Kinetic is working with a leading Medical Device company who are hiring a Regulatory Affairs Specialist to be based in Egypt.
Please note that you must meet all the criteria set out below for your application to be considered. Suitable candidates will be contacted within 5 working days. If you are not contacted by us within that time, please consider your application unsuccessful on this occasion.
The main responsibilities will include but not limited to:
- Ensures timely preparation, submission, and appropriate follow-up of new applications to the local authorities.
- Maintenance of assigned, authorized products through timely submission of variations, and renewal applications.
- Track and follow up with the submission of regulatory files (renewals, variations, etc.)
- Ensures high-quality labeling translation and artwork management.
- Updated on relevant local regulations and guidelines.
- Maintain a positive relationship with internal and external regulatory contacts.
To be successful you will need to meet the following:
- Only Candidates currently based in Egypt will be considered.
- Bachelor’s Degree in Pharmacy or related field.
- Minimum 3-5 years regulatory experience.
- Regulatory affairs experience within the Medical Devices Industry is a must.
- Good knowledge of regulatory requirements, regulations & guidelines for medical devices.
- Scientific knowledge and strong attention skills.
- Must have excellent verbal and written communication skills in English and Arabic.
Must Read: How to Create an ATS-Friendly CV That Will Accelerate Your Career.
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