PQMS Validation Software (B.Pharm)

Roles & Responsibilities:
• Support implementation of PQMS validation software at pharmaceutical manufacturing sites
• Perform data analysis for manufacturing and cleaning validation processes
• Assist in GMP-compliant validation lifecycle management
• Customize software modules to meet client-specific regulatory requirements
• Track critical process parameters and residue calculations
• Prepare and maintain validation documentation for audits
• Provide client training and technical support
• Collaborate with cross-functional teams to enhance quality systems

Qualification:
• 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 is preferred

Experience:
• Fresher or 0–2 years of experience in pharmaceutical quality systems or validation support

Skills:
• 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) is an advantage

About the Organization:
Quascenta is a technology solutions provider enabling digital transformation in pharmaceutical quality systems and validation lifecycle management. This role offers pharmacy graduates the opportunity to combine PQMS knowledge with advanced digital tools to enhance GMP compliance and quality operations.