Regulatory Affairs Coordinator 100% (f/m)


Standort:

Zürich

Gepostet am:

Juni 12, 2018

Beschäftigungsart:

Temporärarbeit

Referenznummer:

06680-0010488345

Bereich:

Assistenz/Kaufmännisch


Description

For one of the world's leading medical company in Zurich we are currently looking for a Regulatory Affairs Coordinator 100% (f/m).

Your Responsibilities

  • Establish and maintain a close corporation with international partners
  • Processing regulatory assessments of changes by sending out to international partners, monitoring and summarizing responses
  • Drafting and proof-reading of summary technical files documents
  • Create templates in word and excel for regulatory letters, statements, submission requirements, SOPs
  • Maintenance of master data
  • Support in maintenance of documentation in SAP
  • Searches for information and evaluation of information, uploading of documents
  • Data extraction, filing and archiving of submissions
  • Preparation of documents and reports
  • Proofread submission documents and final check before regulatory release of products
  • Administrative SAP support for article listing and delisting

Your Qualification and Skills

  • Bachelor of Administration is an advantage
  • Technical or scientific background
  • At least 5 years work experience in regulatory affairs within the medical industry
  • Experience of data entry and maintenance in a business (SCM) environment
  • Experience SAP
  • Strong analytical skills
  • MS Office experience (proficient Excel user)
  • Strong English communication skills, both written and verbal
  • Effective interpersonal and communication skills
  • Ability to meet timelines and work accurate

Are you interested in this position?

Please apply online giving the reference number 06680-0010488345 in your application. If you need any further information on this role, please contact Alexandra Kowollik from Rbert Half Office Team.



Zürich

Bahnhofplatz 9 Zurich, 8001 +41 (0)43 344 76 00
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