David Muller

Associate Director, Pipeline Products. Technical Operations & CMC at Tarsus Pharmaceuticals, Inc.
  • Claim this Profile
Contact Information
us****@****om
(386) 825-5501
Location
Irvine, California, United States, US
Languages
  • French -

Topline Score

Topline score feature will be out soon.

Bio

Generated by
Topline AI

5.0

/5.0
/ Based on 2 ratings
  • (2)
  • (0)
  • (0)
  • (0)
  • (0)

Filter reviews by:

SUKHON LIKITLERSUANG

As David's teammate at Par Pharmaceuticals for the past two and a half years, David is diligent and highly committed to his work. I've benefited from his problem-solving, tireless work ethic, and willingness to do whatever it takes to achieve project milestone that will translate the company's vision into reality. As a colleague, David is incredibly generous with his time and expertise, which includes everything from many years of pharmaceutical experience to expert-level knowledge of solid dosage form technology. Regardless of deadlines or other pressure, David always delivers. His superior organizational skills make him the consummate multi-taker.

Benoit Schmitt

Davis has an extensive knowledge of the ingredient, processes, process optimization used in the pharmaceutical industry. David did show good excellent interdisciplinary skills and interpersonnal qualities.

You need to have a working account to view this content.
You need to have a working account to view this content.

Experience

    • United States
    • Pharmaceutical Manufacturing
    • 100 - 200 Employee
    • Associate Director, Pipeline Products. Technical Operations & CMC
      • Feb 2023 - Present

    • Sr. Manager Pharmaceutical Sciences
      • Aug 2021 - Feb 2023

    • United States
    • Biotechnology Research
    • 200 - 300 Employee
    • Associate Director of Formulation Development
      • Mar 2021 - Aug 2021

    • Ireland
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Manager, Technical Services
      • Jul 2015 - Mar 2021

      - Scale-Up activities at PAR Irvine. - Implementation of QbD approach in projects. - Implementation of Six-Sigma Lean in projects. - Use of SAS JMP to modelize the process steps and optimize them. - Scale-Up activities at PAR Irvine. - Implementation of QbD approach in projects. - Implementation of Six-Sigma Lean in projects. - Use of SAS JMP to modelize the process steps and optimize them.

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Sr Process Engineer
      • Jan 2013 - Jul 2015

    • Senior Scientist, Formulation and Development
      • Jul 1999 - Sep 2012

      Development of modified release forms. Development of chewable and immediate release tablets. Development of improved bio-availability formulas. Development of generics. Development of Analytical method and establisment of In-Vitro/ In-Vivo correlations. Analysis of Clinical results and implement formulation/ process change accordingly. Development of modified release forms. Development of chewable and immediate release tablets. Development of improved bio-availability formulas. Development of generics. Development of Analytical method and establisment of In-Vitro/ In-Vivo correlations. Analysis of Clinical results and implement formulation/ process change accordingly.

    • Formulation Scientist
      • May 1998 - Jul 1999

      Development of extended release matrix formulations. Development of analytical methods to test the dosage form. Development of extended release matrix formulations. Development of analytical methods to test the dosage form.

Education

  • Universite Paris XI
    DEA (Master 2), Biopharmacy, Pharmaceutical Technology
    1997 - 1998
  • University of Strasbourg
    Pharm D., Industrial and Physical Pharmacy and Cosmetic Sciences
    1990 - 1998
  • University of Strasbourg
    Master of Science - MS, Pharmacy, Industrial Pharmacy
    1996 - 1997

Community

You need to have a working account to view this content. Click here to join now