Join a leading global biopharmaceutical company in Haarlem, where you'll play a vital role in Quality Release. Contribute to the release activities, optimize internal processes, and enhance efficiency and transparency. Engage in data checking, identify bottlenecks, and drive quality improvements. Support process integration and standardization through project-based activities. See how you can contribute to our success by reading further.

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Hays

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Your new company
Our client is a leading company in global biopharmaceuticals with a diverse portfolio of prescription medicines, oncology, vaccines and animal health products. With 69,000 employees operating in more than 140 countries, they offer state-of-the-art laboratories, plants and offices that are designed to inspire their employees as they learn, develop and grow.
In Haarlem, our client distributes 2,500 different (packaging of) medicines to more than 140 countries. The site is known as the flexible packaging location in Europe, as they can quickly switch between different packaging and medicines. From jars to blisters and from syringes to powders. All provided with the right packaging and leaflet in the right language. Furthermore, MECTIZAN® is produced at the site, a medicine for river blindness and elephant disease. This medicine has been made available free of charge to the WHO for 30 years in the fight against these diseases.

Your new role
In this position within Quality Release, you will contribute to the release activities and optimise our internal processes. You strengthen our impact on people and health by working at the intersection of quality, compliance and operations. You make a concrete contribution to our efficiency, transparency and result-orientation.
What will you do?

Data checking: Perform thorough checks on batch documentation to ensure data accuracy and completeness.Identify bottlenecks: Identify opportunities and bottlenecks in collaboration between departments and improve internal work processes (SOPs) based on conversations with specialists.Quality improvements: Contribute to the quality of the CoE Quality and the IPTs byInitiating and monitoring quality improvements.Project-based activities: Support the creation, coordination and execution of timelines and schedules for process integration and standardisation. Convert 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.

What you'll need to succeed
The most suitable candidate will have HBO level of education or relevant work experience in Life Sciences. GMP experience is required and having an analytical and structured approach to your work is essential. Mastery of the Dutch and English language (both written and spoken) is a hard requirement for this role, along with knowledge of laws and regulations within the (bio)pharmaceutical sector.

What you'll get in return
Hays Detachering | This is a project that will start with a contract for 12 months through Hays. Extension to stay within the department is anticipated. In this position, you will get a competitive salary and your travel expenses are covered.

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.
#1049049

Salaris

Competitive Salary + Travel Expenses

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