Skip to content

1 vacancy

Qualified Person jobs

Qualified Person jobs at pharma, biotech and CDMO sites, technically screened by a GMP consultant. There is currently 1 open role across the EU. Qualified Persons, Deputy QPs and QP-track QA Managers for batch certification under Annex 16 at manufacturing and import sites across the European Union. Every vacancy states the client type, contract form, salary band and whether Dutch is required. Not seeing the right role? Register and we will call you when one opens; most Qualified Person roles in this market are never advertised.

(Example vacancies. These show how a role is presented; they are not live searches.)

  • QPPermanent

    Qualified Person (Deputy)

    Generics manufacturer, Utrecht region

    Named Deputy QP on a multi-product oral solid dose licence; Annex 16 certification for 40+ SKUs.

    €95–115k
    Utrecht

Consultant for this discipline

Gregory Sivo

Founder · Practising GMP quality professional

  • · Founder, Truex Consultancy: GMP and GDP compliance
  • · 10+ years in regulated pharmaceutical quality
  • · Personally conducts every technical conversation

Frequently asked questions

Who can become a Qualified Person?

Anyone who meets the education and experience requirements of Article 49 of Directive 2001/83/EC, as implemented in the member state where the licence is held. The precise route differs per country; we check eligibility before any introduction.

Is a QP qualification recognised across the EU?

Eligibility is assessed per member state under the same Directive, but national implementations differ in the documentation required. A QP moving countries usually needs to be re-registered on the new licence.

How confidential is a QP search?

Very. The pool is small and most QP roles are not advertised. We approach eligible QPs directly, and the first conversation is with a consultant who knows the work from the inside.