Applications are invited for a walk in interview for recruitment of following positions on contractual basis under the DBT funded project, entitled DBT-NER Advance Level Institutional Biotech Hub at Institute of Advanced Study in Science and Technology Garchuk, Guwahati
Studying the ribosomal RNA diversity, functional relevance of rRNA processing factor 2 in ribosome biogenesis, root, shoot development and drought stress tolerance in rice.
Routine cell culture, differentiation of cells, transfection of cells, lentivirus preparation and transduction, analysis by western blotting, qPCR, ChIP, microscopy, protein purification and various biochemical assays and kits
VBPL is an ISO 13485:2012 and WHO – GMP certified leading global player in Biopharma sector having more than 15 years of operational experience, situated at Hyderabad. We also have offices located in USA. Innovative, ever motivated Research team and uncompromising manufacturing team in providing quality products are our strengths.
Requirement of Manpower for Manufacturing (Vial, Cartridge, PFS & BFS)
Leben Life Sciences Pvt. Ltd is an established pharmaceutical formulation company for more than four decades. LLS has following openings for its EU-GMP Approved Global Standard OSD and Semi-solids Formulation manufacturing facility at Akola
M.Pharma or Ph.D. in any branch of Life Sciences or Biotechnology with at least two peer-reviewed international publication in Science Citation indexed; experience in molecular biology related techniques including PCR, recombinant DNA cloning techniques, plant transformation, and library preparation methodologies for NGS.
Candidate should have the command over the subject with first class throughout the Academics, Good teaching, and professional experience, Published work, such as research papers and technical reports
Experience in conducting/ handling pre-clinical animal studies, expert in cell culture, performing immunological Assays etc. data analysis and report writing. Preference will be given to candidates having experience in working ABSL3/BSL3 facility and small animal handling.
Familiar with cGMP guidelines and Quality Systems as per the international regulatory requirements. Experience in Oral Solid Dosage Manufacturing / CVC Packaging. Exposure to the latest manufacturing and packing techniques.
Define, organize, plan and execute analytical activities and materials characterization of pharmaceutical injectables in compliance with current international/ regional/ national regulations with the support of senior colleagues and team members.
M.Pharm or Ph.D; Manage R&D development related operations for specific dosage forms to ensure on-time, within budget quality delivery along with a continuous focus on improvements
Quality guidelines mentioned by FDA, MHRA, and other regulatory bodies; GxP practices and GAMP5 guidelines. As a part of our Risk Advisory team you will build and nurture positive working relationships with teams and clients with the intention to exceed client expectations.
IIT Delhi lays a strong emphasis on the sponsored research and industrial interaction. The Institute has not only given due emphasis to investigation of problem of direct relevance to the needs of the country through time bound sponsored and consultancy project aimed at solving live industrial problems, but also has given special attention to emerging areas internationally.