Qualified Person (QP) - 2001/83/EC

The organisation

The client I have partnered with is a part of a global pharmaceutical organisation, experiencing such growth that they are now at a point where they need a full time permanent Qualified Person (QP). They are a global leader for a specific product within their field, making their product not only reputable but also very lucrative.

They are situation around the Breda/ Tilburg area in Noord-Brabant of the Netherlands, situated on the Dutch/ Belgian border.

Their need

A Qualified Person (QP) is the main attraction for them, to perform:

• Batch release for their product according to Directive 2001/83/EC
• Great experience end exposure within GMP
• Communicate with competent authorities
• Supervise general conditions of hygiene of the premises
• Fill in for Site Quality Head if they are absent
• Collaborate with site manager, QC and production staff

You will be performing your duties mainly as a QP but also as QA Manager, on site full time for a permanent post. 

Your background and experiences:

You will have:

• Minimum of 2 years as a QP
• Eligibility to be a QP in the Netherlands
• Fluent in Dutch and English, both written and verbal
• Adhered to GMP standards

YOu will be supporting the site quality head in maintaining an effective implementation, monitoring and maintenance of a GMP-compliant quality system, so your experience here has to be essential. Being based on site full time is also essential, as you will be the main QP so you will be required as per Article 48 Directive 2001/83/EC.

To apply:

Send me across your CV and call me on +44 1293 776644 or click the apply button. Your application will come to me directly and we can discuss your current situation, motivations and if this position is the right move for you.