Regulatory Medical Jobs in Lausanne

Lausanne, Waadt, Switzerland

Novostia is a clinical stage company founded in April 2017, in Switzerland, that is developing a breakthrough heart valve prosthesis offering superior benefits and quality of life to young adults and elderly...

von: jobleads.de - Vor mehr als 30 Tagen

Debiopharm - Lausanne, VD

The use of external staffing agencies or recruiters requires prior approval from our Human Resources Department. The Human Resources Department at Debiopharm requests external staffing agencies or recruiters...

von: workable.com - Vor mehr als 30 Tagen

Lausanne, Waadt, Switzerland

In depth experience with design, conduct, analysis, interpretation and reporting of randomized clinical trials (RCTs) and adaptive designs for rare disease, ideally in the regulated environment of “orphan...

von: jobleads.de - Vor mehr als 30 Tagen

Vevey, Waadt, Switzerland

Lead and advance digital footprint of Nestle Nutrition Institute (NNI) and the Wyeth Nutrition Science Center (WNSC) with global healthcare audiences through information, communication, and education initiatives...

von: jobleads.de - Vor mehr als 30 Tagen

RegenLab SA - Le Mont-sur-Lausanne

If you are passionate about regulatory affairs and thrive in a fast-paced and dynamic environment, we invite you to join our team and be part of our mission to improve healthcare worldwide. Apply now by...

von: jobscout24.ch - Vor 24 Tagen

Aubonne, Waadt, Switzerland

Take part in internal/external audits and inspections, ensuring that company procedures, processes, and documentation meet Quality Management System, ISO 13485, and other applicable regulations' requirements...

von: jobleads.de - Vor mehr als 30 Tagen

Dentsply Sirona - Ballaigues

3-5 years’ experience within international multi-disciplinary R&D or QA/RA organizations in the area of medical device design control and regulations (21 CFR part 820, 93/42/EC Directive, 2017/745 EU Regulation...

von: jobscout24.ch - Vor 15 Tagen

Dentsply Sirona - Ballaigues

Very good knowledge of European Regulatory rules (MDR) and US (21 CRF) concerning medical devices, FDA Clinical input during product development, definition of clinically relevant product performance parameters...

von: jobscout24.ch - Vor 15 Tagen