Christophe Mellon

Chief Executive Officer at giiant pharma inc.
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Location
Lévis, Quebec, Canada, CA
Languages
  • French -
  • Spanish (conversational) -

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Experience

    • Canada
    • Research
    • Chief Executive Officer
      • Jan 2023 - Present

      Energic and visionary leader that seeks to leverage science for the common benefits of investors and patients.

    • Vice President Discovery & Chemistry
      • Jul 2021 - Present

      My role is to lead and coordinate pre-clinical group efforts to ensure timely progress from establishing early discovery work to pre-clinical package data acquisition. I guide diverse people with different scientific and cultural backgrounds towards a unique well-defined goal. I believe sharing information and opinions is a great way to generate engagement, to increase company savviness and insure quality of work.

    • Canada
    • Chemical Manufacturing
    • 1 - 100 Employee
    • General Manager
      • Feb 2020 - Jul 2021

      As a general manager of a small company, I was intimately involved in defining strategy over the next few years and the tactics needed to deliver significative milestones. I was defining science, orienting marketing, controlling production, ensuring regulatory progress and preparing sales efforts. As a general manager of a small company, I was intimately involved in defining strategy over the next few years and the tactics needed to deliver significative milestones. I was defining science, orienting marketing, controlling production, ensuring regulatory progress and preparing sales efforts.

    • Project Manager RnD
      • Oct 2015 - Feb 2020

      Coordinate and implement the necessary steps to deliver on various goals in RnD.

    • Contractor
      • Apr 2015 - Sep 2015

      Explore conditions to deliver a new type of silica gel.

    • United Kingdom
    • Chemical Manufacturing
    • 1 - 100 Employee
    • Associate Director
      • Mar 2013 - Sep 2014

      Supervise a team of 20 people including 3 group leaders for production of pharmaceuticals in the context of contract services. Recruiting from contact to interview completion. Manage logistics in the facility. Improve laboratory design and function. Oversee Safety. Manage budget and perform instruments acquisitions. Main contact with clients internationally. Ensure quality and speed of delivery. Revise certificates of analysis and prepare shipments. Seek to create and sustain employee engagement. Show less

    • Group Leader in Organic Synthesis
      • Aug 2010 - Mar 2013

      Supervise a team of 15 people for production of pharmaceuticals in the context of contract services. Manages logistics in the facility. Main contact with client internationally. Ensure quality and speed of delivery. Revise certificates of analysis and prepare shippings.

    • Founder
      • Feb 2010 - Apr 2011

      Advise pharma and biotech companies on issues related to ADME, pharmacokinetics, formulation, relevance of in vitro and in vivo testing, synthetic chemistry, analytical chemistry, intellectual properties and licensing. Special expertise in controlled experiment for testing hypotheses. Advise pharma and biotech companies on issues related to ADME, pharmacokinetics, formulation, relevance of in vitro and in vivo testing, synthetic chemistry, analytical chemistry, intellectual properties and licensing. Special expertise in controlled experiment for testing hypotheses.

    • Canada
    • Biotechnology Research
    • Associate Director
      • Jun 2008 - Nov 2009

      Reporting to COO, lead and manage internal organic and analytical chemistry (people and budget) as well as establish external research partnerships. Guide 2-5 employees in China. Synergize with local CROs. Supervise internal metabolism projects, pharmacokinetic studies and formulation development. Create IP. Support regulatory group. Active role in manufacturing of GMP API. Reporting to COO, lead and manage internal organic and analytical chemistry (people and budget) as well as establish external research partnerships. Guide 2-5 employees in China. Synergize with local CROs. Supervise internal metabolism projects, pharmacokinetic studies and formulation development. Create IP. Support regulatory group. Active role in manufacturing of GMP API.

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Research Fellow
      • Jun 1999 - Jun 2008

      Managed up to 3 employees. Invented and profiled molecules in osteoporosis, pain, respiratory, hypertension, tropical disease working on enzymes, kinases and receptors. Special strengths in new analytical methods of biosamples and in accelerating proof of concepts in animals. Strong metabolism background. Experience in radiosynthesis. LC-MS reference for organic chemists. Managed up to 3 employees. Invented and profiled molecules in osteoporosis, pain, respiratory, hypertension, tropical disease working on enzymes, kinases and receptors. Special strengths in new analytical methods of biosamples and in accelerating proof of concepts in animals. Strong metabolism background. Experience in radiosynthesis. LC-MS reference for organic chemists.

Education

  • Massachusetts Institute of Technology
    PostDoc, Organic Chemsitry
    1997 - 1999
  • Université de Montréal
    Ph. D., Organic Chemistry
    1992 - 1998
  • Université Laval / Laval University
    Bachelor of Science (B.Sc.), Chemistry
    1988 - 1992

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