Master Degree in Biotechnology, Biochemistry from a recognized university. Research / working experience in regulatory framework, and having the experience of handling small laboratory animals, etc. Analysis of Micro- Nanoplastics in food matrices; Micro and Nanoplastics as emerging food contaminants : Establishing validated methodologies and understanding the prevalence in different food matrices
Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India. The company manufactures generic pharmaceuticals and active pharmaceutical ingredients.
Post Graduate degree in Life Science, Pharmacy, including the integrated PG degrees. Candidate with a Ph. D degree with specialization in Pharmaceutics, Pharmacology and Toxicology, Biotechnology, Life Sciences, Pharmacy and or significant experience in the formulation and development of nanotechnology-based drug delivery systems, clinical research, In vitro and In vivo models and molecular biology.
Bachelor of Pharmacy B.Pharma degree with at least 02 years of experience in AYUSH Hospitals, Clinics. In case B.Pharma candidate is not available, Diploma in Pharmacy D.Pharma candidates with at least 02 years of experience will be considered. Should have computer knowledge.
The Engagement shall be made through a process of Walk in Interview against Academic performance Index- 100 marks and Interview - 10 marks- Moreover, 5 marks wilt be given to the Degree holder in pharmacy, in addition.
The candidate will be responsible for performing a range of wet-lab based analyses, which include routine semen analysis, sperm DNA Fragmentation Index assessment, Y-chromosome microdeletion testing, RNA extraction, DNA extraction, protein extraction, PCR analysis, and ELISA assays. These tasks will be carried out as part of the broader study objectives, ensuring high standards of accuracy and consistency.
M.Sc in Plant Biotechnology, Biochemistry, Botany, with Three Years Research Experience OR Doctoral Degree in Biotechnology, Biochemistry, Botany. Experience of working in plant tissue culture and transformation, molecular biology techniques and plant genome editing.
The Manager Drug Safety Content Analysis will manage and supervise project’s PV Operations/training staff on a day-to-day basis, guiding performance of PV Operations staff in ongoing projects in terms of training, quality of deliverables, compliance with the timelines and relevant trainings.