Qualified Person (QP)/ Responsible Person (RP), Netherlands

Qualified Person (QP) / Responsible Person (RP), Netherlands

Location: Home-based – anywhere in the Netherlands, with national travel as required.

Talentmark is partnering with an international healthcare organisation to recruit an experienced Qualified Person (QP) / Responsible Person (RP) to lead GMP and GDP compliance, ensuring the quality, safety and regulatory compliance of medicinal products.

This is a key position combining pharmaceutical quality leadership with country-specific regulatory research to support market access, licensing and submissions for the Marketing Authorisation Holder.

Key Responsibilities:
Certify and release medicinal product batches in accordance with GMP requirements.
Be key authority for GMP and GDP compliance and oversee the Quality Management System.
Manage supplier qualification, Quality Agreements and contract manufacturing relationships.
Oversee audits, inspections, recalls, complaints, deviations and CAPAs.
Ensure compliant importation, storage, transportation and distribution of medicinal products.
Liaise with regulatory authorities and support inspections.
Conduct Dutch country-specific regulatory research to support market access, licensing and regulatory submissions.Requirements:
MSc or equivalent qualification in Pharmacy, Chemistry, Biology or a relevant Life Sciences discipline.
Eligible to act as a Qualified Person within the EU.
Native Dutch speaker with strong knowledge of the local regulatory environment.
Extensive GMP and GDP knowledge and experience in pharmaceutical quality.
Experience with regulatory authorities, inspections and quality management systems.
Understanding of market access, licensing and regulatory submissions.
Willingness to travel throughout the Netherlands as required.The Opportunity
Home-based in Netherlands, but requirement to travel throughout Netherlands as and when required due to the nature of role.
Combined QP and RP responsibilities within an international healthcare environment.
Opportunity to influence quality, compliance and regulatory market access.
A meaningful role supporting patient safety and healthcare outcomes.
Apply:

It is essential that applicants hold entitlement to work in the Netherlands. Please quote job reference 71656 in all correspondence
Only candidates based in UK and eligible to work in UK are allowed