Immuneel Therapeutics Hiring QA Trainee | Pharma Jobs

Follow Us  
Image: Immuneel Therapeutics Hiring QA Trainee | Pharma Jobs

Immuneel Therapeutics Pvt. Ltd., a pioneering start-up in the field of personalized immunotherapy, is inviting applications for the role of Trainee – Quality Assurance (Documentation Management System) at its Bangalore location. This opportunity is ideal for fresh graduates or early-career professionals passionate about GMP documentation and quality compliance.

Job Overview

Job Role: Trainee – Quality Assurance (DMS) | Location: Bangalore, Karnataka | Experience: 0–2 Years | Application Mode: Email/LinkedIn

Job Details

Organization: Immuneel Therapeutics Pvt. Ltd.
Position: Trainee – Quality Assurance (Documentation Management System)
Qualification: B.Pharm, M.Pharm, BSc, MSc in Biotechnology, Microbiology, Biochemistry, or Chemistry
Location: Mazumdar Shaw Medical Center, Narayana Health City, Bommasandra Industrial Area, Bangalore – 560099
Posted On: April 13, 2025
Work Hours: 9:00 AM – 6:00 PM / 2:00 PM – 11:00 PM (rotational)
Shift & Off: 2 Weekly Offs (not fixed on weekends)
Experience Required: 0–2 years in QA/document control in pharma/biotech. Cell and gene therapy experience is a plus.

About Immuneel Therapeutics

Immuneel is India’s first dedicated personalized immunotherapy company, focused on bringing cutting-edge cell and gene therapy solutions to cancer care. Founded with a global mindset and Indian heart, Immuneel offers a collaborative and mission-driven culture for aspiring professionals in the biotech space.

Key Responsibilities

  • Document Control & Compliance: Manage GMP documentation lifecycle – creation, approval, issuance, archival, and disposal.
  • Issue and track documents such as BMRs, COAs, SOPs, and logbooks.
  • Ensure compliance using ALCOA+ principles.
  • Change Management: Assist in managing change controls, CAPAs, deviations, and audit-readiness activities.
  • Periodic Review: Ensure timely review and update of SOPs and manuals in line with global and Indian regulatory guidelines.
  • Cross-Functional Coordination: Work closely with QA, QC, R&D, and Manufacturing teams for documentation accuracy and availability.
  • Confidentiality & Security: Handle sensitive documents per SOPs with strict confidentiality.

Skills & Competencies

  • Technical: Knowledge of GMP and GDP standards; familiar with document versioning and audit-readiness.
  • Soft Skills: Detail-oriented, good communicator, collaborative, and able to manage time effectively under pressure.

Qualifications

  • Minimum: B.Pharm, M.Pharm, BSc or MSc in Biotechnology, Microbiology, Biochemistry, or Chemistry.
  • Experience: 0–2 years in QA/documentation. Exposure to biopharma or cell/gene therapy will be an advantage.

Why Join Immuneel?

  • Hands-On Learning: Practical experience in a fast-evolving immunotherapy environment.
  • Innovative Culture: Work with a motivated and collaborative team solving real-world oncology problems.
  • Career Advancement: Potential for full-time opportunity upon successful traineeship completion.

How to Apply

Send your updated CV to: [email protected]

Or apply directly via Link below:

Apply Now
Join our  Whatsapp Channel/Group  for Receive Latest job updates, join us on Telegram for further information and all updates.
Drx SohanLal Kushwaha Updated - April 15, 2025 By Drx SohanLal Kushwaha
#B.Pharm #BSc

Write Your Comment

Web Stories Show All

Most applied jobs

ads go here