Francis Dumont Email and Phone Number
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I am an independent pharmaceutical development professional offering advisory and consultative support focused in the areas of 1) sourcing analysis and implementation; 2) CDMO business development; 3) clinical development through commercialization approaches; and 4) environmental sustainability. I am a current Advisory Board member at two Southern CA based companies (1) Karmanterra, focusing on innovative climate solutions and (2) AEQUOR, Inc., aiming to solve microbial contamination issues with earth friendly approaches. I retired from Pfizer in 2023 following a wide-ranging 31-year career journey in the Pharmaceutical Sciences organization. My last Pfizer position was Senior Director, Drug Product Supply Strategy, where I had the opportunity to influence many supplier relationships across the development through commercial launch space. My roles have included leadership of global teams and initiatives, accountability for sourcing and manufacturing oversight of products for clinical trial use, direct facility support for clinical scale sterile manufacturing, drug delivery technology evaluation and development, as well as formulation development and analytical characterization responsibilities. Prior to joining Pfizer, I held environmental science positions that included laboratory and on-site characterization and remediation at a multitude of locations across the US. I have been based in Southern CA since 2017 after having spent most of my life on the East Coast, including 25 years at Pfizer's Groton CT site. In addition to my decades of industrial experience, I have a BS degree in Chemistry from Central Connecticut State University. I am looking forward to helping emerging companies and their products reach their full potential through innovative collaborations and approaches.
Atlantic Environmental Science
View- Website:
- aequorinc.com
- Employees:
- 9
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Environmental ScientistAtlantic Environmental ScienceCarlsbad, Ca, Us
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Advisory Board MemberAequor, Inc. May 2024 - PresentCalifornia, United StatesDevoted to developing innovative and sustainable solutions for a range of markets related to Healthcare, Antibiofilm/Antifouling Treatments and Green Ingredients. -
Advisory Board MemberKarmanterra Jul 2023 - PresentCarlsbad, California, United StatesDedicated to reducing atmospheric carbon dioxide through innovative approaches to agriculture and habitat restoration. -
Independent Advisor And ConsultantSelf-Employed Jul 2023 - PresentHighly experienced and collaborative pharmaceutical professional with broad drug product knowledge leveraging a diverse CMC background that includes strategic sourcing; collaboration management; team and technical leadership; due diligence and integration; dosage form development; clinical drug product manufacturing; environmental sustainability, and Good Manufacturing Practices (GMP).
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Pfizer Retired- More To Come....To Be Determined Apr 2023 - Jul 2023 -
Senior Director, External Drug Product Supply StrategyPfizer May 2019 - Apr 2023La Jolla, CaCurrent areas of focus include strategic sourcing, vendor relationship management, and integration process improvement within the clinical drug product manufacturing space. -
Senior Director, Drug Product Supply SourcingPfizer Pharmaceuticals Aug 2010 - May 2019Perform line management responsibilities for Clinical Sourcing department. Directly lead or participate in sourcing and process related initiatives as needed. Examples include a process initiative for delivering novel, externally manufactured capsules and an Emerging Market vendor landscape initiative. Represent group on multiple Leadership Teams and Quality Councils. Lead and assure appropriate communication to partner lines including Procurement, Quality, Technology & Strategic Sourcing -
Clinical Supply Sourcing LeadPfizer Global Research & Development Jun 2007 - Aug 2010Oversee individual contributions towards Sourcing Specialist and Manufacturing Coordinator roles of direct reports.Develop colleagues through coaching, feedback, joint problem solving, and supporting training opportunities.Lead performance management activities for group.Lead cross-functional teams responsible for outsourcing initiatives related to drug product manufacturing. Examples include implementing an aseptic vendor strategy and Asian supplier initiatives.Assure vendor readiness to support Pfizer drug product portfolio needs, including in-licensed and acquired compounds.Interact with global teams to understand and address project challenges.Work with Procurement, Strategic Alliances, Legal, and Quality to secure appropriate agreements with vendors.Define and implement vendor management processes.Drive continuous improvement of internal practices pertaining to external manufacturing. -
Sourcing SpecialistPfizer Global Research & Development Jan 2006 - May 2007Managed external drug product manufacturing vendor base to support Global portfolio.Focused on liquid drug products (sterile and non-sterile).Evaluated vendors to support drug products that cannot be delivered through internal capabilities/capacities.Worked with Quality Assurance (QA) group to qualify vendors; served as subject matter expert at audits.Based on project needs, directly coordinated external manufacturing activities, including batch records review/approvals and in-plant oversight.Represented Supply Chain on Pharmaceutical Sciences Integration Team related to acquisition of a Biologics-based company.Led drug product supply integration efforts and coordinated initial drug product manufacturing campaigns following acquisition.Managed a consultant performing background activities to support external manufacturing.
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Senior ScientistPfizer Nov 2003 - Jan 2006Assured cGMP and SOP compliance by LDM area and personnel.Responsible for update, maintenance, and development of SOPs.Responsible for training, including strategy development/implementation.Member of team that rolled out training on standardized global procedures.Served as primary contact point with QA organization.Coordinated and authored audit responses and quality investigations.Supported external manufactures, including batch record reviews and in-plant oversight.Led formation of inaugural Drug Product Manufacturing Safety Committee and served as Chair during 2004.Led formation of inaugural Technology & Compliance Awareness Team and served as Chair during 2005.Participated in numerous project and workstream-related teams, including PGE2 Pharm Sci Project Team, Drug Product-Quality Assurance Forum, Sterile Network, and Drug Product Staff Meetings.Supported validation programs.Reviewed and authored various qualification protocols.Worked with multiple lines to assure appropriate review, sign-off, and execution of protocols, including Microbiology Lab, QA, and Facilities.Managed employee in Summer Student program during 2005. -
ScientistDrug Delivery Technology Assessment Group Feb 2000 - Nov 2003In addition to responsibilities for Associate Scientist:Assumed leadership role as Pharmaceutical Sciences Project Coordinator for a candidate from pre-clinical to Phase 2 development.Responsible for leading team comprised of members from Pharmaceutical R&D, Analytical R&D, Chemistry R&D, QA, Regulatory CMC, and Strategic External Alliance Management.Accepted responsibility for managing a large portion of Pharmaceutical Sciences activities related to Atrix Collaboration.Active member of multiple interdisciplinary, project governing teams.Responsible author for numerous internal status reports.Actively participated in preparing documents for IND filings.Coordinated all Pfizer/Atrix team meetings including teleconferences, videoconferences, and face-to face.Managed/coordinated technical aspects of numerous feasibility programs. Assumed responsibility for budget of several active projects.Established Access database of Drug Delivery contacts.Contributed to internal research initiatives related to parenteral depot systems.
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Associate ScientistPfizer Dec 1998 - Feb 2000Managed/coordinated numerous drug delivery feasibility programs.Evaluated external technologies for applicability to Pfizer programs.Spearheaded development of information management systems for group. -
Associate ScientistPfizer Central Research Feb 1996 - Dec 1998In addition to responsibilities for Assistant Scientist:Independently developed matrix tablet dosage forms through Phase I clinical supplies.Coordinated outsourcing of dissolution testing for matrix tablet project.Communicated matrix tablet development strategy through internal publication.Initiated and coordinated meetings with Solid Dosage Manufacturing related to dosage form nomination.
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Assistant ScientistPfizer May 1992 - Feb 1996Utilized analytical techniques including HPLC Turbochrom data acquisition.Performed formulation techniques including tablet compression, film coating, various granulation methods, and extrusion spheronization.Wrote pertinent sections of Staff Reports.Coordinated tech transfer of several formulations to Solid Dosage Manufacturing area.Participated in formulation transfer and oversight activities for PPD in Brooklyn.Frequently contributed to poster session presentations (internal and external). -
Environmental ChemistAtlantic Environmental Science Jun 1990 - May 1992Conducted soil gas surveys utilizing portable Gas Chromatograph.Performed data validation.Supported contract laboratory selection, including laboratory audits.Authored multiple technical environmental reports.
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Environmental ScientistAtlantic Environmental Science 1990 - 1992
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Analytical ChemistEnvironmental Science, Corp Jul 1987 - Nov 1988Performed wet chemistry and inorganic analyses, including Atomic Absorption.Prepared extractions for Gas Chromatography and Gas Chromatography/Mass Spectrometry analysis.Operated Gas Chromatograph for PCB and VOC analysis.
Francis Dumont Skills
Francis Dumont Education Details
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Chemistry
Frequently Asked Questions about Francis Dumont
What company does Francis Dumont work for?
Francis Dumont works for Atlantic Environmental Science
What is Francis Dumont's role at the current company?
Francis Dumont's current role is Environmental Scientist.
What is Francis Dumont's email address?
Francis Dumont's email address is fr****@****zer.com
What is Francis Dumont's direct phone number?
Francis Dumont's direct phone number is (212) 733*****
What schools did Francis Dumont attend?
Francis Dumont attended Central Connecticut State University.
What skills is Francis Dumont known for?
Francis Dumont has skills like Gmp, Validation, Pharmaceutical Industry, Strategic Sourcing, Sop, Technology Transfer, Clinical Development, Hplc, Cross Functional Team Leadership, Formulation, Drug Delivery, Fda.
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Francis Dumont's colleagues are Jack Dyer, Itjobsdotcom Inderas, Natan Reis Rubim Gonçalves, Don Bosseau, Danilo Farani, Samira Cristina De Souza Pinto, Adiana Clarke.
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