Regulatory Affairs Specialist

Posted 10 Vendredi juin
Type d'offre Temporaire

Job description

Trust in our expertise - we successfully bring clients and candidates together!

Job Description: Regulatory Affairs Specialist (m/f/d) - 100%

For our client, a pharma company in Schaffhausen specialized in ophthalmology, we are looking for a highly motivated person to join the Regulatory Affairs department.

Your primary accountabilities:

You'll be supporting the Regulatory Affairs concepts and strategy for the worldwide registration of all Alcon devices of the surgical instrumentation group.

This includes:

  • Preparation and coordination of the documents needed for the worldwide registration and license renewals for medical devices of the surgical instrumentation group.
  • Ensuring that submissions are complete, well organized, scientifically accurate, of high quality and in compliance with regulations
  • Update and administrative maintenance of technical documentation / global dossiers
  • Management of RA Product Master Data and worldwide registration data in the relevant systems for new registrations, renewals and data maintenance during product life cycle
  • Administrative maintenance of all regulatory documents incl. their archiving
  • Organization and execution of all administrative tasks within the Regulatory Affairs department

Your profile:

Bachelor in life sciences, work experience in Quality Assurance or Regulatory Affairs would be an asset

  • Proficiency in MS Office
  • Fluent English and German language skills (verbally & written) are mandatory
  • You are well organized, pragmatic, solution-oriented, and a team player in a multicultural environment

Your application

Are you interested? We look forward to receiving your application.

Please apply online. For more information about this position, please contact your Kelly recruiter Ms. Susanne Junker (+41 76 335 16 58),

You can find other interesting positions on our website: