HAL Allergy Group

Supervisor QA Product Release – HAL Allergy Group – Leiden

Jobid=af134deea9d9 (0.0998)

Supervisor QA Product Release

Location Leiden (NL) | Hours 36-40 per week

 
This role is based in the Netherlands. Applicants must be eligible to work in the Netherlands.

Working at HAL Allergy means becoming part of one of Europe’s leading companies in the development, production, and distribution of allergen immunotherapies aimed at treating and preventing allergic diseases. Driven by enthusiastic and dedicated teams, we are currently seeking a QA Supervisor Product Release to join our QA Product Release team. In this role, you will oversee the batch review process for (investigational) medicinal products. You will collaborate closely with Production, QC, RA, QPs, and Tech Transfer to ensure the timely delivery of complete batch documentation, supporting on-time batch release. In addition, you will establish and maintain a culture of continuous quality improvement across the organization, enabling strong, quality-driven decision-making. Managing the daily operations of the QA Product Release team is also a key responsibility of this position.

Your tasks

  • Accountable for the performance of the QA Product Release department, you coordinate daily activities, set priorities, and ensure the team operates efficiently.

  • You drive and promote a strong QA culture, with a clear vision for continuous improvement across HAL Allergy.

  • You oversee and maintain the batch review process, including the management of related deviations.

  • You contribute to supplier and subcontractor audits when needed, assess the impact of changes on HAL batches, and support regulatory inspections (such as IGJ) as well as client audits. You also take part in internal audits.

    A key focus is ensuring timely closure of deviations—particularly when acting as investigation lead—and driving ongoing improvements.

  • You are an active member of deviation meetings and work closely with the Supervisor QA Systems to align on and address overarching QA topics.

  • You have

  • Academic degree (in Science or related field) or applicable experience.
  • Minimum of 5 years’ relevant experience in pharmaceutical industry, in a QA or RA role.
  • Experience with EU GMP guidelines. Knowledge of FDA is a plus.
  • Broad experience with quality related issues in aseptic production.
  • Experience with managing (small) teams. 
  • Fluent in English, both spoken and written; proficiency in Dutch is a strong advantage.
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