Stellenbeschreibung
We are seeking a detail-oriented and experienced Regulatory Affairs Specialist to support our client’s regulatory activities in Basel. In this role, you will be responsible for ensuring compliance with relevant health authority regulations and supporting product registrations and lifecycle management. This is a great opportunity for someone passionate about regulatory processes in the pharmaceutical or medical device industry.
What You’ll Do
* Prepare and submit regulatory documents for product registrations and renewals
* Ensure compliance with local and international regulatory requirements (e.g., Swissmedic, EMA, FDA)
* Collaborate with cross-functional teams including quality, R&D, and manufacturing
* Monitor regulatory changes and assess their impact on existing products
* Support audits and inspections by health authorities
What You Bring
* Degree in life sciences, pharmacy, or a related field
* At least 2–4 years of experience in regulatory affairs, ideally in a regulated industry
* Strong knowledge of Swiss and international regulatory frameworks
* Attention to detail and the ability to manage documentation efficiently
* Fluency in German is mandatory, English is also required
What We Offer
* A stable and impactful role in a highly regulated industry
* Competitive compensation and benefits package
* Opportunities for professional development and growth
* A collaborative and experienced regulatory team in Basel
Die DEKRA Arbeit Gruppe ist Teil der DEKRA SE und seit Jahren einer der am stärksten wachsenden Personaldienstleister in ganz Europa. In der Schweiz und im Fürstentum Liechtenstein profitieren Unternehmen und Bewerber dank unseren erfolgreichen Niederlassungen von umfassenden vermittlungsorientierten Personaldienstleistungen. Mit uns bauen Sie Ihr Erfolgsmodell immer weiter aus. Bewerben Sie sich jetzt und werden Sie Teil des DEKRA Arbeit Gruppe-Teams! Wir freuen uns auf Ihre Bewerbung.