Regulatory Affairs Professional

vor 4 Wochen


Solothurn, Solothurn, Schweiz Ypsomed Vollzeit

Key Responsibilities

As a Regulatory Affairs Manager at Ypsomed, you will be responsible for supporting our rapidly developing Diabetes Care business, focusing on active and connected devices. Your tasks will include managing the development and implementation of regulatory strategies, preparing product submission documents for EU and US markets, and partnering with business stakeholders.

Requirements

  • University degree in Engineering, Natural/Medical Sciences, or equivalent experience
  • At least 4 years of professional experience in Regulatory Affairs with a focus on medical devices
  • 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)

Benefits

  • Work where and when you want (in Switzerland)
  • Up-to-date work environment with modern production, offices, and break areas
  • Pension fund with Ypsomed covering a portion of contributions
  • Flexibility with shiftwork, annual working hours, and part-time options
  • Free sport facilities and affordable gyms across Switzerland
  • Family-friendly financial contributions to childcare

About Ypsomed

Ypsomed is a successful, rapidly growing family-owned company with over 2,000 employees worldwide. We develop and produce injection and infusion systems for self-medication and enable people to self-treat chronic diseases with our market-leading products and solutions.



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