Qualified Person - Netherlands

Overview

Join a dynamic life sciences organization where your expertise as a Qualified Person (QP) will directly impact product quality and compliance. This role offers a unique opportunity to grow within a collaborative environment, ensuring medicines meet rigorous standards. With on-site working in the Netherlands, you’ll be at the forefront of ensuring safe and effective healthcare solutions.

About our client

Our client is a reputable organization within the life sciences sector, dedicated to manufacturing and delivering high-quality pharmaceuticals. Their mission is to uphold the highest standards of safety and efficacy in their products, directly contributing to patient well-being. This role plays a vital part in maintaining compliance and quality assurance throughout their operations.

The opportunity (Role summary)

As a Qualified Person, you will oversee batch release and ensure regulatory compliance for pharmaceutical products. You’ll work closely with manufacturing, quality assurance, and regulatory teams to uphold stringent standards. The position is on-site in the Netherlands, offering an engaging environment for hands-on leadership in quality management and compliance.

Key responsibilities

• Lead batch release processes, ensuring products meet all quality and regulatory standards.
• Manage documentation and reporting for regulatory compliance and audits.
• Collaborate with cross-functional teams to resolve quality issues and improve manufacturing practices.
• Drive continuous improvement initiatives aligned with industry regulations.
• Maintain thorough knowledge of relevant legislation and guidelines affecting product releases.
• Ensure all processes adhere to Good Manufacturing Practices (GMP) and quality systems.

What you’ll bring

• Fully qualified as a pharmaceutical or biotech professional with current regulatory-approved QP certification.
• Extensive experience in the pharmaceutical industry, specifically in batch release or quality oversight.
• Strong knowledge of GMP, regulatory requirements, and pharmaceutical validation processes.
• Excellent communication skills, capable of collaborating across diverse teams.
• Proven track record of ensuring compliance and managing documentation for regulatory audits.
• Fluent in English, with the ability to work effectively in a fast-paced environment.

Compensation & benefits

This role offers a base salary range of £100,000–£110,000, depending on experience. It provides an excellent opportunity to advance your career in a reputable organization committed to quality and innovation.

Call to action

Apply now to join a team dedicated to advancing healthcare through strict quality standards and impactful work.

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