Francisco Gamboa Email & Phone Number | I am a Hub Submission Manager at Pfizer, where I manage the development, quality control, and publication of multiple submission types for new registration of drugs and medical products in the Africa & Middle East region. I have a Specialist degree in Health Audit and a Bachelor's degree in Biomedical Engineering, which give me a strong knowledge of the drug development process, regulatory affairs, clinical trial applications, and submission management. In my role, I drive adherence to external regulatory guidelines and compliance timelines, provide strategic direction to teams on regulatory logistics, and serve as a regulatory operational liaison on the project team throughout the product lifecycle. I have also gained deep experience in CMC regulatory documentation, regulatory strategy, dossier management, CTD & eCTD submissions, and new registration dossiers. I am characterized by good organizational skills, excellent team management, and effective communication skills with teams and customers. I am motivated by the opportunity to contribute to the health and well-being of people around the world through innovative and quality solutions.

Francisco Gamboa

I am a Hub Submission Manager at Pfizer, where I manage the development, quality control, and public...
Sandwich, England, United Kingdom

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Francisco Gamboa’s Location Sandwich, England, United Kingdom

Francisco Gamboa’s Current Industry Pfizer

Francisco Gamboa’s Prior Industry Baxter Healthcare | Navitas Life Sciences | Imexhs | Datamedic | Ese Hospital Universitario De La Samaritana

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Francisco Gamboa is a I am a Hub Submission Manager at Pfizer, where I manage the development, quality control, and publication of multiple submission types for new registration of drugs and medical products in the Africa & Middle East region. I have a Specialist degree in Health Audit and a Bachelor's degree in Biomedical Engineering, which give me a strong knowledge of the drug development process, regulatory affairs, clinical trial applications, and submission management. In my role, I drive adherence to external regulatory guidelines and compliance timelines, provide strategic direction to teams on regulatory logistics, and serve as a regulatory operational liaison on the project team throughout the product lifecycle. I have also gained deep experience in CMC regulatory documentation, regulatory strategy, dossier management, CTD & eCTD submissions, and new registration dossiers. I am characterized by good organizational skills, excellent team management, and effective communication skills with teams and customers. I am motivated by the opportunity to contribute to the health and well-being of people around the world through innovative and quality solutions.

Francisco Gamboa has prior
experience in the following industries:
Baxter Healthcare | Navitas Life Sciences | Imexhs | Datamedic | Ese Hospital Universitario De La Samaritana

Francisco Gamboa has the following professional experience:
Pfizer | Baxter Healthcare | Navitas Life Sciences | Imexhs | Datamedic | Ese Hospital Universitario De La Samaritana