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Walloon BrabantOn siteHours negotiable<3months
As a QA Technician Formulation – Media Preparation (replacement contract), you are responsible for the quality assurance of GMP documentation, quality review, and fieldwork within a pharmaceutical company.
What you do
- Quality review of batch records and their timely closure on paper and in IT systems
- Ensuring proper adherence to procedures in the field
- Performing production audits, investigations in collaboration with production, and identifying risks that may impact the quality, efficacy, and safety of products (in collaboration with various support services)
- Performing EHS audits in the field
- Monitoring activities in Grade B zones
- First GMP contact for practices in aseptic zones
- Coordination of document flow between production and QA, verification of documentation present on site for proper application of procedures
- Adequate entries for tracking and release of batches (filling the QA GMP inspection plan)
- Regular checks on equipment in the production zone
- Support for GMP training
- Day shift schedule
What they ask
- Bachelor's degree in a scientific field (Chemistry, Biochemistry, Biology...) or an A2 (CESS) with more than 10 years of valuable experience
- Ideally, a first similar experience (pharmaceutical, laboratory, supply...)
- Demonstrates autonomy (while evaluating risky situations)
- Takes decisions and responsibilities
- Precise and rigorous
- Persevering
- Good team spirit and communicates easily
- Good critical and analytical mind
- Data Integrity
- Detail-Oriented
- Digital Fluency
- GxP Regulations
- Lean Management
- Pharmaceutical Regulatory Compliance
- Problem Solving
- Quality Assurance (QA)
- Risk Awareness
- Technical Writing
How to apply
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