Global QA/RA Director M/V/X

Description de la fonction

Our client is a global leader in clinical and commercial packaging solutions for the pharmaceutical and biotech industry. With state-of-the-art facilities and a strong reputation for quality, innovation, and compliance, the company supports customers throughout the full product lifecycle-from design to delivery.

To strengthen its global Quality organization, we are recruiting a: Global QA/RA Director
As Global QA/RA Director, you will: Report directly to the SVP Global Quality (dotted line to the SVP & Managing Director Clinical & Europe). Be an active member of both the European Commercial Management Team and the Global Clinical Leadership Team. Lead and coach QA Heads and sub-functions across four international sites. Define, harmonize, and implement global quality policies, standards and procedures, aligned with cGMP, internal requirements, and client expectations. Champion a solid Quality Culture across clinical, packaging and operational activities. Collaborate cross-functionally with Technical, Operations, Engineering, Business Development and Supply Chain. Oversee the Pharmaceutical Quality System (PQS) and drive continuous improvement. Optimize quality systems, clarify roles and structure of local QA teams. Supervise batch record review, validation activities (equipment, cleaning, CSV), and key compliance processes. Lead audits (client, supplier, agency) and manage regulatory filings as needed. Handle customer escalations and lead global management review processes. Stay up to date with regulatory trends and represent the company toward health authorities, clients, and suppliers. Manage the quality budget and contribute to strategic planning at global level. Travel across Europe and th e US when required.

Profil

Master's degree minimum, ideally in Pharmacy, Life Sciences or related field. Additional certifications in QA/RA or GxP are a strong asset. 15+ years experience in senior QA/RA roles in the pharmaceutical sector. Proven track record managing international, multi-site quality teams. Deep knowledge of GxP, quality systems, validation and regulatory requirements. Fluent in English (Dutch is an asset). Strategic mindset with strong operational leadership and hands-on spirit. Excellent communication, influencing and change management skills. Willingness to travel internationally.

Compétences linguistiques

• Néérlandais (atout)

  • Comprendre : Expérimenté - (C1)
  • Écrire : Expérimenté - (C1)
  • Lire : Expérimenté - (C1)
  • Parler : Expérimenté - (C1)

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