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Mrs. Savita Gowda, Managing Director, aged 37 years, is a Graduate in B.Sc. (Chemistry). MBA in 1999 from Newport University , California (USA). She has over 14 years experience in manufacturing and marketing of Drug Intermediates & Bulk Drugs. She worked for M/s. Menon Pharma Pvt. Ltd. as Product development Chemist for 3 ½ years, between 1991 to 1994. She is today in charge of local & international marketing. She has played multiple roles during the last 14 years in transforming Sharon from a small 'Me Too' Company to a multi-product and multi-service provider across the Pharma Value Chain. Her expertise in Marketing and Supply Chain Management has ensured that Sharon has a very high customer retention. In the past she has not only achieved but at times surpassed Targets set forth for her. During the journey of Sharon so far, she has ensured that high levels of business ethics are imbedded into all working at Sharon and ensured that at all times the long term objectives are addressed to during decision making. Her visionary approach and indepth understanding of market dynamics reflects in decisions which led to
Sharon 's forward integration into Formulations contract manufacturing for regulated markets.
Mr. Mohan P. Kala, Non Executive Director aged 47 years is a Chartered Accountant. He also completed M.A. (Economics) from H. N. Bahuguna University , Srinagar in the year 1981. He has experience in the field of pharmaceuticals for the last 15 years and in finance, costing and tax matters for the last 25 years. He was also one of the promoters of M/s. Kilitch Drugs (I) Ltd. The company is extremely benefited form his wide experience & expertise in the area of Finance, Banking & Taxation. In SHARON he looks after the finance, costing and taxation matters. He is also in the Managing Committee at Andheri Recreation Club , Andheri(w), Mumbai as elected member for last 6 years.
Mr. Lalit Misra, Whole Time Director, aged 31 years is a Post Graduate in Business Administration from Derbyshire Business School , United Kingdom & a Graduate in B.E. (Chemical). He has over 8 years experience in Operations, Projects & Business Development. He is responsible for Operations, Business Development and New Projects in the organization. He is among the new breed of young entrepreneurs who believes in innovations & fresh ideas of modeling business for long term sustainability. He has contributed in setting up Shaorn's Taloja Facility, which is highly efficient for multiproduct handling. Transforming Ideas into Strategies thereafter into realities has been his focus in Sharon . He is currently leading the transformation of the Company from being recognized as reliable supplier of Intermediates & API's to being a force to reckon with throughout the Value Chain right trough from Development & Manufacturing of Intermediates, API and Formulations. His objectives in the Operations Management include (a) creating system driven processes which reduce risks of Human error, (b) product delivery with high process efficiency coupled along with optimum utilization of resources, (c) Speed on delivery of new products and (d) ensuring high motivation levels in his Team. His belief is that Quality Certifications are purely tools that improve business results and not Marketing Tools.
Mr. Vijay L. Kirpalani, Whole Time Director, aged 50 years, has done his B.E. in Chemical. He has around 25 years of experience in Designing, Executing & Engineering of Projects, Product Development, Technology development, Feasibility Study of the Projects. He was associated with the following organizations namely BARC, Bharat Petroleum Corporation, United Phosphorous and IPCL & Baroda Productivity Council. Further he has also worked with the following International Companies namely B.I.L. Chem Ltd .(Bangladesh), POLSERVICE(Poland),Egis Pharmaceuticals(Hungary), Fermion, O.Y. (Finland), Gist Brocades (Holland), Inter Chem Technical Associates(USA), Synthon Corp(USA), Green Valleys Estb.(Oman),Thomas H. Barton & Co.(USA.)..
Dr. Vivekanand N. Badoni, Independent Non-Executive Director aged 41 years, has done his M.Sc in Chemistry and Ph.d in Organic Chemistry. He had worked on a research project "A Study of thermal degradation and stabilization of NYLON-6" and was involved in Research and Development activities in the field of Engineering Plastics and their degradation kinetics. He has a total work experience of 14 years in production of bulk drugs, drug intermediates and fine chemicals. He has worked with M/s. Dorf Ketal Chemical (I) (P) Limited as Dy. General Manager (Production) looking after production of Antioxidants, Corrosion Inhibitor, Antifaolants, Antisclalants etc. used in Refinery and Petrochemicals. He then worked with M/s. Kapoor Latex (P) (L), Kanpur as an Officer (R&D) from 1990 to 1991, M/s. Siddharth Carbochem (P) (L) as Asst. Production Manager from 1992 to 1993 and later with M/s. Dhupar Chemicals (P) (L) as Production In charge from 1994 to 1995.
Dr. Nivvedita Patil Kartik, Independent Non-Executive Director, aged 33 years, has done her Bachelor of Medicine and Surgery and Diploma in Ophthalmic Medicine & Surgery. She is a Consultant Opthalmic Surgeon at Krishna Eye Care. She is one of the founder members of Thane City Laser Eye Centre, honorary ophthalmologist at Red Cross Society of India and is also involved in Clinical Research by as a co-investigator on global clinical research projects. She was associated with Surya Eye Tech as an Assistant Opthalmic Consutant. She has been one of the lecturer at Novartis Limited and FDC Private Limited for Diagnosal of Glaucoma (Basics), Dry-Eye and Occular Infections respectively.
Mr. Sanjay Shah, Independent Non-Executive Director, aged 57 years, has done M.Sc. in Research and B.Sc. ( Physics & Chemisrty) . He has also done course of ISO-9000 QMS.
He has more than 30 years of experience in Quality System , in auditing and determining the adequacy, effectiveness, and degree of the company's compliance to the standards and regulations: ISO 9001, ISO 13485, MDD/93/42, US FDA 510k, Quality System Regulations & WHO GMP / c-GMP, Regulatory Consultant in CE certification and US FDA 510k regulations regarding the manufacture of medical devices and GMP certification regulations regarding manufacture of Medical Devices, Active Pharmaceutical Ingredients (Bulk Drugs), Pharmaceuticals Formulations and Sterile Devices and expertise in preparation of Quality Manuals, Policies, Standard Operating Procedures, Technical Master File, Drug Master File (DMF) for API and regulatory submissions. |
