Experience

Eurogentec

• Belgium
• Biotechnology Research
• 200 - 300 Employee

• Senior Chemist

  • Dec 2020 - Present

  - Syntheses of special and/or complex oligonucleotides according to demand on time and respecting the required quality. - Ensure the manufacture of certain starting products by avoiding any stock shortage of these. • Provide the company with permanent leadership in production chemistry, through mastery of technologies and monitoring of new products. Analyze and propose the introduction of new reagents or new production processes. • Ensure the transmission and formalization of knowledge specific to the chemistry of RNA and other special/complex oligonucleotides. • Ensure the backup function of the Team Leader RNA. • Create and maintain team spirit and develop initiative within the production unit concerned. • Participate in some production meetings to discuss possible improvements, complaints, new products/processes/technologies. • Respond without delay to requests for cost prices for the establishment of commercial offers. • Inform the Production Manager objectively and as soon as possible of any major problem arising in connection with production. • Participate in the drafting of procedures Show less



Novasep

• France
• Chemical Manufacturing
• 300 - 400 Employee

• Process Characterization Scientist

  • Jan 2020 - Nov 2020

  Responsible for process characterization strategy and QbD activities (risk analysis, drafting of protocols and reports, design of experiments). Regular interaction with pour customers. Responsible for process characterization strategy and QbD activities (risk analysis, drafting of protocols and reports, design of experiments). Regular interaction with pour customers.



ALTEN Belgium

• Belgium
• IT Services and IT Consulting
• 400 - 500 Employee

• Consultant

  • Apr 2019 - Mar 2020



Baxter International Inc.

• United States
• Medical Equipment Manufacturing
• 700 & Above Employee

• QC Validation Scientist

  • Aug 2019 - Dec 2019

  The goal was to help Baxter in the validation/verification of analytical mathods of raw materials present in parenteral nutrition following the European pharmacopeia. - Writing verification/validation protocols following European pharmacopeia and spécifications from Baxter - Development and feasibility tests for analytical methods - Executing and reviewing of protocols and redaction of reports - Coordination and planning of the validation in collaboration with the QA and QC department - Reporting to the line manager/supervisor any deviations Show less



Novasep

• France
• Chemical Manufacturing
• 300 - 400 Employee

• Computerized system validation

  • Apr 2019 - Jul 2019

  Monitoring and reviewing of the existing documentation. Perform system configuration of 3 softwares: QuantStudio Design and Analysis v1.5.0, WinKQCL v5.3.3, Empower v3. Writing configuration procedures for 4 softwares: QuantStudio Design and Analysis v1.5.0, WinKQCL v5.3.3, Chromeleon v7.2.8, Empower v3 (AQ-B-FI-0181 version 00). Writing IQ/OQ protocols for 3 softwares: QuantStudio Design and Analysis v1.5.0, WinKQCL v5.3.3, Chromeleon v7.2.8. Test IQ/OQ of 4 softwares (QuantStudio Design and Analysis v1.5.0, WinKQCL v5.3.3, Chromeleon v7.2.8, ImageLab v5.2.1). Writing IQ/OQ report for 1 softwares: QuantStudio Design and Analysis v1.5.0. Coaching key user. Show less



aptaskil

• Belgium
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Coordinator in qualification/validation of biopharmaceutical processes and equipments

  • Dec 2018 - Mar 2019

  Good manufacturing practices (GMP, BPF), writing of Standard Operating Procedures (SOPs), people (dressing and behavior) qualification in controlled atmosphere area (ZAC), HVAC Qualification (IQ, OQ), bioreactor Qualification (IQ, OQ, PQ), autoclave Qualification (IQ, OQ, PQ), Quality Risk Management (FMEA, FMECA), Process performance qualification (stability, capability, intra- and inter-lot variability), Analytical method validation (HPLC), Cleaning validation, Computerized system validation Good manufacturing practices (GMP, BPF), writing of Standard Operating Procedures (SOPs), people (dressing and behavior) qualification in controlled atmosphere area (ZAC), HVAC Qualification (IQ, OQ), bioreactor Qualification (IQ, OQ, PQ), autoclave Qualification (IQ, OQ, PQ), Quality Risk Management (FMEA, FMECA), Process performance qualification (stability, capability, intra- and inter-lot variability), Analytical method validation (HPLC), Cleaning validation, Computerized system validation



Université de Namur

• Belgium
• Higher Education
• 700 & Above Employee

• PhD student researcher in organic chemistry

  • Oct 2014 - Dec 2018

  Laboratory of Bio-Organic Chemistry. FRIA financing. “Synthesis of unprecedented electron-deficient exo-glycals targeting the Mycobacterium tuberculosis cell wall’’. Organic chemistry (photocatalysis, multi-steps synthesis, carbohydrate, organometallic, pyrophosphate, inert and anhydrous atmospheres), project management, supervision of trainees, oral communication (poster and conference), 3 publications. Laboratory of Bio-Organic Chemistry. FRIA financing. “Synthesis of unprecedented electron-deficient exo-glycals targeting the Mycobacterium tuberculosis cell wall’’. Organic chemistry (photocatalysis, multi-steps synthesis, carbohydrate, organometallic, pyrophosphate, inert and anhydrous atmospheres), project management, supervision of trainees, oral communication (poster and conference), 3 publications.



Sanofi

• France
• Pharmaceutical Manufacturing
• 700 & Above Employee

• R&D Internship

  • Mar 2014 - Aug 2014

  TSU Infectious Disease. ‘’Synthesis and modulation of antibacterial agents’’. Organic chemistry (multi-steps synthesis, carbohydrate, continuous flow hydrogenation, chemistry of palladium). TSU Infectious Disease. ‘’Synthesis and modulation of antibacterial agents’’. Organic chemistry (multi-steps synthesis, carbohydrate, continuous flow hydrogenation, chemistry of palladium).