Mr. Peter Bains is the Director of Syngene, since 2011.
Peter has more than two decades of experience in the global pharmaceutical space. With strategic and operational leadership expertise across geographies, functions and business segments, he brings a global perspective with a forte in emerging markets, particularly China and India.
Peter has implemented strategic goals and objectives for Syngene and enables the Board of Directors to fulfil its governance function. In addition, he also directs and leads us towards the achievement of Syngene's philosophy, mission and strategy.
Before his appointment to the Board of Syngene in 2010, Peter had a 23-year career at GlaxoSmithKline, where he held several roles including Head of Global Marketing and Senior VP of Commercial Development (International). During his tenure, he helped establish several GSK brands as brand leaders and conceived, developed and implemented an organizational redesign in GSK's International Region.
From 2009, he has been a consultant specialising in supporting strategic growth opportunities in small- and medium-sized innovation-based life science companies.
Peter completed his B.Sc Combined Honours in Physiology/ Zoology from Sheffield University. During his spare time, he enjoys spending time with his family and is a keen sports enthusiast.
Dr. Manoj Nerurkar is the Chief Operating Officer of Syngene since April 2012. He joined Syngene in 2009 to head the Formulation Development Center, and was the Vice President & Head - Small Molecule Discovery & Development till March 2012.
As the head of the senior leadership team of scientific department, business development and project management, Manoj has been instrumental in terms of both strategic leadership and operational management in underpinning Syngene's recent growth and evolution. He is also responsible for implementing the strategies for growth and enabling operational excellence across Syngene.
He identifies and builds new business opportunities to maintain the company's market leadership position and profitability. He is working with the Syngene Board of Directors to bring future opportunities to fruition through adequate investment in new infrastructure and technologies.
Manoj has extensive experience in the development of oral solid & injectable dosage forms from Phase I to commercialization. Prior to joining Syngene, Manoj worked for Novartis and was responsible for setting up their Drug Development R&D center in India.
Manoj has also worked with Bristol-Myers Squibb in New Jersey, for 12 years, where he had the opportunity to work on the development of various dosage forms including immediate and modified release tablets, capsules, and conventional and depot injectable formulations of small and biological molecules. He has two commercial products to his credit which include an intravenous formulation of BMS' first biologic molecule - Orencia and an intramuscular formulation of an anti-schizophrenic drug - Abilify.
Manoj obtained his PhD in Pharmaceutical Chemistry from University of Kansas, and has completed a Management Program from the Wharton School of Business. He holds several patents in the Formulation Development area and has several publications to his credit in international peer-reviewed journals.
Mr. Chinappa is the President - Finance, Syngene as of April 2008. Prior to this, he was the Vice President - Finance, Biocon Limited since 2004.
He joined the company as Senior Manager - Finance in 1999 and has over 20+ years of experience.
Chinappa oversees all the finance and fiscal management of company operations, and is responsible for the overall management and direction of the company. He provides leadership and coordination in the administrative, business planning, accounting and budgeting efforts of the company. As a member of the senior leadership team, he also plays an important role on all strategic and tactical matters as they relate to budget management, cost benefit analysis, forecasting needs and the securing of new funding.
He has been instrumental in setting up various EOU's and an SEZ. His astute guidance has resulted in the successful acquisition of IP from Nobex, investment and other strategic collaborations with various biotech companies. He has also been an integral part of the team that has engineered the strategic partnership between Syngene and BMS, and other such initiatives to position Biocon as a leading biotech player manufacturing affordable bio-pharmaceuticals.
Mr. Chinappa completed his graduation in Commerce from St. Joseph's College of Commerce, Bangalore in 1989 and Chartered Accountancy from the Institute of Chartered Accountants, India in 1992. Prior to joining Biocon, Chinappa worked with ITC Limited and did his Chartered Accountancy Training with M/s Price WaterhouseCoopers.
Dr. Raman Bakshi joined Syngene in Jan 2010 and is currently heading the Discovery Chemistry division as Vice President. Raman is responsible for driving the various discovery chemistry programs and is one of the most recognized medicinal chemists having over 20 years of experience.
He has extensive experience in the area of drug discovery, medicinal chemistry, organic synthesis, lead design, validation, and optimization, PET ligand design and synthesis, designing intermediates for outsourcing vendors.
Prior to joining Syngene, he was associated with Merck Research Laboratories for over 20 years and worked on various therapeutic areas, including antibacterial, BPH (5- alpha-reductase), Sarcopena (growth hormone scretagogues), diabetes, obesity and other propriety pain and diabetic targets. He has successfully contributed towards several clinical and preclinical candidates like MK-386, MK-493, MK-489, MK-4409 and L-239586.
Raman obtained his Ph.D. under the direction of Prof. Sukh Dev at M. S. University, Baroda and was a Post-doctoral research fellow with Prof. E. J. Corey at Harvard, where he jointly with Prof. Corey discovered the Corey-Bakshi-Shibata (CBS) reagent. Preceding that, he worked with Prof. H. C. Brown at Purdue University where he was also a joint inventor of dicyclohexylchloroborane as a reagent for threo aldol reactions. He has co-authored more than 39 paper and 25 patents.
Dr. Anita Chugh is the Head – Biology and has joined Syngene in 2011, and is responsible for providing the scientific leadership to the different programs at Syngene.
Anita is responsible for the overall management of the Biology function. She has worked operationally for 15 years in discovery biology, spanning both empirical and contract service roles.
She has extensive experience in the area of urology, metabolics and inflammation, and has a track record of identification and progression of candidates to clinics.
Prior to joining Syngene, Anita was associated with Aurigene Discovery Technologies Ltd as Research Director in Discovery Biology and Advinus Therapeutics Pvt Ltd as Senior Director and Head, Biology. She provided leadership to Discovery Biology including screening, molecular-cell biology and in- vivo. Her key responsibilities included scientific guidance, motivating and leading team for preparing and achieving significant success in internal and collaborative research programs, practices, building culture for innovation.
Anita gained her M.Sc. and Ph.D. from the All India Institute of Medical Sciences, and her Post Doctoral Fellowship from McMaster's University in Ontario, Canada, before returning to India in 1995.
She has several published patents and publications to her credit.
Dr. K. S. Rao (B.V.Sc & A.H., M.V.Sc., Ph.D.,) is a Board Certified Toxicologist with more than 35 years of global experience in safety evaluation - toxicology supporting drug discovery & development, agrochemical research and development and is associated with Syngene since May 2011.
He is Emeritus Member of the Society of Toxicology – SOT in US. He is the first Indian Toxicologist to be appointed for this status for being a member of the SOT for 40 years.
Dr. Rao has led multidisciplinary teams in designing/constructing, maintaining, managing of preclinical research – toxicology & animal breeding/stock facilities (to international standards-guidelines, fulfilling Good Laboratory Practice (GLP) requirements) in USA and India.
Dr. Rao has published papers and presented papers in international seminars. He is a member and actively contributed in international organizations in the field of toxicology. He is the principal author of more than 200 safety evaluation study reports of various new compounds marketed or to be marketed. These reports are submitted to various regulatory authorities of several countries, including, FDA & EPA (U.S.A), European, Japanese Health and Indian Regulatory Authorities.
Dr. Dhananjay Patankar joined Syngene in Oct 2010 and currently heads formulation, biologics development and cGMP manufacturing for all biologics (recombinant proteins, antibodies and other macromolecules) as well as drug products (variety of dosage forms for small and large molecules).
In addition, he serves as the Chairman of the Institutional Animal Ethics Committee.
Dhananjay is a Chemical Engineer with 17 years of industry experience in product development, manufacturing and commercialization of recombinant biotherapeutics for Indian and global markets. In his career, Dhananjay has led the development and manufacturing of 7 recombinant biopharmaceuticals that are currently sold in the Indian and other markets.
He has established manufacturing facilities, managed commercial manufacturing operations, and successfully obtained EU-GMP certification for a biologic drug substance and drug product facility. Immediately prior to joining Syngene, Dhananjay led the CMC development of a biosimilar which has recieved Marketing Authorization in Europe, wherein he directly supervised areas such as process characterization and validation, analytical development and validation, product characterization and comparability, and CMC regulatory strategy.
Dhananjay currently serves as Chair of a US Pharmacopeia Expert Committee for Biologics and Member of US Pharmacopeia Council of Experts. He previously served as an industry representative on a National Task Force for establishing regulatory pathway for biosimilars in India.
Prior to joining Syngene, Dhananjay was associated with Intas Biopharmaceuticals Ltd. Ahmedabad, as Chief Operating Officer. He was also associated with the Biotechnology Division of Wockhardt Research Center, Aurangabad as a Sr. Scientist and Group Head for product development and manufacturing.
Dhananjay did his Postdoctoral Fellowship at the Dept. of Chemical and Biochemical Engineering, Rutgers University, Piscataway, NJ (USA). He obtained his Ph.D. (1992) and M.S. (1989) in Chemical Engineering from University of Utah, Salt Lake City and B.Tech. in Chemical Engineering from Indian Institute of Technology, Bombay, 1986.
Dr. Tara Jayaram has been associated with Syngene since 2008 and is currently heading Quality at Syngene.
Tara has been instrumental in setting up an established Quality Department with Quality Control for small & large molecules (DS & DP) and establishing Quality Systems according to cGMP, ICH and international standards including ISO 9001, ISO 14001 & OHSAS 18001.
She has played a key role in getting the GLP Certification by the German GLP Federal Bureau and National GLP Compliance Monitoring Authority (NGCMA), India and is part of Test Facility Management. She has also been a part of AAALAC (Association for Assessment and Accreditation of Laboratory Animal Care) accreditation.
As Head of Quality Department, Tara oversees all aspects of operations within the department, and harmonises and monitors the quality systems throughout the company. She is responsible for liasioning with International and National regulatory authorities. She is also responsible for resolution of the customer complaints, queries and deficiencies, investigation of deviations, batch failures and final disposition.
She has extensive experience in Quality Control, Quality Assurance and Regulatory Affairs. Prior to Syngene, Tara was associated with Biocon as Head of Quality for 20 years and has been the Management Representative/ Management Appointee for ISO 9001, ISO 14001 and OHSAS 18001 certifications. She led Biocon to get various approvals like USFDA, EUGMP, EDQM, ANVISA and many others.
She has been elected as a member of the Executive Committee of Indian Drug Manufacturers Association and is also a member of the Quality Management Subcommittee of Indian Drug Manufacturer's Association (IDMA).
She was also awarded with a Quality Excellence award from IDMA for Biocon.
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