Troy Appleton

Director Third Party Qa Oversight @Invicro

Groton, CT, US

EMAILS

t••••••••@invicro.com

MOBILE NUMBERS

+18•••••••45

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WORK HISTORY

Aug 2021 — Present

Director Third Party Qa Oversight @Invicro

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New Haven, CT, US

EDUCATION

N/A

University of New Haven

MBA

N/A

The College of Wooster

Bachelor's degree, Chemistry

SKILLS

Pharmaceutical IndustrySopFdaLife SciencesU.s. Food and Drug Administration (Fda)PharmaceuticsDrug DiscoveryR&DGood Laboratory Practice (Glp)Regulatory SubmissionsPmpBiotechnologyChemistryResearch and Development (R&D)ValidationCROIndTechnology TransferClinical DevelopmentFormulationQuality ManagementOncologyAssay DevelopmentLifesciencesProtein ChemistryProject ManagementLaboratoryDrug DevelopmentBiopharmaceuticalsToxicologyStandard Operating Procedure (Sop)GlpGmpQuality Assurance

ABOUT TROY APPLETON

Accomplished GMP quality director, 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

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