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
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.
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.
Central Medical Services Society has been established with the approval of Cabinet on 24.08.2011 as a Central Procurement Agency to streamline drug procurement and distribution system of Department of Health and Family Welfare, Ministry of Health and Family Welfare, Government of India and to eliminate existing deficiencies.
Development of imine reductase based biocatalytic platoform for the synthesis of chiral amines building blocks for drug discovery and developmental applications