QA Associate

QA Associate – Nuclear & Pharmaceutical Manufacturing

As a QA Associate, you will be responsible for ensuring product and process quality in a highly regulated pharmaceutical manufacturing environment. You will handle deviations, investigations, complaints, batch documentation review, and CAPA activities in line with GMP requirements. Working closely with Manufacturing, QC, Engineering, and external partners, you will help maintain inspection readiness and regulatory compliance. This is a hands-on role in a fast-evolving, quality-driven organization supporting innovative cancer therapies.
 

Practicalities

• Location: Mol, Belgium

• Working model: On-site / Hybrid

• Start date: ASAP
   

Must-haves

• Bachelor’s degree in Life Sciences, Chemistry, Engineering, or a related field

• Minimum 5 years of experience in a QA role within the pharmaceutical industry

• Strong understanding of GMP, regulatory requirements, and quality systems

• Experience with deviations, investigations, complaints, and CAPA management

• Experience reviewing batch manufacturing, packaging, and QC documentation

• Willingness to work in a nuclear and pharmaceutical controlled environment

• Strong written and verbal communication skills

• Excellent attention to detail and organizational skills

• Proficiency in Microsoft Office
   

Nice-to-haves

• Experience supporting internal, regulatory, or customer audits and inspections

• Knowledge of risk management tools (e.g. FMEA)

• Experience with supplier qualification and supplier audits

• Experience supporting GMP or quality-related training

• Ability to work in a fast-changing environment
   

Interested? Apply below or reach out directly at k.vongeusau@panda-int.com.