Qualified Person (QP) – Hybrid, Full‑time

About the role

Join QbD Group as a Qualified Person (QP) and gain hands‑on experience across pharmaceutical, biotech and medical‑device projects. You will work in a hybrid setting, supporting batch release, GMP documentation and quality‑system activities while being mentored by seasoned professionals.

Key responsibilities

• Support batch review and release activities in compliance with EU GMP.
• Interpret and apply GMP documentation, contributing to QP responsibilities.
• Work on deviations, CAPAs, change controls and drive continuous improvements.
• Participate in audits and inspections, preparing documentation and liaising with authorities.
• Collaborate with stakeholders across diverse client environments, including sterile manufacturing sites.

Required profile

• Master’s degree in Pharmaceutical Sciences, Industrial Pharmacy or a related scientific field.
• Eligibility or strong ambition to obtain Qualified Person certification.
• Initial hands‑on GMP experience (internship or first job).
• Fluency in Dutch and English.

Required skills

• GMP knowledge
• Batch review and release
• Sterile manufacturing processes
• Deviation management
• CAPA handling
• Change control procedures
• Audit and inspection support

What we offer

• Exposure to multiple sectors – pharma, biotech, MedTech.
• Mentoring and professional development within a fast‑growing international team.
• Hybrid work model with a stable employer.