Regulatory Information Administrator

Duties: 

• From varying data sources, identify and extract information regarding the regulatory status of products and/or maintain records
• Coordinate, prepare, and provide information on regulatory status to support local and regional regulatory submissions
• Maintain data integrity of the information on product life cycle management in MS Excel and a Regulatory Information Database
• Assist other members of the team with issues as they arise
• Provide valuable input for the planning and development of a centralized regulatory database system to help identify and align both local and global regulatory organization.
• Assist other members of the team on regulatory work as appropriate

Requirements:

• Successful graduation in a Life Science degree or equivalent
• Medical devices sector experience would be a great plus
• Strong MS Excel skills
• Able to handle and manipulate large excel sheets.
• Very well spoken English

Offer:

• At least a year-length contract for one of the global industry leaders (med-tech)
• Opportunity to access internal know-how and systems
• Data management introduction and onboarding, opportunity to acquire data management skills from great experts
• Attractive salary for those, who have started their professional journey
• Fully remote job