Brussels, Brussels Region, Belgium
- Spearhead product design changes, worldwide registrations, and launch activities for dialysis treatment and intensive care solutions. - Provide technical assessments for product modifications related to design, labeling, raw materials, manufacturing support, regulatory compliance, quality improvement, and new registrations in collaboration with senior scientists. - Coordinate and ensure follow-up on technical activities with key stakeholders, aligning with project commitments, quality procedures, and business needs. - Deliver timely technical support in response to authority inquiries, including FDA, TUV, and MOH audits. - Utilize project management methodologies such as Agile and Six Sigma to enhance project delivery and foster collaboration among team members.
- Led compendial awareness initiatives and follow-up for global operations at Baxter. - Ensured product, process, and method compliance with compendial regulations, including Ph.Eur, USP, JP, and ChP. - Collaborated closely with the European Pharmacopoeia, managing proactive interactions through the Belgian Pharmacopoeia and EDQM groups. - Evaluated the impact of proposed changes by testing new methods and assessing changes to criteria for equipment monographs.
Master Thesis « MODIFICATION OF METABOLIC AND MOLECULAR PATHWAYS K-RAS/B-RAF AND PI3K/PTEN IN RELATION TO THE MUTATIONAL STATUS OF EGFR AND HER2 EXPRESSION IN BREAST CANCER » Tools: CISH, FISH, PCR, PCR-RT
Traineeship required to become a professional pharmacist.
Traineeship in Analytical Chemistry and Galenic Preparations laboratories. Tools: IR, UV-Vis, NMR, HPLC, TLC