runs. Note we are not looking for people with cleaning validation experience.
  • Fluency in Hindi a plus




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