B Pharm/M.Pharm & Life Sciences Freshers Apply: QA Trainee Role at Immuneel Therapeutics, Bangalore

B Pharm/M.Pharm & Life Sciences Freshers Apply: QA Trainee Role at Immuneel Therapeutics, Bangalore

Apply for Quality Assurance Trainee role at Immuneel Therapeutics, Bangalore. Open for B Pharm, M.Pharm, BSc, MSc in Life Sciences. 0–2 years experience required.

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Quality Assurance Trainee Opportunity at Immuneel Therapeutics – Bangalore

For Freshers & Entry-Level Candidates with B Pharm, M.Pharm, BSc, MSc

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Join the Future of Personalized Cancer Therapy

Immuneel Therapeutics Pvt. Ltd., based in Bangalore, is revolutionizing cancer care through cutting-edge cell and gene therapy innovations. The company invites fresh graduates and early-career professionals to be part of their transformative journey by applying for the role of Trainee – Quality Assurance (Documentation Management System).

If you hold a degree in Pharmacy, Life Sciences, Biotechnology, Microbiology, or Chemistry and are passionate about quality compliance, this is your chance to start strong in the biopharma and healthcare sector.

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About Immuneel Therapeutics

Immuneel is India’s pioneering start-up in personalized immunotherapy, combining global science with a proudly Indian approach. With a vibrant, inclusive team and agile work culture, they aim to deliver high-quality engineered cell therapies to patients across the country.

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Role Overview: Trainee – Quality Assurance (Documentation Management System)

🧾 Department:

Quality Assurance

Reporting To:

Quality Assurance Lead

Duration:

6-month Traineeship
(On successful completion, may be considered for full-time role)

 Location:

Immuneel Therapeutics Pvt. Ltd.,
Mazumdar Shaw Medical Center, Narayana Health City,
Bommasandra Industrial Area, Bangalore – 560099

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Key Responsibilities

Document Control & Compliance

• Manage the lifecycle of GMP documents: creation, approval, issuance, archival, and disposal.

• Control issuance and traceability of BMRs, COAs, SOPs, and logbooks.

• Maintain document integrity using ALCOA+ principles.

 Change Management

• Support QMS activities like change controls, CAPAs, deviations, and audit readiness.

Periodic Review

• Monitor and update SOPs, manuals, and quality policies as per regulatory standards (Schedule-M, USFDA, EMA).

 Cross-Functional Coordination

• Work closely with QA, QC, R&D, and Manufacturing for documentation alignment and timely availability.

 Confidentiality & Security

• Ensure restricted access and confidentiality of sensitive documentation in compliance with internal SOPs.

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 Skills & Competencies

Technical

• Knowledge of GMP & GDP standards

• Hands-on experience in documentation systems

• Version control, document tracking, audit-readiness

 Soft Skills

• Detail-oriented and proactive

• Good communication and collaboration

• Time management and stress handling

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Required Qualifications

Experience Required:
0–2 years of experience in QA or document control in pharma/biotech industry. Exposure to cell and gene therapy is a plus.

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 Work Hours & Shift Details

• General Shift: 9:00 AM – 6:00 PM

• Post-Noon Shift: 2:00 PM – 11:00 PM (rotational)

• Weekly Off: 2 days (not necessarily weekends)

• Travel: Not Required

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How to Apply

 Send your updated resume to:
careers@immuneel.com

🔗 Or apply directly via LinkedIn:
👉 Click here to apply