NIMHANS Genetics & Biochem Project Job Opening, Applications Invited
NIMHANS Genetics & Biochem Project Job Opening, Applications Invited. MSc genetics, human genetics, applied genetics, medical genetics, human disease genetics, biochemistry candidates can apply for a project job at NIMHANS. Senior Project Associate at NIMHANS. Interested candidates can check the details below and apply.
Possible Interview Questions are posted below
This job expires in
NIMHANS/DBT/NOTI/GKC/SPA/2023-24
NOTIFICATION
Applications are invited from eligible candidates for the post of “Senior Project Associate” on contract basis in the R&D project entitled “Mission Program on Pediatric Rare Genetic Disorders” funded by Department of Biotechnology (DBT) under Dr. Chetan GK, Professor and Head of Human Genetics, NIMHANS.
Name of the Post: Senior Project Associate
No. of Posts: 01
Name of the Project: “Mission Program on Pediatric Rare Genetic Disorders”
Name of the PI: Dr. Chetan GK
Maximum Age Limit: 40 Years
Duration of project : 5 years. Initial appointment will be made for the period of 6 months, with extension up to the term of the project after revaluation
Selection process: Written Examination and Personal interview
How to Apply: Eligible candidates fulfilling the criteria may apply through the given link above. The last
date for receipt of the applications is within 14 days of this notification and applications received after the last date will not be considered.Essential Qualification:
- Master’s degree biomedical sciences, preferably genetics, human genetics, applied genetics, medical genetics, human disease genetics, biochemistry or related areas from a recognized University or Institution
AND - (i) Minimum three to four years’ experience in Research and Development in Industrial and Academic Institutions or Science and Technology Organizations and Scientific activities and services
OR - (ii) Doctoral Degree in Science/Engineering/Technology/Pharma /MD/MS from a recognized University or equivalent
Desirable Experience: Experience in genomics, Next-Generation Sequencing (NGS) (wet lab and/or bioinformatics) focused on Human Genetics and clinical applications.
Nature of the work: Handling of biological samples, cataloging, isolation of nucleic acids, QC, NGS library preparation and sequencing, bioinformatic analysis, variant interpretation & reporting.
Salary: Rs. 42,000/- + 24% HRA
Check the notification below
Possible Interview Questions:
- Can you describe your experience and expertise in the field of pediatric rare genetic disorders and related research?
- My experience in the field of pediatric rare genetic disorders includes working on research projects focused on identifying and understanding these disorders. I have a Master’s degree in biomedical sciences, with a specialization in genetics, and have gained hands-on experience in handling biological samples, performing nucleic acid isolation, conducting Next-Generation Sequencing (NGS) experiments, and analyzing genomic data for variant interpretation and reporting.
- How have you applied your research and development experience in industrial and academic institutions or science and technology organizations to advance the field of human genetics?
- During my previous roles in research and development, I have actively contributed to advancing the field of human genetics. I have collaborated with multidisciplinary teams to design and execute experiments, develop protocols for genomic analyses, and contribute to the interpretation of genetic data. Additionally, I have engaged in scientific activities and services that have supported the understanding and management of genetic disorders.
- Can you explain your familiarity with genomics and Next-Generation Sequencing (NGS) techniques, both in wet lab and bioinformatics aspects, for human genetics and clinical applications?
- I have hands-on experience in both wet lab and bioinformatics aspects of genomics and Next-Generation Sequencing (NGS) techniques. In wet lab work, I have performed library preparation and sequencing using NGS platforms, ensuring high-quality results. In bioinformatics, I have analyzed NGS data, performed variant calling, annotation, and prioritization, and utilized relevant databases and tools for genomic interpretation and reporting.
- How would you approach the handling of biological samples, cataloging, isolation of nucleic acids, quality control, and NGS library preparation for the research project on pediatric rare genetic disorders?
- For the research project on pediatric rare genetic disorders, I would adhere to standardized protocols and best practices for handling biological samples. I would ensure accurate cataloging and labeling of samples, implement efficient techniques for nucleic acid isolation, and perform rigorous quality control checks to maintain data integrity. Additionally, I would follow established procedures for NGS library preparation, ensuring optimal library quality and sequencing efficiency.
- How do you stay updated with the latest advancements and developments in the field of pediatric rare genetic disorders and genomics?
- To stay updated with the latest advancements and developments in the field, I regularly engage in continuous learning and professional development activities. I actively participate in scientific conferences, workshops, and seminars focused on pediatric rare genetic disorders and genomics. I also subscribe to relevant scientific journals and follow reputable online resources and research publications. This allows me to stay informed about emerging technologies, novel research findings, and advancements in the field, enabling me to contribute effectively to the research project.
These sample answers provide a starting point and can be tailored based on the candidate’s specific experiences and achievements.
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