OBS! Ansökningsperioden för denna annonsen har
passerat.
Arbetsbeskrivning
For products within defined responsibility, including but not limited to:
- Manage the core and local regulatory dossiers, life cycle management and compilation of
submissions for medicinal products.
- Creation and/or review of regulatory documentation relevant for submission
- Maintain current knowledge base of existing and emerging regulations, standards, or guidance
documents.
- Provide regulatory input to cross functional teams/projects.
- Co-ordinating subsidiaries, partners and consultants on applicable market(s)
- Regulatory project lead when relevant.
- Product Information - creation, revision and translations to local languages.
- Ensure updates of applicable national databases and product monograph websites
- SOP development and maintenance.