| Location | Mol, Belgium |
|---|---|
| Business Sector | Biotechnology |
| Contact email | |
| Job ref | 26490 |
| Published | 6 days ago |
As a QA Associate, you will support day-to-day quality assurance activities within a highly regulated pharmaceutical manufacturing environment. You will be involved in batch record review, handling deviations and CAPAs, release of incoming raw materials, and supporting supplier-related quality activities in line with GMP requirements. Working closely with Production, QC, and other internal stakeholders, you will help ensure product quality, compliance, and inspection readiness. This is a hands-on QA role in a fast-evolving, quality-driven organization contributing to innovative cancer therapies.
Location: Mol, Belgium
Working model: On-site / Hybrid
Start date: ASAP
Bachelor’s degree in Chemistry, Engineering, Life Sciences, or a related field
Minimum 3 years of experience in a Quality Assurance role, preferably within pharmaceutical or manufacturing environments
Solid understanding of GMP and quality assurance principles
Experience with batch record review, deviations, and CAPA activities
Familiarity with supplier-related quality activities
Willingness to work in a controlled (nuclear/pharmaceutical) environment with strict safety and regulatory protocols
Strong written and verbal communication skills
Excellent attention to detail and organizational skills
Proficiency in Microsoft Office
Experience working in a GMP/GDP-regulated environment
Exposure to supplier qualification or supplier management activities
Familiarity with regulatory requirements and quality standards (e.g. cGMP, ISO)
Experience supporting continuous improvement initiatives, training, or change activities
Ability to work effectively in a fast-changing environment
Interested? Apply below or reach out directly at k.vongeusau@panda-int.com.