Regulatory Affairs Specialist

☞ CareerAddict

View: 214

Update day: 21-03-2024

Location: Solothurn Solothurn SO

Category: Legal / Contracts

Industry: Legal Services

Position: Entry level

Job type: Full-time

Loading ...

Job content

We are currently looking on behalf of one of our important clients for a Regulatory Affairs Specialist. The role is a permanent position based in Solothurn Canton.

Your Role
  • Support the implementation of business strategies.
  • Act as an interface with internal & external stakeholders, FDA & other regulatory authorities.
  • Support & coordinate complex Regulatory Affairs projects.
  • Prepare effective regulatory strategies in coordination with internal & external stakeholders.
  • Drive the preparation of product submissions.
  • Support development projects with a focus on regulatory aspects.
  • Evaluate change requests.
  • Review quality agreements with customers on regulatory aspects.
Your Skills
  • At least 3 years of professional experience in Regulatory Affairs, including experience with a focus on Medical Devices.
  • Good experience in the areas of Active Medical Devices, Software as a Medical Device, Digital Health & US Submissions.
Your Profile
  • Completed University Degree in Natural/Medical Sciences/Engineering or equivalent training.
  • Highly organized & efficient.
  • Skilled in communicating effectively with different stakeholders & on different levels.
  • Fluent in English (spoken & written) & a good command of German (At least B1/B2 Level).
If you wish to apply, please send us your resume in Word or PDF format.
Loading ...
Loading ...

Deadline: 05-05-2024

Click to apply for free candidate

Apply

Report job
Loading ...
Loading ...

SIMILAR JOBS

Loading ...
Loading ...