L'offre
Your responsibilities
- Quality Review of Validation Documentation, Change Records and Procedures
- Regulatory Impact assessments
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Coordination of Regulatory Submissions and Responses- Support in Quality Management Systems (Validation, QRM, Change Management, Regulatory Systems…)
Profil recherché
Your skillset
- Minimum Master's degree in science
- Minimum 1 year of experience within the pharmaceutical industry
- Interest in validation, quality and government agencies and documents
- Experience in validation and now wants to be on the other side (QA) or has already performed a similar job as QPA
- Scientific background and strong analytical skills
- Knowledge of medication legislation and organizations (FDA, EMA)
- Good writing and communication skills
- Dynamic, flexible, dealing with high work pressure
- Take initiative and be able to work independently
- Minimum of full professional proficiency in Dutch and English
It is essential to us that each new colleague fits the corporate culture. We believe in an open and collaborative workplace where transparency is paramount. We encourage creativity, challenge accepted best practices and focus on internal knowledge. But most of all, we hold integrity and honesty in high regard. To us, mutual respect is the key to long-term growth. We focus on total client satisfaction in everything we do.
Our offer includes a highly competitive remuneration program, including multiple supplementary benefits. You will have the chance to shape your own career and to further grow your professional expertise. Apply today and become part of an ambitious team of experts with a focus on people, quality and knowledge.
