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Accomplished GMP quality manager, QA analytical lab manager, GMP production manager, formulations lead (CPIP) and project manager (PMP) in the pharmaceutical industry and medical device industry with over 20 years experience. Successfully managed a GMP production facility. Successfully managed projects (product development and initiatives). Successfully launched and lead a centralized formulations group (GLP) in Drug Safety Research & Development (Pfizer). Successfully served as a global formulations resource for DSRD. Managed, planned and coordinated DSRD formulation projects. Experience as a project formulator in preformulations and the development of oral formulations (solutions, suspensions, tablets, capsules and OPC’s).Specialties: GMP, GLP, GMP Production, Quality, Project Management, Preformulations, General Pharmaceutics Profiles, Toxicology Formulation Sciences
Invicro, A Konica Minolta Company
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Director Third Party Qa OversightInvicro, A Konica Minolta Company Aug 2021 - Present
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Director Quality Assurance (External Manufacturing)Invicro, A Konica Minolta Company Jul 2018 - Aug 2021
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Associate Director Chemistry Quality AssuranceMni (Division Of Invicro) Jun 2017 - Jul 2018
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Gmp Quality ManagerFoster Delivery Science Mar 2014 - Apr 2017
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Production Manager/Project EngineerFoster Delivery Science Jun 2013 - Mar 2014
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Formulation ScientistPfizer Drug Safety Research & Development Apr 2010 - Aug 2011Served as subject matter expert for scientific issues related to formulationsMentored and guided Formulation Laboratory ScientistsProvided input into the development of innovative and efficient strategies to support formulation development Prepared position papers and scientific reports for formulation initiativesParticipated in Practice Networks, Cross-line project teams, liaison roles, etc.Influenced the external environment through professional societies, planning symposia and cross industry collaborationsPrimary investigator for development of new formulation technologies and methodologies
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Formulations LeadPfizer Drug Safety Research & Development Jan 2000 - Apr 2010Managed all formulation functions and all formulation facilities (Pharmacy, Liquid Preparation Labs, Feed Blend manufacturing and Formulations Characterization Laboratory), supervised 9 formulation technicians and developed strategic direction for formulations group within GLP environment.Managed, planned and coordinated all formulation projects including resource allocation and scheduling for DSRD studiesMentored formulation technicians in developing and validating formulation methods, troubleshooting equipment, and solving complex technical problemsApproved and reviewed study plans, data files, reports and Out of Specification investigationsDeveloped working relationships with multidisciplinary groups and formulations staff to coordinate activities and balance project priorities, timelines and schedulesImplemented and evaluated new formulation technologies and formulation characterization techniques within DRSD-Groton and globallyDeveloped training programs for formulation functionsInteracted with Research Quality Assurance and the FDA during audits/inspectionsAccomplishments/Achievements:Established and lead global Formulations Practice NetworkSuccessfully established a dedicated formulations group within DSRDEstablished and implemented microscopy as a formulations characterization tool Validated and implemented bin blending technology as the standard feed blending processRepresented Groton DSRD on global Value Based Activities WorkstreamDrug Safety Excellence Award: 2002Scientific Leadership Development "Doubling Productivity" Award (2003) for establishing Formulations Characterization LaboratoryIndividual Performance Award (2007): Participation on Drug Safety training module team;
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Group LeadPfizer 2000 - 2010
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Group LeadPfizer 2000 - 2010
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Project FormulatorPfizer Pharmaceutical R&D 1995 - 2000Responsible for formulation development (project formulator)Designed and developed oral formulations for Discovery, toxicology, and Phase I clinical studies including suspension , solution, Oral Powder for Constitution (OPC), tablet and capsule formulationsDesigned and implemented experiments to improve oral bioavailabilityWrote clinical and toxicology formulation instructionsScreened Discovery Compounds for physicochemical propertiesPresented data to project teams
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Formulation Technician (Associate/Assistant Scientist And Laboratory Assistant)Pfizer Pharmaceutical Research And Development Jan 1985 - Jan 1995Developed and tested Toxicology, OPC and solid dosage formulationsDeveloped and implemented stability indicating assaysDesigned and developed new laboratory techniquesInstructed laboratory scientists in new techniques Presented data in staff reports, formulation instructions & at staff meetings
Troy Appleton Skills
Troy Appleton Education Details
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University Of New HavenMba -
The College Of WoosterChemistry -
Sewickley Academy -
Cpip -
Pmp (Pmi)
Frequently Asked Questions about Troy Appleton
What company does Troy Appleton work for?
Troy Appleton works for Invicro, A Konica Minolta Company
What is Troy Appleton's role at the current company?
Troy Appleton's current role is Director at Invicro, A Konica Minolta Company.
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What schools did Troy Appleton attend?
Troy Appleton attended University Of New Haven, The College Of Wooster, Sewickley Academy, Cpip, Pmp (Pmi).
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Troy Appleton has interest in Football, Exercise, Sweepstakes, Home Improvement, Shooting, Reading, Sports, Watching Basketball, Golf, Home Decoration.
What skills is Troy Appleton known for?
Troy Appleton has skills like Pharmaceutical Industry, Formulation, Drug Development, Gmp, Pharmaceutics, Drug Discovery, Clinical Development, Fda, Glp, Pmp, Chemistry, Toxicology.
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