Started working as an Assistant Manager - Business Development at VIMTA LABS. Taking care of all the Business Development work for Europe, China and India market. Our service portfolio includes Clinical Research Services, Preclinical Services and cGMP Analytical services for small & large molecules. Our team of 1100+ professionals constantly endeavor to provide timely scientific solutions and services to help customers manage their drug development and manufacturing processes more efficiently, without compromising on quality.Long track record of successful global regulatory audits from national and international regulatory authorities (DCGI, US FDA, UK MHRA & other European countries, NPRA etc),In addition to the vast experience in simple BA/BE studies, VIMTA specializes in Complex design studies, First-to-file submissions, Studies on complex molecules (highly variable drugs), Studies in special populations, patient based studies, 505 b(2) submissions, Studies on different dosage forms – e.g., injectable, ODS, patches, oral suspensions, topical etc. and studies with higher sample size (>100 subjects)

1. As Sr. Manager - Business Development for Contract Development and Manufacturing for Small Volume Parentals : Liquid Injections - Ampoules and Vials and Lyophilised Injections - Auto Loading/unloading in Vials and Cephalosporins (Tablet, Capsule, Sachet, Dry Syrup, Dry Powder injections) and Oral Liquids (pet and glass bottles) for Europe, UK, Canada and GCC Markets. 2. Seeking Customers for Different Business Models through our EU GMP Approved Manufacturing Facility for Small Volume Parentals - Liquid and Lyophilised Injections. 3. Working with R & D team to successfully develop Generic Products and then pitching the customers to participate as Sakar as a CMO. 4.Working with project management team to plan and execute the scope from planning and budgeting, planning/scheduling with development and functional groups, monitoring the execution of activities with internal and cross company technical team.5. Expertise in handling out-licensing as well as technology transfer projects of contract manufacturing.6. Sales achievement & tracking against the planned budget for Contract Manufacturing & Out-licensing portfolio.7. Business Development Activities for US Market with anti-cancer range of products Oncology, the set up includes : An up-to-date Analytical Development Lab, Formulation Development Lab, R & D Lab Active Pharmaceutical Ingredient (API) manufacturing unit Formulation unit for Oral Solid Dosage (Tablets & Capsules) Formulation unit for Liquid & Lyophilised Injections

1. Business Development for Formulation and Development for USA / Canada, Europe for In house Products.2. Effective & timely execution and maintain R & D programme management.Responsible for lead generation, sales and business development for above regions.3. Taking care of business of product development, Technology transfer, dossier preparation, contract manufacturing and licensing.