Responsibilities
Taking care of the quality management software as system administrator.
* Support and train users.
* Improve and update processes including relevant SOPs and documents.
* Harmonize processes.
* Lead projects.
* Implement additional modules and functionalities within the quality management software.
Qualifications
* Background in analytical chemistry, biochemistry, or life science.
* Experience in the analytical‑pharmaceutical environment, preferably in QA.
* Skills to solve problems and build good relationships with stakeholders.
* Good interpersonal skills and teamwork spirit.
* Ability to collaborate in a dynamic, cross‑functional matrix environment.
* Ability to lead projects between sites and work independently.
* Broad knowledge and proven experience of the regulatory framework in the GMP environment (ICH, FDA, USP, Ph.).
* Solid background in data integrity and computerized systems risk assessment and project support.
* Experience as system administrator or deeper IT knowledge is an asset.
* Fluency in English and German is a plus and required.
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