Description

Brahim – Brussels, Belgium

Bilingual (French/English) QA/QC professional with 7+ years of experience in the pharmaceutical industry. Strong expertise in Quality Assurance and Quality Control within GMP-regulated environments, with a proven ability to support compliance and quality improvement initiatives.

Adaptable and team-oriented, with excellent communication and stakeholder collaboration skills. Seeking to contribute to and grow within a QA or QC function.

Langues

Français
Bilingue ou natif
Néerlandais
Bilingue ou natif
Anglais
Capacité professionnelle complète
Arabe
Bilingue ou natif

Préférences en matière de lieu de travail

Accepte de travailler sur site

Brussels (jusqu’à 50 km)

E&BI Frameworks UCB
Lead E&BI frameworks
INDUSTRIE PHARMACEUTIQUE
août 2025 - octobre 2025 (2 mois)
Anderlecht, Belgique
Optimization and documentation of SOPs for various frameworks
Responsibilities:
• • Developed work methodologies for different frameworks.
• • Created SOPs to streamline routine tasks.
• • Optimized data through mapping creation.
• • Documented procedures for various frameworks.
• • Participated in meetings with the E&BI team
• • Technical Environment:VeeVault Source
Technical environment: SAP, LIMS, VeeVault Source, Discoverant, GMP,EU/US/JP Pharmacopoeia
UCB
Stability Reviewer
janvier 2024 - juillet 2025 (1 an et 6 mois)
Braine-l'Alleud, BW, Belgium
| Review of reports in the QC department for Stability Studies
Responsibilities:
• • Review of stability reports for chemical and biological products (ICH, annual and device reports)
• • Cross-checking Excel results against LIMS for creation of analytical trends
• • Verifying analytical results for accuracy and compliance with standards
• • Initiating OOT/OOS when results are non-compliant
• • Creating SOPs and guidelines to streamline document review
• • Defining conclusions based on stability data results/trends
• • Drawing conclusions on deviations, change controls, and lab investigations during stability studies
• • Completing and reviewing PQR/RM (Result Method) and SATSD
• • Weekly meetings with the stability team
• • Technical environment: SAP, LIMS, VeeVault Source, Discoverant, GMP, EU/US/JP Pharmacopoeia
Technical environment: SAP, LIMS, VeeVault Source, Discoverant, GMP, EU/US/JP Pharmacopoeia
PolyPeptide
Supervisor
août 2022 - janvier 2024 (1 an et 5 mois)
Braine-l'Alleud, Belgium
• • Performing and interpreting sample analyses
• • Reviewing chromatograms, Excel calculations, and providing critical feedback on results + modifying integrations per SOPs
• • Participating in interventions, planned maintenance, and qualification of analytical equipment (HPLC,GC,KF …)
• • Reporting deviations from analytical processes and participating in investigations
• • Determining root causes for initiated OOT/NCP/OOS
• • Reporting out-of-specification/out-of-trend results during supervision
• • Checked Certificates of Analysis (CoA) for accuracy.
• • Releasing APIs and supporting stability studies
• • Validated data to enable batch compliance.
• • Completed the Batch Record Release upon QC approval.
• • Technical environment: Chromeleon, LIMS, QUMAS, GMP
Technical environment: Chromeleon, LIMS, QUMAS, GMP