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Job Description
- Permanent full time position
- Excellent remuneration package
- Attractive salary
- Annual incentives
- Premium Medical insurance and career development
- Work location:
- Dokki, Giza, Egypt
We are looking for Regulatory Affairs Specialist for our business in Medical Devices and will be responsible for:
- Prepare documents and files to match local registration requirements.
- Present and tracks registration files.
- Negotiate and manage agency agreements with suppliers.
- Meet with authorities' personnel and committees to do all necessary actions in order to push forward the registration/re-registration procedures for the least time possible in order to meet launches dates and customers’ demands.
- Handle all regulations and maneuvers related to pricing in order to get approvals for the Organization desired prices.
- Handle authorities checkups and inspections for conformity with registration regulations.
- Liaise with local and overseas licensors to manage registration regulatory aspects.
- Writing and maintaining procedures for regulatory operations
- Carrying out vigilance reporting and product recalls.
Job Requirements
Successful applicants must have:
- Bachelor of pharmaceutical /sciences/ veterinary medicine.
- At least 2-3 years relevant experience in a health care products registration preferable Medical Devices
- Excellent command of the English language
- Excellent written and verbal communication skills organization and planning
- Problem analysis and problem-solving
- Ability to manage multiple projects and meet the deadlines
- Team-working skills
- Attention to detail
- Persuasiveness, adaptability, judgment, decision-making tolerance & collaboration