Zoheb uhammad Email & Phone Number | With over 12 years of experience in the medical device industry, I am a passionate and driven leader who strives to deliver high-quality products and services that meet the needs and expectations of customers and stakeholders. I am currently the Director of Regulatory Affairs and Quality Assurance for the Global Generics Emerging Markets division at Dr. Reddy's Laboratories, one of the largest and most respected pharmaceutical companies in India and the world. In this role, I oversee the quality and regulatory aspects of a diverse portfolio of products, including invitro diagnostics, digital therapeutics, artificial intelligence, software as a medical device, and advanced medical devices. I am also responsible for developing and executing the global strategy and vision for these product categories, as well as managing the quality management systems and audits of channel partners across multiple regions. Additionally, I am a PhD Scholar at the Swiss School of Management, where I aim to deepen my knowledge and skills in business administration and management. Some of my core competencies include quality management systems, regulatory compliance, portfolio management, clinical research, risk management, and stakeholder engagement.

Zoheb uhammad

With over 12 years of experience in the medical device industry, I am a passionate and driven leader...
India

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Zoheb uhammad’s Email zoheb_muhammad@in.com

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Zoheb uhammad’s Location India

Zoheb uhammad’s Current Industry Dr Reddys Laboratories

Zoheb uhammad’s Prior Industry Nipro Medical | Edwards Lifesciences | Abbott | St Jude Medical | Clini

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Director Ra & Qa - Global Generics Emerging Markets | Portfolio Management | Global Strategy | Dtx

2022-07-01 00:00:00 - Present

Head - Quality Assurance & Regulatory Affairs

2020-03-01 00:00:00 - 2022-07-01 00:00:00

Quality Assurance Manager - South Asia & South East Asia

2018-11-01 00:00:00 - 2020-01-01 00:00:00

Associate Quality Assurance Manager - India & South Asia

2017-09-01 00:00:00 - 2018-10-01 00:00:00

Clinical Research Associate

2012-04-01 00:00:00 - 2014-05-01 00:00:00

Trainee

2011-05-01 00:00:00 - 2011-12-01 00:00:00

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Zoheb uhammad is a With over 12 years of experience in the medical device industry, I am a passionate and driven leader who strives to deliver high-quality products and services that meet the needs and expectations of customers and stakeholders. I am currently the Director of Regulatory Affairs and Quality Assurance for the Global Generics Emerging Markets division at Dr. Reddy's Laboratories, one of the largest and most respected pharmaceutical companies in India and the world. In this role, I oversee the quality and regulatory aspects of a diverse portfolio of products, including invitro diagnostics, digital therapeutics, artificial intelligence, software as a medical device, and advanced medical devices. I am also responsible for developing and executing the global strategy and vision for these product categories, as well as managing the quality management systems and audits of channel partners across multiple regions. Additionally, I am a PhD Scholar at the Swiss School of Management, where I aim to deepen my knowledge and skills in business administration and management. Some of my core competencies include quality management systems, regulatory compliance, portfolio management, clinical research, risk management, and stakeholder engagement.

Zoheb uhammad has prior
experience in the following industries:
Nipro Medical | Edwards Lifesciences | Abbott | St Jude Medical | Clini

Zoheb uhammad has the following professional experience:
Dr Reddys Laboratories | Nipro Medical | Edwards Lifesciences | Abbott | St Jude Medical | Clini