Website:
tulsitherapeutics.com
Job details:
About Tulsi Therapeutics:
A pioneering biotechnology venture dedicated to advancing regenerative cellular therapies through rigorous research, precision manufacturing, and global distribution of next-generation stem cell and exosome-based treatments. Our mission is to address some of the world’s most challenging and life-threatening medical conditions—particularly those with limited or ineffective therapeutic options—by
delivering innovative solutions that restore hope and improve patient outcomes. We aim to develop a “Made in India” therapeutic solution that is globally competitive in quality and affordability, positioning India as a hub for advanced cell therapy solutions.
Our Vision
We are committed to Democratizing Stem Cell Therapy by transcending socio- economic barriers and bringing hope and effective treatment options to patients worldwide.
Our Mission
We strive for Excellence in Manufacturing for Maximum Clinical Impact, ensuring the highest quality and ethical production of stem cells and exosomes, thereby setting new benchmarks in regenerative medicine.
Job Purpose
To perform and support GMP microbiology activities for a cell therapy manufacturing facility, ensuring effective microbiological control of manufacturing areas, utilities, materials and products in compliance with applicable GMP requirements.
Key Responsibilities
- Perform Environmental Monitoring (EM) including active air, settle plates, surface monitoring and personnel monitoring.
- Perform sterility testing of raw materials, process samples and finished cell therapy products.
- Perform microbiological testing of purified/process water and support water-system monitoring.
- Perform Bacterial Endotoxin Testing (BET) including PPC, inhibition/enhancement and method suitability.
- Perform Mycoplasma testing, preferably using PCR/qPCR-based methods.
- Perform Growth Promotion Testing (GPT), media sterility checks and microbiological media management.
- Support EM, water and microbiological trend analysis and periodic reporting.
- Support OOS/OOT, deviation, excursion, investigation and CAPA activities.
Qualification: M.Sc.in Microbiology, Biotechnology, Life Sciences or equivalent
Experience: 4–6 Years of hands-on QC Microbiology experience in a GMP environment.
Industry Preference: Stem Cell / Cell Therapy / Biologics / Sterile & Parenteral GMP
Interested in this opportunity? Kindly send your resume to mahesh.c@tulsitherapeutics.com
Click on Apply to know more.
