Udaykumar Rakibe

Founder @Pharmamantratm

Nashik, MH, IN
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Aug 2017 — Present

Founder @Pharmamantratm

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Nashik, IN

Udaykumar is a quality professional with a dynamic career steering organization through complex Quality & Regulatory challenges, transitions, building an empowered and talented workforce in the cross-cultural environment within highly competitive products and regulatory environment. In Year 2006, as Director - Quality Assurance, he was mandated and given the task to execute and spearhead the proactive remediation at Ranbaxy Lab. Ltd. Subsequently since Daichii Sankyo takeover, he was made Head, India and Asia Quality Operations and overseeing the state of control. In late 2011 he was recruited by Intas Pharma Ltd. to create a self-sustaining quality management system. Further, in 2013 he was hand-picked & recruited by Wockhardt Ltd, as Senior Vice President – Quality, to turn around the Quality Management, lead and manage the remediation of Quality initiatives. He has represented the Organisation as Quality Head and prepared, presented and attended the regulatory meetings with IAG/ MHRA/ IMB/ USFDA at London and Washington. Has performed 400+ Audits and faced 500+ regulatory audits.He has founded the consulting firm, PharmaMantra, a Quality Advisory and consulting firm in August 2017. Since then he has performed Training, GAP assessment Audit, Site support during EDQM/ USFDA, Toxicological PDE Certification, and Consulting assignments for Indian and MNC clientele. He has proposed Corrective Action Plan and worked with senior management to maintain a culture of compliance and trust with regulators. He envisions thorough PharmaMantra, he shall be able to provide the Manufacturing and Quality Leaders the desired insights and advice to reach simple sustainable solutions for the seemingly complex situations/ problems/ activities. He has experience which can be shared and adopted for various stages of the Quality System developments and subsequent evolution to demonstrate the desired Culture of Pharmaceutical Quality.

EDUCATION

1983 — 1985

Gokhale Edcuation Societys H.P.T.Arts & R.Y.K.Science College, Vidyanagar, Nashik 422005

HSC, Biology/Biological Sciences, General

1985 — 1991

Gokhale Edcuation Societys H.P.T.Arts & R.Y.K.Science College, Vidyanagar, Nashik 422005

B.Pharmacy and M. Pharmacy, Pharmaceutics

1992 — 1994

J.D.C.Bytco Institute of Management Studies & Research, Nashik 422005

MBA, Logistics, Materials, and Supply Chain Management

1976 — 1977

Kendriya Vidyalaya

CRPF, Jhadoda Kalan, Class Fourth, Middle

2014 — 2019

Dr. Babasaheb Ambedkar Marathwada University, Aurangabad

UDCT- Doctor of Philosophy Ph.D., Pharmacy

1972 — 1976

Kendriya Vidyalaya

Janakpuri, N. Delhi, First to Third, Middle

1980 — 1981

Kendriya Vidyalaya

Bhatinda Cantt. Eighth and Ninth, Middle School

1971 — 1972

Kinder Garten Air Firce Station, Palam, N. Delhi

Pre-schooling, Elimentry

1982 — 1983

Kendriya Vidyalaya

Ojhar SSC, Tenth in School, SSC

1977 — 1980

Kendriya Vidyalaya

Vayusena Nagar, Nagpur, Fouth to Eighth, Middle School

ABOUT UDAYKUMAR RAKIBE

Demonstrated track record, by leading cross functional global teams to achieve desired tactical, strategic business objectives with continued assurance of product quality and GMP compliance. Proven expertise in defining organizational structure for Quality Management and align Quality function with the Business objectives/ goals. Articulate communicator, highly skilled influencer, negotiator. Identified and streamlined Quality System - Harmonisation and Digitisation. A highly motivated result oriented professional with about three decades domain experience in the pharmaceutical quality management in regulatory GXP/GMP arena. Spearheaded the task of developing, formulating and implementing a global remediation plan & strategy. An accomplished professional, worked in WL & Import Alert remediation and CAP. In past one decade faced and participated in 450+ Regulatory Audits, and in the corporate role globally performed 400+ due diligence/ Audits. Enabled, trained and empowered operations teams to steer through the regulatory challenges posed by ever increasing expectations of MHRA/ EU & US-FDA.Value – • Trustworthy, Truthful, Honest • Dependable, committed to excellenceSkills –• Instilling Culture of Pharmaceutical Quality• Mentorship & Leadership, Articulate Communicator, Listener & Influencer• Strategic thinking & task orientation for remediation activitiesDeliverables –• Lead and mentored large teams, with supervising 10+ direct reports• Building Strategic planning and execution of plans, project management• Planning and Leading regulatory and vendor/ supplier audits• Review and development of Quality Management Systems• Budgeting and controlling, Budget of the 3rd party and contract manufacturing• Developing and Launching new products with 3rd party RnD and operations team• Training and development, Organising workshops Guidelines for 3rd party/ partners

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