Qualified Person: Lead EU Product Release (Netherlands)

i-Pharm Consulting; Amsterdam; On-site; EUR 110,000 - 160,000; Full time

Benefits offered by this job

Relocation support

Job summary

i-Pharm Consulting partners with a leading pharmaceutical manufacturer to recruit a Qualified Person (QP) for the Netherlands. You will certify and release medicinal products, ensuring EU GMP compliance, Marketing Authorisations, and internal quality standards, collaborating across Quality, Manufacturing, Regulatory Affairs and Supply Chain.

Eligible QPs from Europe who can relocate to the Netherlands are invited to apply.

Qualifications

• Eligible to act as a Qualified Person in the Netherlands under EU Directive 2001/83/EC.
• Proven experience as a QP in GMP-regulated pharmaceutical manufacturing.
• Experience certifying and releasing medicinal products under a manufacturing licence.
• Strong understanding of EU GMP requirements, batch certification, quality systems, and regulatory compliance.
• Experience in sterile manufacturing, solid dose, generics, oncology, or similar environments is highly desirable.
• Ability to make quality-critical decisions with integrity; strong stakeholder management and communication skills.
• Professional proficiency in English.

Responsibilities

• Perform QP certification and batch release activities per EU GMP and applicable regulations.
• Certify and release medicinal products ensuring compliance with MA and quality standards.
• Review batch documentation, deviations, investigations, CAPAs, change controls, and quality records.
• Provide GMP and QP guidance to cross-functional teams.
• Support regulatory inspections, audits, and inspection readiness.
• Drive continuous improvement across quality systems and manufacturing operations.
• Support growth by enabling timely release of medicines to patients worldwide.

Skills

QP experience

EU GMP knowledge

Quality systems

Regulatory compliance

Stakeholder management

English proficiency

Education

EU Qualified Person status (QP)

Job description

i-Pharm Consulting partners with a leading pharmaceutical manufacturer to recruit a Qualified Person (QP) for the Netherlands. You will certify and release medicinal products, ensuring EU GMP compliance, Marketing Authorisations, and internal quality standards, collaborating across Quality, Manufacturing, Regulatory Affairs and Supply Chain.

Eligible QPs from Europe who can relocate to the Netherlands are invited to apply.