Qualified Person (QP) & QA Lead — EU/GMP Compliance

Akkodis; Mont-Saint-Guibert; On-site; EUR 75,000 - 105,000; Full time

Job summary

Akkodis is seeking a qualified person (QP) in Belgium to lead Qualified Person activities within the QA/QP team. The role covers EU/Belgian regulatory compliance, GMP/GDP standards, and collaboration with CPSD, PR&D, and Regulatory Affairs to ensure quality and regulatory readiness.

The successful candidate will have 1+ year in a pharmaceutical environment and hold a Master’s in Pharmacy with QP status, and must be fluent in English.

Qualifications

• Minimum 1 year in pharmaceutical environment.
• Qualified Person status is required.
• Must speak and write fluent English.

Responsibilities

• Delegate Qualified Person tasks and related activities.
• QP involvement in batch release and deviations/change controls.
• QP certification for EU hub materials and QA approvals.
• Regulatory inspections participation and audit readiness.
• Final China Release/China distribution coordination as applicable.

Skills

GMP/GDP knowledge

Regulatory compliance

Quality assurance

English fluency

Education

Master’s in Pharmacy (Scientific)

Job description

Akkodis is seeking a qualified person (QP) in Belgium to lead Qualified Person activities within the QA/QP team. The role covers EU/Belgian regulatory compliance, GMP/GDP standards, and collaboration with CPSD, PR&D, and Regulatory Affairs to ensure quality and regulatory readiness.

The successful candidate will have 1+ year in a pharmaceutical environment and hold a Master’s in Pharmacy with QP status, and must be fluent in English.