Sr. Associate Compliance – EU Regional Supply Chain | Pharma industry
Posted on October 16, 2025
Breda
English
Posted on October 16, 2025
About this role
As Sr. Associate Compliance within the EU Regional Supply Chain, you will ensure that the principles of Good Distribution Practice (GDP) and the Falsified Medicines Directive (FMD) are consistently applied across the network to maintain product quality and authenticity.
Key responsibilities include:
Key responsibilities include:
- Owning and managing temperature assessment (TE) records.
- Managing minor and major deviation records and leading root cause analysis sessions.
- Overseeing CAPA and CAPA EV records to ensure timely implementation.
- Managing missing product notifications and leading Event Review Team meetings when applicable.
- Supporting audits and inspections related to the European supply chain and affiliates.
- Contributing to product recall and mock recall exercises.
- Maintaining up-to-date records in Smartsheet for deviations, temperature excursions, and missing products.
- Acting as Subject Matter Expert (SME) for document management control.
- Supporting cross-functional improvement initiatives.
- Occasional travel may be required.
Requirements
- MBO or Bachelor’s degree in Life Sciences or related field (or equivalent experience).
- Minimum 2 years’ experience in GMP environments, with background in Quality Assurance or related functions.
- Knowledge of complaint management, deviations, and quality systems.
- Fluent in English; Dutch is an advantage.
- Strong analytical mindset, attention to detail, and ability to work both independently and collaboratively.
Salary
€4500-€4700 per month
The company
Our client is a leading global biotechnology company driven by a strong sense of purpose: to improve patients’ lives through innovative science and reliable supply. The Breda site plays a key role in the European supply chain network, where medicines are labeled, assembled, stored, and distributed to countries across the world. Every day, more than 1000 professionals from over 30 nationalities contribute to ensuring product quality, safety, and compliance at every stage of the proces
Application Procedure
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