Quentin Seisel

Analytical Capabilities Lead & Scientist at GSK

Brussels Metropolitan Area

About

PhD-Engineer / Therapeutics Developer / Problem Solver / Analytical Sciences Specialist / Let's connect!

Experience

  • Analytical Capabilities Lead - Scientist at GSK
    Mar 2022 - Present · 4 yrs 5 mos

    As a Technical R&D Scientist, I am developing and characterizing new vaccine prototypes. As the Analytical Capabilities Lead, I am the analytical expert and strategist of the department. _____Main tasks_____ - Implement and improve analytical tools used for characterization of vaccine formulations (proteins, nanoparticles, mRNA...) - Manage and take part in Drug Product Discovery projects of the department - Conceive, design, implement and interpret scientific and technical data in a Quality by Design framework - Coordinate and collaborate within a team of scientists and technicians - Provide guidance to other team members and act as the analytical specialist - Define the analytical strategy of the department - Optimize the laboratory organization through continuous improvement projects - Ensure application of high standards of ethics, good laboratory practices (GLP) and data integrity - Analyze, review and present key R&D data

  • Life Sciences consultant at ALTEN BELGIUM
    Oct 2018 - Mar 2022 · 3 yrs 6 mos

    As a Life Sciences consultant, I provide my chemistry/biotechnology experience in project management and problem solving for Pharma clients: - Zoetis (Louvain-la-Neuve) - Abbvie (Liège) - Baxter (Braine l'Alleud). _____Main areas of interest & expertise_____ - Analytical Method Development, Transfer and Validation - Lab Management and Optimization - Applied Research & Development - Optimization of Chemical Reactions and Processes (lab size/pilot size) - Drug Discovery & Preclinical Development - GLP/GMP Compliance _____Trainings______ - Lean Six Sigma Green Belt (October 2021) - Project Management (November 2021)

  • Analytical Development Scientist - Research Associate III at Baxter International Inc.
    Apr 2020 - Feb 2022 · 1 yr 11 mos

    As a Baxter Analytical R&D Scientist, I am an analytical expert developing novel analytical methods supporting new Nutrition products. I am also a SME (Subject Matter Expert) on UPLC-MS technology. _____Main tasks_____ - Developing & evaluating new analytical methods in the frame of R&D projects (UPLC-UV/MS, UPLC-CAD, IC-CD...) - Improving use and comprehension over the Waters QDa detector - Screening, evaluating and setting up new analytical technologies - Performing design of experiments (DoE) to support fast formulation prototyping - Analyzing, reviewing and presenting key analytical data - Troubleshooting complex technical issues - Training and supporting junior analysts - Managing R&D analytical projects (technical lead) - Maintaining a high standard of GxP compliance (quality, documentation) - Supporting other projects developed in the department (product, technical and software expertise)

  • QC Expert at ODYSSEA PHARMA
    Nov 2019 - Apr 2020 · 6 mos

    As the Odyssea Pharma QC lab Expert, I am leading the QC lab improvement projects as well as supervising lab daily activities and reviewing GMP documentation. _____Main tasks_____ - Leading and managing lab improvement projects (reagent organization, shortening of the QC lead time) - QC investigation, evaluation and optimization of physico-chemical analytical methods - Writing and reviewing lab documentation (batch records, laboratory investigation reports, etc.) - Organizing QC activities and managing QC technicians in their lab activities and planning - Implementation of Quality / EHS events and CAPA - Analytical Method optimization - Meeting high standards of GMP compliance

  • Analytical Development Specialist at Zoetis Inc.
    Nov 2018 - Sep 2019 · 11 mos

    In charge of Analytical Method Development, Optimization, Validation, Transfer and Troubleshooting projects for the QC laboratory and Production areas. Technical specialist for analytical instrument qualification (SoloVPE, NucleoCounter, UPLC-MS...) and investigations. _____Main tasks_____ - Analytical Method Development and Validation (UPLC-UV, UPLC-MS, particle sizing) - Analytical Instrument Qualification (IQ/OQ/PQ ; UPLC-MS, SoloVPE, NucleoCounter....) - Laboratory Investigation Support - Quality Documentation Writing (SOPs, qualification/transfer/validation protocols) - Project & People Management - Meeting high standards of GMP compliance