MANUFACTURING ASSOCIATE/SPECIALIST– STEM CELL THERAPY Location: Bengaluru, India

Biopatrika; Bengaluru; On-site; INR 900,000 - 1,400,000; Full time

Job summary

EyeStem in Bengaluru is seeking a Manufacturing Associate/Specialist for stem cell therapy products. The role requires 4–5 years of GLP/GMP/GxP experience with MSc/MTech in Life Sciences or related fields, and hands-on cell culture expertise.

You will execute GMP-compliant manufacturing, document per SOPs, and collaborate across QA, QC, Process Development, and Regulatory teams to ensure data integrity and readiness of facilities and equipment.

Qualifications

• M.Sc. or M.Tech in Life Sciences or related field.
• 4–5 years of experience in GLP, GMP, or GxP-regulated environments.
• Hands-on mammalian or stem cell culture experience.
• Strong attention to detail and data integrity.
• Ability to work in a fast-paced, cross-functional team.

Responsibilities

• Execute GMP-compliant manufacturing activities for stem cell products.
• Perform and document manufacturing activities per SOPs, batch records, and GMP.
• Support cell culture, expansion, harvesting, formulation, cryopreservation.
• Ensure aseptic processing and contamination control in sterile environments.
• Support process optimization, scale-up, tech transfer, and investigations.
• Collaborate with QA, QC, Process Development, Engineering, and Regulatory teams.
• Maintain accurate and compliant documentation with GxP and data integrity.
• Assist facility, equipment, and manufacturing readiness activities.

Skills

GMP Compliance

Cell Culture

GMP Documentation

Data Integrity

Cross-functional

Education

M.Sc./M.Tech in Life Sciences

Tools

Sterile Manufacturing

Job description

# MANUFACTURING ASSOCIATE/SPECIALIST– STEM CELL THERAPY Location: Bengaluru, IndiaJobBangalore, IndiaOctober 5, 2026Full Time### Job Overview* Date Posted October 5, 2026* Location Bangalore, India* Expiration date November 4, 2026* Click to apply: https://www.linkedin.com/posts/were-hiring-manufacturing-associatespecialist-share-7512769300559241216-oMlh/### Job DescriptionWE’RE HIRING | MANUFACTURING ASSOCIATE/SPECIALIST– STEM CELL THERAPY Location: Bengaluru, India Experience: 4–5 years Qualification: M.Sc. / M.Tech. or equivalent Application Deadline :20 October 2026 Key Responsibilities • Execute GMP-compliant manufacturing activities for stem cell/iPSC-derived cell therapy products. • Perform and document manufacturing activities in accordance with approved SOPs, batch manufacturing records, and GMP requirements. • Support cell culture, differentiation, expansion, harvesting, formulation, cryopreservation, and related manufacturing processes. • Ensure adherence to aseptic processing and contamination control practices in a sterile manufacturing environment. • Support process optimization, scale-up, process characterization, and technology transfer activities. • Participate in manufacturing investigations, deviations, CAPA, change controls, and continuous improvement initiatives. • Collaborate closely with QA, QC, Process Development, Engineering, and Regulatory teams. • Maintain accurate and compliant documentation in accordance with GxP and data integrity requirements. • Support facility, equipment, and manufacturing readiness activities as required.What We’re Looking For • 4–5 years of relevant experience in GLP, GMP, or GxP-regulated environments, preferably within sterile manufacturing, cell therapy, or advanced therapy medicinal products (ATMPs). • M.Sc., M.Tech., or equivalent qualification in Life Sciences, Biotechnology, Microbiology, Biochemistry, or a related discipline. • Hands-on experience in mammalian cell culture and/or stem cell culture. • Good understanding of aseptic processing, GMP documentation, and controlled manufacturing environments. • Strong attention to detail and commitment to quality and data integrity. • Ability to work effectively in a cross-functional, fast-paced environment. Added Advantage Experience in cell and gene therapy / ATMP manufacturing or product testing, along with familiarity with regulatory expectations for biologics and cell therapy products, will be highly valuable. Interested candidates: Please send your CV to [e-mail]