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Pharmaceutical Process/Cleaning Validation SME

2 weeks ago


Mumbai, Maharashtra, India Quascenta Full time ₹ 9,00,000 - ₹ 12,00,000 per year

IMPORTANT NOTE: Candidate should have prior work experience in Pharmaceutical Industry in QA role in Validation. Do NOT apply if you have software testing experience

Company Description

Quascenta specializes in offering comprehensive validation lifecycle management software solutions to empower pharmaceutical manufacturing sites. Our flagship products, e

Residue Pro, e

Process Pro, ValDoc Pro, QMS Pro and e

Log Pro, are designed to streamline QMS, product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. We provide innovative solutions tailored to meet unique requirements, with experienced Subject Matter Experts (SMEs) analyzing data and recommending improvements.

Role Description

This is a full-time on-site role. 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

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 using a QMS software
  • Experience in qualification of equipment/instruments
  • Experience in process validation a plus
  • Fluency in Hindi a must.