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