Manufacturing Executive

CAR-T Cell Therapy Manufacturing Executive

Micro CRISPR is a leading biotechnology company dedicated to revolutionizing cancer treatment through advanced cell and gene therapy solutions. Our mission is to develop cutting-edge immunotherapies that transform patient outcomes. We are seeking a highly skilled and experienced CAR-T Cell Therapy Manufacturing Executives to work in our manufacturing operations and ensure the efficient production of high-quality cell therapy products.

Role

Summary:

The CAR-T Cell Therapy Manufacturing Executives will work for the end-to-end manufacturing processes for CAR-T cell therapy manufacturing, ensuring compliance with Good Manufacturing Practices (GMP) and regulatory requirements. This role requires strong knowledge of concepts of cell culture, operational expertise, and a deep understanding of cell therapy manufacturing.

Key Responsibilities:

- Execution of the CAR-T cell therapy manufacturing process as per schedule

- May have to work in shift and as per process
- Monitoring and reviewing the qualification of equipment in cGMP facility.
- Preparation and review of EOPs, SOPs and BMRs related to manufacturing process.
- Preparation and review of EOPs, SOPs related to manufacturing facility.
- Reporting the breakdown of any equipment in the manufacturing facility.
- Manufacturing of CAR-T cells in cGMP environment and preparation of related documents as per quality compliance.
- Coordination with QC for sharing of In-process and final product samples and preparation of associated documents.
- Coordination with warehouse department for storage and issuance of raw material and finished product.
- Coordination with QA department for timely completion of manufacturing related documents as per quality policy.
- Actively contribute in the inventory management and procurement of reagent and consumables required for manufacturing.
- Analyse the data and prepare the presentations of batch manufacturing.
- Participate in the process development activities of CAR-T manufacturing process. Analyse data and prepare the reports and maintain related documents.
- Timely completion of the documents related to cGMP manufacturing as per QA compliance.
- Review the literature and participate in scientific discussions and presentations.

Requirement of skills:

- Minimum of 1-2 years of industrial experience. Fresher’s can also apply.
- Proficiency in handling animal cell culture in biosafety cabinets. Candidates handled animal cell lines will be preferred
- Preparation of media and buffers for animal cell culture
- Concepts should be clear with respect to Immunology, cell culture, cancer, transformed and primary cell lines, etc
- Basic understanding related to buffer preparation, cryopreservation and thawing of cells
- Should have handled Biosafety cabinets, centrifuge, inverted microscope, cell counter, cell count by trypan blue staining, aseptic handling procedures, etc
- Concepts related to genetic modification by transfection, transformation, and transduction should be clear.
- Consepts related to genes, proteins, transcription, translation should be clear

Educational qualification:

Master degree in Biotechnology, Microbiology, Pharamceutics, etc