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Projects Specialist Freshers Job at Quascenta Apply Now

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Projects Specialist job at Quascenta for BPharm and Biotech freshers. Check eligibility, salary, skills, and apply online today quickly.


Introduction

If you are a BPharm or Biotechnology graduate looking to begin your career in the pharmaceutical and digital quality domain, this opportunity can be a strong starting point. The Projects Specialist Job at Quascenta offers hands-on exposure to pharma software systems, validation processes, and compliance frameworks.

With the pharmaceutical industry rapidly shifting towards digital transformation, this role is ideal for freshers aiming to build expertise in pharma IT, quality systems, and validation.


Job Overview

DetailsInformation
Job TitleProjects Specialist (PQMS Software)
Company NameQuascenta
LocationChennai, Tamil Nadu, India
Employment TypeFull-time, On-site
DepartmentPharma Software / Quality Systems
Experience RequiredFreshers / Entry-Level
EducationBPharm / Biotechnology
Salaryβ‚Ή2.8 LPA – β‚Ή4.5 LPA

Company Overview

Quascenta is a growing organization focused on delivering innovative digital solutions for the pharmaceutical industry. The company specializes in pharmaceutical quality management systems (PQMS), helping manufacturers improve compliance, streamline processes, and ensure regulatory adherence through advanced software platforms.

Working here allows candidates to gain exposure to cutting-edge pharma technologies and global compliance standards.


Job Location & Employment Type

  • Location: Chennai, Tamil Nadu
  • Job Type: Full-time, On-site
  • Candidates must be willing to work from the office and collaborate with cross-functional teams.

Open Positions / Department Details

  • Role: Projects Specialist (PQMS Software)
  • Department: Pharmaceutical Software & Validation Systems
  • Focus area includes quality management systems, validation lifecycle, and software testing within pharma environments.

Key Roles & Responsibilities

As a Projects Specialist, your responsibilities will include:

  • Executing test cases for PQMS software applications
  • Performing software validation in compliance with pharma standards
  • Identifying bugs or defects and supporting quality assurance processes
  • Assisting in implementation of digital quality tools
  • Providing training and guidance to clients on software usage
  • Supporting continuous improvement initiatives
  • Collaborating with pharma manufacturing teams for system enhancement
  • Ensuring documentation and compliance with regulatory requirements
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Eligibility Criteria

Education

  • Bachelor’s degree in:
    • BPharm
    • Biotechnology

Experience

  • Freshers can apply
  • Entry-level candidates with basic pharma knowledge preferred

Skills Required

  • Strong analytical and problem-solving ability
  • Basic understanding of pharmaceutical manufacturing processes
  • Good communication skills for client interaction
  • Attention to detail in testing and validation
  • Ability to work independently and manage tasks efficiently

Preferred Skills (Good to Have)

  • Knowledge of Computer System Validation (CSV)
  • Understanding of GxP guidelines
  • Exposure to QA/QC processes in pharma
  • Interest in pharma IT, SaaS, or digital systems
  • Basic knowledge of validation lifecycle

Salary & Benefits

  • Salary Range: β‚Ή2.8 LPA – β‚Ή4.5 LPA
  • Exposure to pharma software platforms
  • Opportunity to work on validation and compliance systems
  • Career growth in QA, validation, and pharma IT
  • Experience with global regulatory standards
  • Skill development in digital pharma technologies

Selection Process

The selection process typically includes:

  1. Application screening
  2. Technical or aptitude assessment
  3. Interview (HR + Technical)
  4. Final selection

How to Apply

  • Candidates need to apply through the online application link provided by the company.
  • Ensure your resume is updated with relevant academic and technical details before applying.

Important Dates

  • Last date to apply: Not specified (Apply as early as possible)

Why Apply for This Job?

This Projects Specialist Job at Quascenta is a valuable opportunity for freshers who want to enter the pharmaceutical industry through a modern, technology-driven pathway.

Here’s why this role stands out:

  • Strong entry into pharma IT and validation domain
  • High demand career path in digital quality systems
  • Exposure to real-time software implementation projects
  • Opportunity to build expertise in compliance and QA systems
  • Ideal foundation for careers in:
    • Pharma validation
    • Regulatory affairs
    • Clinical data systems
    • Quality assurance
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FAQs

1. Who can apply for this job?

Candidates with a BPharm or Biotechnology degree are eligible to apply.

2. What is the salary range for this role?

The expected salary ranges between β‚Ή2.8 LPA and β‚Ή4.5 LPA.

3. Is prior experience required?

No, this role is open for freshers and entry-level candidates.

4. How can I apply?

You can apply through the official online application link provided by the company.

5. What skills are important for this job?

Analytical thinking, communication skills, attention to detail, and basic pharma knowledge are essential.


Conclusion

The Projects Specialist Job at Quascenta is an excellent opportunity for fresh graduates to step into the evolving world of pharmaceutical technology and quality systems. With the increasing adoption of digital tools in pharma, this role offers long-term career growth and industry-relevant experience.

If you are interested in pharma IT, validation, and compliance, this job can be the perfect starting pointβ€”apply as soon as possible.


Disclaimer

PharmaJobHub.in is an independent job information platform. We do not provide jobs or recruitment and are not affiliated with any company.


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