Quascenta Hiring BPharm Graduate – PQMS Validation Software | PQMS
- Quascenta Hiring BPharm Graduate – PQMS Validation Software | Pharma Quality Systems Career | Chennai
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Eligibility & Qualifications
- Educational Background
- Required Knowledge & Skills
- Location & Employment Details
- Application Process
- Frequently Asked Questions (FAQs)
- 1. Is this role open to fresh BPharm graduates?
- 2. Is prior manufacturing experience required?
- 3. What technical skills are important?
- 4. Will the role involve client interaction?
- 5. What long-term career benefits does this role offer?
- Summary Table
Quascenta Hiring BPharm Graduate – PQMS Validation Software | Pharma Quality Systems Career | Chennai
Quascenta is inviting applications for the position of BPharm Graduate – PQMS Validation Software in its pharmaceutical technology and validation solutions division. This is a full-time role based in Chennai, Tamil Nadu, designed for pharmacy graduates who want to build expertise in pharmaceutical quality management systems, validation lifecycle management, and GMP-compliant digital solutions for manufacturing sites. Fresh B.Pharm graduates are eligible to apply, and candidates with academic distinction or exposure to pharmaceutical manufacturing environments will have an added advantage.
This opportunity sits at the intersection of pharmaceutical manufacturing, regulatory compliance, and validation software implementation. It is ideal for candidates looking to move beyond traditional production or quality control roles and enter the high-growth area of digital quality systems and pharmaceutical compliance consulting.
Company Overview
entity[“organization”,”Quascenta”,”pharmaceutical validation software company”] specializes in advanced validation lifecycle management software solutions tailored for pharmaceutical manufacturing facilities. With over two decades of industry experience, the company focuses on digitizing and optimizing GMP-compliant processes across regulated environments.
Quascenta’s core products—eResiduePro, eProcessPro, and eLogBook—are engineered to simplify complex validation tasks such as residue calculation, critical process parameter tracking, cleaning validation documentation, and electronic record management. These platforms are designed to ensure regulatory compliance, operational efficiency, and cost optimization for pharmaceutical plants.
The organization builds its solutions on deep pharmaceutical domain knowledge, incorporating insights from industry experts in validation science and contamination control. By combining technical software development with pharmaceutical regulatory expertise, Quascenta supports global manufacturing sites in achieving inspection readiness, data integrity, and quality excellence.
Working with Quascenta means contributing to safer medicines and stronger compliance systems within the pharmaceutical industry.
Job Role & Responsibilities
The BPharm Graduate – PQMS Validation Software role focuses on supporting implementation, configuration, and optimization of pharmaceutical quality management software at manufacturing sites. The position requires both scientific understanding and technical adaptability.
Core Responsibilities
- Assist in implementing Pharmaceutical Product Quality Management Systems (PQMS) at client manufacturing sites.
- Support validation lifecycle activities including cleaning validation, residue calculations, and process parameter monitoring.
- Analyze manufacturing and cleaning data to ensure compliance with GMP standards.
- Customize software configurations based on client-specific validation and quality requirements.
- Maintain structured electronic documentation for audit readiness and regulatory inspections.
- Provide technical guidance and user training to quality assurance and manufacturing teams.
- Collaborate with cross-functional stakeholders to identify process optimization opportunities.
- Assist in preparing compliance documentation aligned with global regulatory expectations.
- Ensure data integrity principles are followed in digital quality systems.
This role requires attention to detail, analytical capability, and strong communication skills. The candidate will interact directly with pharmaceutical manufacturing professionals and quality assurance teams, making professional communication and regulatory understanding essential.
Eligibility & Qualifications
Educational Background
Bachelor’s degree in Pharmacy (B.Pharm) is mandatory.
Relevant educational qualifications include:
B.Pharm, M.Pharm (Quality Assurance, Pharmaceutics, Pharmaceutical Analysis), Pharm.D, MSc Pharmaceutical Chemistry, MSc Industrial Pharmacy, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, Clinical Research, Regulatory Affairs, or related life sciences disciplines.
Candidates graduating in the top 10% of their class will be given preference.
Required Knowledge & Skills
- Strong understanding of Pharmaceutical Quality Management Systems (PQMS).
- Knowledge of Good Manufacturing Practices (GMP) and regulatory compliance standards.
- Familiarity with validation lifecycle management concepts.
- Understanding of cleaning validation and residue calculation methodologies.
- Ability to interpret and analyze manufacturing process data.
- Strong documentation and technical writing skills.
- Excellent communication skills for client training and stakeholder interaction.
- Ability to work independently in a professional setting.
Prior exposure to pharmaceutical manufacturing operations, quality assurance departments, or validation activities will strengthen the candidate’s profile.
Location & Employment Details
- Location: Chennai, Tamil Nadu, India
- Employment Type: Full-Time
- Work Model: On-site / Client Coordination Based
Application Process
Interested candidates can apply directly through the official LinkedIn job listing using the link below:
Apply Here: https://www.linkedin.com/jobs/view/4372365397/
Applicants should highlight academic achievements, GMP knowledge, validation exposure, and any pharmaceutical manufacturing internship experience in their resumes.
Frequently Asked Questions (FAQs)
1. Is this role open to fresh BPharm graduates?
Yes. Fresh graduates with strong academic performance and GMP knowledge are encouraged to apply.
2. Is prior manufacturing experience required?
It is not mandatory but will be considered an advantage.
3. What technical skills are important?
Understanding of PQMS, validation lifecycle management, residue calculations, and data analysis is essential.
4. Will the role involve client interaction?
Yes. The candidate will provide training and technical support to pharmaceutical manufacturing clients.
5. What long-term career benefits does this role offer?
It opens pathways into validation consulting, quality systems leadership, and regulatory compliance roles within pharmaceutical organizations.
Summary Table
| Company | Quascenta |
| Vacancies | BPharm Graduate – PQMS Validation Software |
| Required Education | B.Pharm (mandatory), M.Pharm, Pharm.D, MSc Pharmaceutical Chemistry, Industrial Pharmacy, Biotechnology, Microbiology, Biochemistry, Clinical Research |
| Experience | Freshers eligible; pharmaceutical manufacturing exposure preferred |
To apply for this job please visit www.linkedin.com.
