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Regulatory affairs officer

IQVIA Holdings Inc.

Zaventem, Belgium

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

You will be the support of the regulatory activities within the organization:
- Preparation, submission and follow-up of registration dossiers for medicinal products in Benelux (new applications, variations and renewals)
- Maintenance of a database for registered technical details
- Adaptation and verification of SPC, PIL and packaging materials
- Implementation of labelling of marketed products following approval
- Support for pharmacovigilance activities
- Assistance in SOP writing
- Follow-up of legislation
- Development of expertise in specific areas such as nutrients
Profile: 
- Pharmacist or Master degree in pharmaceutical sciences
- Experience in regulatory affairs is an asset
- Knowledge of regulations for pharmaceutical products
- Accurate and efficient
- Flexible, dynamic, organized, team player
- Very good knowledge of Dutch, French and English
You will report to the Regulatory Affairs Director

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

Job posted: 2020-07-03

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