Looking to start your career in the pharmaceutical industry with a focus on quality systems and software? A promising opportunity is now open at Quascenta for the role of Projects Specialist (PQMS Software) in Chennai. This position is ideal for BPharm and Biotechnology graduates aiming to build expertise in pharmaceutical product quality management systems (PQMS), validation, and software quality assurance.
With increasing demand for digital transformation in pharma manufacturing, roles like this are highly valuable for candidates interested in pharma IT, validation lifecycle, and compliance systems.
Job Overview
- Company: Quascenta
- Role: Projects Specialist (PQMS Software)
- Location: Chennai, Tamil Nadu, India
- Job Type: Full-time, On-site
- Experience: Freshers / Entry-level
- Industry: Pharmaceutical Software / Validation Systems
Key Responsibilities
- Execute test cases and ensure software quality for PQMS platforms
- Perform software validation and testing aligned with pharma compliance standards
- Identify defects and support quality assurance processes
- Assist in implementation of PQMS solutions like eResiduePro, eProcessPro, and eLogBook
- Provide client training and support on software usage
- Contribute to process improvement and analytical problem-solving
- Work closely with pharma manufacturing teams for system optimization
Required Qualifications
- Bachelorโs degree in BPharm or Biotechnology
- Strong understanding of pharmaceutical manufacturing processes (preferred)
- Good analytical and problem-solving skills
- Strong communication skills for client interaction and training
- Ability to work independently and manage responsibilities
- High attention to detail in software testing and validation
Preferred Skills (Good to Have)
- Knowledge of CSV (Computer System Validation)
- Familiarity with GxP guidelines and regulatory compliance
- Exposure to pharma QA/QC or validation processes
- Interest in pharma IT, SaaS, or digital quality systems
Salary & Benefits (Estimated)
- Salary Range: โน2.8 LPA โ โน4.5 LPA
- Opportunity to work on cutting-edge pharma software platforms
- Exposure to global regulatory standards
- Career growth in pharma validation, QA, and digital systems
- Hands-on experience with industry-leading PQMS tools
Why This Role Matters
The pharmaceutical industry is rapidly adopting digital quality management systems, creating demand for professionals skilled in PQMS, validation, and software QA. This role provides a strong foundation for careers in:
- Pharmacovigilance (PV systems exposure)
- Clinical data & validation roles
- Regulatory compliance & QA
- Pharma SaaS and IT systems
How to Apply
