Publié: 01 juin 2024
Solothurn
80% – 100%
Durée indéterminée
Ypsomed AG
Emplois trouvés sur le web
In the Business Area Diabetes Care in Solothurn we are looking for an experienced skilled personality as a
Location: Solothurn | Hybrid
Help us bring to market state-of-the-art medical technology solutions by optimizing processes and ensuring quality through your structured approach.
[Focus of this position is supporting our rapidly developing Diabetes Care (active and connected devices), Manage the development and implementation of regulatory strategies, Support and prepare product submission documents with main focus on EU and US, Partner with business stakeholders on different levels, Communication and correspondence with authorities, Cooperation in QMS ISO 13485 and 21 CFR 820 audits, General QM tasks (Creation of Q-documents, trainings etc.)]
[University degree preferably in Engineering or Natural/Medical Sciences or equivalent experience, At least 4 years of professional experience in Regulatory Affairs with focus medical device, Expertise in Active Medical Devices related regulations and guidance documents in EU and US, Excellent organizational and people skills, Very good English knowledge (Level C2 or MT)]
More than 2,000 employees worldwide develop and produce injection and infusion systems for self-medication with the Ypsomed Group. We are a successful, rapidly growing, family-owned company headquartered in Burgdorf (CH) with various production sites and subsidiaries around the world. With our market-leading products and solutions, we enable people all over the globe to self-treatment. Despite chronic diseases such as diabetes, obesity, or certain types of cancer, they are provided with the greatest possible quality of life.
Alain Rusconi
Human Resources Expert Recruiting
+41 (0) 34 424 28 64
Solothurn
Solothurn