Project Manager Regulatory Submissions

Vor 6 Tagen


Deutschland JobGet Vollzeit
About the Role

We are seeking a highly skilled Regulatory Affairs Manager to join our team at JobGet. As a key member of our organization, you will be responsible for preparing and submitting maintenance- and life-cycle activities for medicinal products, including variations, renewals, and PSUR submissions.

Key Responsibilities
  • Coordinate projects, including project-related decision-making and reporting
  • Coordinate project teams with internal stakeholders and external suppliers
  • Prepare, review, revise, and maintain regulatory documents
  • Monitor internal and external deadlines
  • Manage data in regulatory databases
Requirements
  • University degree or professional training with RA experience
  • Good knowledge of the legal framework for regulatory affairs for medicinal products in the EEA
  • Very good command of German and English
  • Ability to work independently
  • Very good communication and interpersonal skills
What We Offer
  • Open corporate culture with fast decision-making processes
  • Individual development and training opportunities
  • Flexible working hours and mobile working
  • Job ticket for the RMV region and Job Bike
  • Childcare allowance
  • Health-promoting offers
  • Additional benefits


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