Join a global healthcare leader at a pivotal site for pharmaceutical production and packaging. Contribute to impactful release activities and optimize processes at the intersection of quality, compliance, and operations. Enhance internal workflows, initiate quality improvements, and transform data into insightful dashboards. Be part of a team that values innovation, offering an opportunity to implement a cutting-edge training environment and track performance with data-driven insights. See what awaits you in this role by reading on.

Over het bedrijf

SIRE Life Sciences

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The Company
Our client is a global healthcare company committed to improving lives through the development of innovative medicines and vaccines. The Haarlem site is a key hub for the production and packaging of high-quality pharmaceutical products. As part of a worldwide network, the company upholds the highest standards in quality, safety, and compliance.

The Role
In this position, you contribute to release activities and help optimize internal processes. You strengthen our impact on people and health by working at the intersection of quality, compliance, and operations.

Responsibilities

Conduct thorough reviews of batch documentation to ensure data accuracy and completeness.
Spot opportunities and obstacles in cross-department collaboration and improve internal workflows (SOPs) based on discussions with specialists.
Contribute to the quality of the CoE Quality and IPTs by initiating and monitoring quality improvement initiatives
Support the creation, coordination, and execution of timelines for process integration and standardization. Transform Haarlem Batch Release data into digital dashboards and develop data-driven impact measurements (KPI performance tracking). Implement an innovative training environment (GATE) and evaluate data, guidelines, and procedures.

Requirements

HBO/WO (Bachelor’s/Master’s) working and thinking level, preferably with a data-driven background, health sciences, or a related field.
Passionate about data research, highly motivated, and able to work independently to review or create high-standard documentation.
Strong analytical skills, structured in your approach, and capable of simplifying complex problems into clear, practical solutions.
Good communication skills in both Dutch and English, enabling effective collaboration with various stakeholders.
Familiarity with laws and regulations in the (bio)pharmaceutical sector is a plus for navigating our quality landscape.

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