Deputy Qualified Person (QP)

About the Company

We are supporting a leading European pharmaceutical group with a strong heritage in research, development, and manufacturing of both sterile and non-sterile products. The company operates under the highest quality and compliance standards and continues expanding its international footprint.

As part of its growth strategy, the company is seeking to appoint a Deputy Qualified Person (QP) to join the Quality team at one of its key manufacturing sites.

Role Overview

The Deputy QP will act as a key member of the Quality Assurance department, supporting the Qualified Person in ensuring that all products released to market comply with EU GMP and regulatory requirements. This position offers the opportunity to develop within a highly reputable organization and to eventually assume full QP responsibilities.

Key Responsibilities

• Support the Qualified Person in the batch certification and release process according to Directive 2001 / 83 / EC and EU GMP Part I, Chapter 1.
• Review manufacturing and quality documentation, including deviations, CAPAs, and change controls.
• Participate in internal and external audits, ensuring ongoing GMP compliance.
• Contribute to continuous improvement initiatives within the QA and manufacturing teams.
• Provide technical and regulatory support for product quality and validation activities.
• Collaborate cross-functionally with Production, QC, Regulatory Affairs, and Supply Chain.
• Act as a back-up QP when delegated and authorized.

Requirements

What’s Offered