Pharmaceutical quality management systems (PQMS) and validation lifecycle management are becoming increasingly digital across GMP-compliant manufacturing sites. If you are a BPharm graduate looking to build a career in pharmaceutical quality systems, validation software, and GMP compliance, this opportunity at Quascenta could be the right fit.
Quascenta is hiring a BPharm Graduate – PQMS Validation Software professional to support implementation and optimization of advanced validation lifecycle management software solutions for pharmaceutical manufacturing clients.
This role blends pharmaceutical manufacturing knowledge, PQMS expertise, data analysis, and regulatory compliance validation — making it ideal for pharmacy graduates interested in quality systems and digital transformation in pharma.
pharmaceutical manufacturing sites. Their core products include:
- eResiduePro – Residue calculation & cleaning validation software
- eProcessPro – Critical process parameter tracking
- eLogBook – Digital validation documentation management
With over 20 years of domain expertise, their tools are designed to ensure:
- GMP compliance
- Audit readiness
- Cost efficiency
- Operational process optimization
Job Overview
Position: BPharm Graduate – PQMS Validation Software
Location: Chennai, Tamil Nadu, India (On-site)
Employment Type: Full-Time
This pharmaceutical quality management systems (PQMS) role focuses on supporting software implementation, compliance validation, manufacturing data analysis, and regulatory documentation.
Key Responsibilities
The selected BPharm graduate will:
- Support implementation of PQMS validation software at pharma manufacturing sites
- Perform data analysis for manufacturing and cleaning validation processes
- Assist in GMP-compliant validation lifecycle management
- Customize software modules based on client-specific regulatory needs
- Track critical process parameters and residue calculations
- Prepare and support validation documentation for audits
- Provide client training and technical support
- Collaborate with cross-functional teams to enhance quality systems
This position combines pharmaceutical quality assurance knowledge with digital validation tools.
Required Qualifications
To qualify for this BPharm job in Chennai, candidates should have:
- Bachelor of Pharmacy (BPharm) degree
- Knowledge of Pharmaceutical Quality Management Systems (PQMS)
- Understanding of GMP-compliant manufacturing processes
- Familiarity with cleaning validation and residue calculation
- Exposure to validation lifecycle management
- Strong data analysis and documentation skills
- Effective communication for client training and audit support
- Ability to work independently in a structured environment
Academic excellence (Top 10% rank) will be considered an advantage.
Why This Role is Career-Enhancing for BPharm Graduates
This PQMS validation software job offers:
- Exposure to digital transformation in pharmaceutical manufacturing
- Hands-on experience in GMP compliance validation
- Direct involvement in regulatory documentation and audit readiness
- Skill development in validation lifecycle management
- Career path toward Quality Assurance, Validation, or Regulatory Systems
Professionals working in pharmaceutical validation software are increasingly in demand as manufacturing sites shift toward digital compliance platforms.
Salary (Estimated)
Based on industry benchmarks for entry-level validation and PQMS roles in Chennai:
₹3.0 – ₹4.5 LPA (CTC Estimated)
(Final offer may vary based on academic performance and technical expertise.)
