Tristan Fairbrother

Manager Analytical Services Center @W. R. Grace

Pasadena, MD, US
EMAILS
t••••••••@grace.com
MOBILE NUMBERS
+19•••••••73

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WORK HISTORY

Mar 2020 — Present

Manager Analytical Services Center @W. R. Grace

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Curtis Bay, MD, US

Leads the Analytical Service Center (ASC)- a center of excellence for both QC and R&D testing that operates 24/7/365. Successfully led projects to improve turnaround times for testing and drive down testing backlogs. Established a strong culture with respect to safety and continuous improvement across multiple labs. Driven best practices both within the ASC and across the wider Grace network. Worked globally to ensure successful transition to a new Laboratory Information Management System (LIMS)

EDUCATION

N/A

University of Brighton

BSc

SKILLS

Quality ControlGmpGlpChromatographyMethod DevelopmentLife SciencesSpectroscopyStandard Operating Procedure (Sop)Drug DevelopmentDrug DeliverySop DevelopmentAnalytical ChemistryTechnology TransferValidationInhalationHplcUv/Vis SpectroscopyChemistryGc-MsPharmaceutical IndustrySopFda5sLiquid Chromatography-Mass Spectrometry (Lc-Ms)Risk AssessmentRegulatory SubmissionsCorrective and Preventive Action (Capa)

ABOUT TRISTAN FAIRBROTHER

I am a Laboratory Manager with significant experience within the both the pharmaceutical and chemical industries. I have developed and led high performing departments in both a GMP and non-GMP environment, delivering on project milestones, applying operation excellence principles (lean, six sigma and 5S) to drive sustainable results. I am experienced in working across a matrix, making strategic decisions, setting goals and performance standards and delivering across multiple competing priorities. Over 15 years experience in inhalation product development (MDIs, DPIs, nasal sprays and nebulized solutions and suspensions) in both EU and US.In my career I have driven turnaround business performance across multiple laboratories – Quality Control Testing, Inhalation Development, Extractables and Leachables Testing and Microbiology. I have contributed to successful regulatory submissions including NDA and ANDA product submissions, CRLs and assembly of eCTDs. I have significant experience in selecting, installing and validating new analytical chemistry equipment into QC and product development laboratories. I am experienced at leading across a 24/7/365 working schedule and delivering flexibly to tight deadlines and budgets.

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