Experience

Mead Johnson Nijmegen

• Netherlands
• Food and Beverage Manufacturing
• 100 - 200 Employee

• Quality Control Manager

  • Feb 2022 - Present

  Manage all site laboratories with the scope of infant formula analytical testing to guarantee a sustainable adding value quality management system in compliance with EU and Asia regulatory agencies, including China GB requirement. With more then 130 method in scope the labs are divided in the following departments: • Chemical Full Label Claim Lab – Analysis of finished products, raw material, product base, etc using techniques such as IC, ICP, ICP-MS, UPLC-DAD, UPLC-MS-MS, GC, GC-MS, etc; • In process chemical lab – Analysis of in process markers including vitamins and minerals; • Physical and sensorial lab; • Microbiological Lab – Including EMP and finished product analysis; • Method validation – New method development, implementation, validation and method lifecycle overview; • Trial department – department responsible to project manage trials, new formulation implementation and change controls. Show less



Reckitt

• United Kingdom
• Manufacturing
• 700 & Above Employee

• • Oct 2019 - Feb 2022

  Manage all site laboratories with the scope of infant formula analytical testing to guarantee a sustainable adding value quality management system in compliance with EU and Asia regulatory agencies, including China GB requirement. With more then 130 method in scope the labs are divided in the following departments:• Chemical Full Label Claim Lab – Analysis of finished products, raw material, product base, etc using techniques such as IC, ICP, ICP-MS, UPLC-DAD, UPLC-MS-MS, GC, GC-MS, etc;• In process chemical lab – Analysis of in process markers including vitamins and minerals;• Physical and sensorial lab;• Microbiological Lab – Including EMP and finished product analysis;• Method validation – New method development, implementation, validation and method lifecycle overview;• Trial department – department responsible to project manage trials, new formulation implementation and change controls. Show less

• • Jun 2019 - Oct 2019

  Focused on implementing Best in Class quality release performance at the QC operation to establish RB as the World Leading Consumer Health Company and a benchmark to all our competitors.This role leads continuous improvement projects into the QC lab to implement KPIs, measurement tools, and facilitate process changes with the goal to improve productivity in a sustainable way guaranteeing compliance.

• • Apr 2019 - Oct 2019

  QC Lab manager Brazil and Argentina.

• • Jan 2017 - Apr 2019

  • Implementation of GMP data integrity and Quality Management System for local QC operation. • Develop Local method Validation systematics according to international guidelines, FDA legislation and local Legislation• Coordinate local lab operation including quality control activities and method validation. • Empower (Chromatographic data System) administrator – Responsible for system implementation, System Validation Documentation and implementing analytical process automation. • Trackwise (Change Control and Deviation management system) site super user. Responsible for local user’s qualification and system administration. Show less

• • Mar 2014 - Dec 2016

  • Head of the Quality Control Lab – Responsible for product release and implementation of a quality management system.• Empower 3 CDS Local Administrator - System Owner responsible for software implementation since project conception until computer system validation conclusion. • Site Validation Leader - Responsible for all process validation in Brazil manufacturing site e.g. Computer System, Manufacturing, Analytical Method and Water Supply.• Lead Auditor for Quality Assurance, Quality Control, Manufacturing Lines and Third Parties Manufactures. • Project manager – Including new quality Control Laboratory implementation. Show less



Novo Nordisk

• Denmark
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Quality Assurance Analyst

  • Aug 2011 - Mar 2014

  -Training Coordinator (Create, Update and Distribute SOPs) -Handle Non-Conformities (Document and Follow up) -Handle Change Requests (Document and Follow up) -Conduct Greenbelt (LEAN) Projects (Statistics analysis, mapping process, Establish KPIs, Improve process and procedures) -Importation process (release goods together with regulatory Agency) Cold Chain distribution and storage Validation (Write validation protocol, test parameters and statist analysis) -Training Coordinator (Create, Update and Distribute SOPs) -Handle Non-Conformities (Document and Follow up) -Handle Change Requests (Document and Follow up) -Conduct Greenbelt (LEAN) Projects (Statistics analysis, mapping process, Establish KPIs, Improve process and procedures) -Importation process (release goods together with regulatory Agency) Cold Chain distribution and storage Validation (Write validation protocol, test parameters and statist analysis)



Eli Lilly and Company

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Quality Control Analyst

  • Aug 2009 - Jul 2011

  Quality control analyst with a deep knowledge in HPLC (UV-Vis, Fluorescence and Light Scattering methods), GC (Mass Spectrometry and Electron Capture), IR and UV, understood by the American pharmacopoeia. Vast experiences with quality control methods validation and manufacture process validation. Quality control analyst with a deep knowledge in HPLC (UV-Vis, Fluorescence and Light Scattering methods), GC (Mass Spectrometry and Electron Capture), IR and UV, understood by the American pharmacopoeia. Vast experiences with quality control methods validation and manufacture process validation.



Laboratory of heterocyclic compounds - USP

• Chemical Researcher

  • Apr 2006 - Aug 2008

  Researcher at a innovation technological chemical laboratory, developing new chemical reactions methodologies. Submission of two scientific articles. Researcher at a innovation technological chemical laboratory, developing new chemical reactions methodologies. Submission of two scientific articles.