Omair Mehboob

As a highly qualified and experienced pharmacist with a post-graduation degree in Pharmacy, I have developed a deep understanding of the pharmaceutical industry and regulatory environment. With a strong background in business development and regulatory affairs, I am a specialist in medical devices, able to navigate complex regulations to ensure compliance and facilitate market access. I have a proven track record of success in developing strategic plans for product development and launch, managing relationships with key stakeholders, and ensuring regulatory compliance at all stages of the product lifecycle. With my expertise and passion for the pharmaceutical industry, I am dedicated to driving business growth and innovation in the medical device sector.

Experienced Regulatory Professional involved in product registration of medical devices manufacturer (including GE Healthcare, Canon, KA Imaging, Sakura, Canon DelftDI IT, Teleflex, Progetti, e.t.c.) in Pakistan. The product profile ranges from imaging devices, monitoring devices, therapeutic equipment, Software as Medical Device (SaMD), medical furnitures e.t.c. 

Trained ISO 13485 Lead Auditor, EU MDR 2017/745, and ISO 14971

Shirazi Trading Company | Karachi 

Regulatory Affair Specialist I Feb 2017 – Dec 2022

Patients’ Aid Foundation | Karachi 

Procurement & Pharmacy In-Charge I Aug 2016 – Dec 2016

AstraZeneca | Melbourne  

Assistant Product Manager | Jan 2014 – Dec 2015

Muller & Phipps Pakistan Private Limited | Karachi

Regulatory Affair Officer I May 2010 – Sep 2011

Education

PG Diploma in Business Administration & Management 

2014 | Technical Education Australia (Melbourne) 

Masters of Pharmacy 

2013 | Charles Sturt University (Wagga Wagga) 

Doctor of Pharmacy 

2009 | Ziauddin University (Karachi) 

Certification 

ISO 13485 Lead Auditor 

2020 | British Standard Institute (United Kingdom) 

Clinical Research Certified Professional (CRCP)

2016 | Dow University of Health Sciences (Pakistan)