Chairman & Managing Director

• Jun 2012 - Present

www.gjnaturecareandenergy.comG J Nature Care & Energy Limited is an Indian based waste to energy solution providers with excellent local knowledge of Municipal Solid Waste (MSW) problems and convert the waste problem into an energy solution for the society and the betterment of our environment. We are allied with two British companies, Biomass Power Limited &London Investment Consultancy Limited to provide ‘Waste to Energy Solutions from Municipal Solid Waste.We design, install and operate the plant having highly optimized and proven technology of staged gasification with steam cycle, which ensures to meet the criteria of advanced conversion technology without any technological risk. Extensive in­house computerized fluid dynamics simulation and analysing capability enable us to achieve maximum energy output from significantly varied, unsorted and high moisture containing municipal waste with minimal landfill ash generation. Our design of combined heat and power system efficiently utilizes the energy from steam. We process the waste with excellent emission controls and minimal residue discharge.We consider the waste as a precious resource and let us convert it to green energy. We have 120 years of combined experience in waste to energy projects all over the world. Our team of young professionals and experienced technical experts will deliver the technology innovating green energy concepts.

Managing Director

• 2012 - Present

www.gmpcom.comQualified Person service, Pharmaceutical management consultancy, Pharmaceutical technology solution provider, Quality management facilitation, Regulatory compliance certification and technology transfer management. Specialist in pharma manufacturing services. We are a team of 30+ in-house consultants. We are a team of highly skilled and passionate individuals who together offer a valuable support and consultancy service to the pharmaceutical and food supplement industry. We truly love what we do.And it shows. We get it right in an industry where getting it wrong is not an option. Ourclients feel secure in the knowledge that we have the right experience, qualifications anddrive to deliver the right results.Our team is everything and we are constantly improving and growing. Although we exist ina world of process and procedure we strongly believe that people are our most importantresource.• Have an excellent track record since start up• Exceeded project and financial objective of the company by 50% in the past • Have confirmed projects from market leading global Pharmaceutical manufacturing companies

Director

• 2012 - Present

www.gpmcuk.comGPMC provides the major operators in oil, gas and renewable energy sectors with specifically engineered solutions, support and project management. The use of our highly specialized software and strategic partnerships with renowned companies in these fields has made GPMC one of the most competent engineering solution providers in the energy industry. We aim to provide offshore vessel operators, installation contractors, vessel owners and other stakeholders in this industry with all the required engineering assistance to ensure their projects are successful and completed on time.

Chief Executive Officer

• Feb 2016 - Present

www.gjecopower.com

Head of QA & QP

• 2013 - 2015

Heading site quality and compliance team to facilitate site closure and transfer of products to CMO. Actively working with Merck CH and Seven Seas board to establish effective future QA organisation.

Quality Compliance Manager & QP

• 2010 - 2012

RB’s flagship manufacturing site with over 130 different formulations ranging from Sterile injection, Tablets, Capsules, Sachets, Oral liquids, Creams, Gels, Ointment and antiseptic liquids. Significant experience of pharmaceutical manufacturing operations, supply chain management and I have excellent understanding of the EU and international GxP regulations. Successfully developed a strong quality compliance function which gained first time site approval from stringent regulatory bodies like ANVISA and FDA. Key roles & responsibilities• Heads site quality compliance activities • Site quality and compliance strategy development, implementation and monitoring • Management of Regulatory audits (MHRA, FDA, ANVISA etc)• Management of Customer complaints system, PQRs, Stability, Internal audits and ISO certification • Responsible for Vender management system and external audits • Training and coaching for site quality, technical and operation team in GMP, GDP, Technical and Validation activities. • Site Quality and compliance improvement champion • Technical consultation and Quality & compliance support for other international RB sites • Releasing QP and facilitate QP training process • Regulatory documentation review process and QP declarations

Quality Improvement Manager

• 2008 - 2010

• Generate Quality Improvement Strategy and implementation• Site preparation and approval for ANVISA , FDA , Tai FDA and Korean FDA • Generation of comprehensive GMP & Technical training and competency assessment system. • Provide Quality Management coaching for site leadership team members • Quality KPI generation and implementation of effective systems to evaluate performance • Site Quality Leader responsible to influence senior management to facilitate GMP improvement CAPEX • Coordination of site QP training and QP succession plan generation • Review and re-design of area quality leaders roles and responsibilities

Research Scientist

• Aug 2001 - Aug 2002

Operations Manager

• Aug 1997 - Aug 1999

Project Management and Export based API manufacturing facility operation