PHARMA BHARAT
PHARMACEUTICAL JOB PORTAL
No new notifications

Advertisement

BPharm Freshers QA PQMS Validation Software Job in Quascenta

Published on

If youโ€™re a BPharm graduate looking to enter the world of pharmaceutical quality management systems (PQMS) and validation lifecycle software, this opportunity at Quascenta, Chennai is one of the best roles to build a high-growth career.

Quascenta is known for its advanced validation lifecycle management toolsโ€”eResiduePro, eProcessPro, and eLogBookโ€”used across leading pharmaceutical manufacturing companies. This role offers hands-on exposure to GMP compliance, software validation, data analysis, and regulatory documentation, making it ideal for freshers and early-career pharma professionals.

Advertisement

๐Ÿ” Role Overview

As a BPharm Graduate โ€“ PQMS Validation Software Specialist, youโ€™ll support clients in implementing Quascentaโ€™s validation software, ensuring compliance, accuracy, and audit readiness across pharma manufacturing processes.


๐Ÿงช Key Responsibilities

  • Support the implementation of PQMS and validation lifecycle management software
  • Perform data analysis for cleaning validation, residue calculations & critical parameters
  • Document GMP-compliant validation processes
  • Customize software workflows based on client manufacturing processes
  • Provide remote training and technical support to users
  • Assist in regulatory audits and documentation
  • Collaborate with quality, production, and IT teams for process optimization
  • Ensure adherence to GMP, GxP, and regulatory standards

๐ŸŽ“ Required Qualifications

  • B.Pharm degree (mandatory)
  • Strong understanding of PQMS, GMP, and pharma quality systems
  • Knowledge of validation lifecycle management
  • Ability to evaluate manufacturing and cleaning process data
  • Proficiency in documentation and compliance activities
  • Excellent communication skills for client training
  • Ability to work independently in a remote/onsite hybrid model
  • Experience in pharma manufacturing (preferred but not mandatory)

โœจ Benefits

  • Exposure to real-world validation & compliance projects
  • Work with industry-leading pharma software
  • Skill development in GMP, validation, and digital QMS tools
  • Opportunity to work closely with global pharma experts
  • Competitive salary and growth-focused environment
  • Remote collaboration with cross-functional teams

๐Ÿ“ Job Location

Chennai, Tamil Nadu, India (On-site)


๐Ÿ’ฐ Salary Range (Industry Standard Estimate)

INR 3.0 โ€“ 5.0 LPA
(Final CTC may vary based on skills & experience)


๐Ÿ“ How to Apply

Application Link

Share This Job

โœ… Job Details Copied!