Develop Within Regulatory Affairs, Ra Specialist
2 days ago
This role would be a great chance to start your career within Regulatory Affairs department or continue your development and improve your experience and skills to become a successful Regulatory Affairs professional working for a world leader in Medical Devices field.
Regulatory Affairs is a very sought after field and you will be able to learn lots and use this in your career progression in the future.
You will be working with a lot of data, regulatory documents, supporting submissions process, technical review. You will play an important part in local and global regulatory planning and development, data integrity, executing the regulatory strategies.
**Responsibilities**:
From varying data sources, identify and extract required data/documents to create and maintain product records
Provide services to enable execution of regulatory strategies for new projects or changes to existing devices
Maintain data integrity of product lifecycle management
**Requirements**:
Minimum BA degree in Life Sciences or similar
Strong MS Excel skills, managing large excel sheets
Experience with the full cycle of registration - including submissions (Medical Devices)
fluency in English and Arabic
strong database administration experience (Excel, VLOOKUP, Pivot tables)
experience within RA as well as MDR would be great
**Benefits**:
work for a top global employer and boost your experience and CV
hybrid model, working 2 days from home and 3 days in the office in Cairo
competitive package and benefits
This will initially be a 1 year contract with an extension so will suit someone who is open to change for that fairly quickly.
The job market changes very quickly so do not forget to connect with me on Linked in, check other roles that I am hiring for at the moment and follow for any future relevant roles.
Nonstop is dedicated to raising the standard of ethical recruitment and comprises a number of brands, each having their own niche sector focus.
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