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.

Languages

French
Native or bilingual
Dutch
Native or bilingual
English
Fluent
Arabic
Native or bilingual

Workplace preferences

Can work on-site

Brussels (up to 50km)

E&BI Frameworks UCB
Lead E&BI frameworks
PHARMACEUTICALS INDUSTRY
August 2025 - October 2025 (2 months)
Anderlecht, Belgium
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
January 2024 - July 2025 (1 year and 6 months)
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
August 2022 - January 2024 (1 year and 5 months)
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