Regulatory Affairs Coordinator - Medical Device
Location
Remote
- Job ID
- ZW5257
- Date posted
- 03/20/2026
- Category
- Regulatory Affairs
- Job Facet 1
- Lorem Ipsum
- Job Facet 2
- Lorem Ipsum
- Job Facet 3
- Lorem Ipsum
Regulatory Affairs Coordinator (Contract, EMEA Region)
We are seeking a detail-oriented and proactive Regulatory Affairs Coordinator to join our team and provide essential administrative project support for our ongoing regulatory transition activities. This is an excellent opportunity for someone with prior experience in managing high-volume documentation within the life sciences or medical device sector, especially those with knowledge of AGILE systems.
Key Responsibilities:
- Collect, organize, and maintain regulatory documentation (e.g., technical files, IFUs, labels, product portfolios)
- Support MDR/IM updates in collaboration with local EMEA Regulatory Affairs colleagues
- Work within document management systems such as Windchill, MDRIM, and AGILE
- Raise and track internal requests, ensuring timely follow-up and resolution
Preferred Experience:
- Prior hands-on experience with the AGILE system
- Ability to quickly adapt to complex regulatory environments and manage multiple priorities
Position Details:
- Start Date: ASAP
- Contract Duration: 12 months from start date
- Location/Time Zone: EMEA region preferred; applicants from Turkey, South Africa, and Egypt are welcome
If you are ready to support high-impact regulatory projects and have the documented experience we seek, we invite you to apply now and join a dynamic, global team!
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