Regulatory Affairs Specialist
Due to recent expansions, Rameda Pharmaceuticals is hiring
Job title: Regulatory Affairs Specialist
Job location: Cairo Scientific Office - Mohandesin
Duties and responsibilities:
- Prepares registration files for products
- Liaises with Ministry of Health to get the registration files accepted and follows up with the different committees of the Ministry to get their approvals until having the final approval for market release with the products validation time
- Planning and Monitoring of the Regulatory Context
- Registration of new products & re-registration of current products
- Maintain and update labeling & variations, carry out the planned RA Activities e.g. Pack Size Additions, Artwork Approvals, Preparation & submission of BE files with follow up with the third-party center and Health Authority
- Assure compliance with internal audit files
- Price Preparation, submission & follow up of files and documents in the required Timelines.
- Following and complying with all the defined internal policies and procedures of working.
- Strictly follows all the Authority Regulations, decisions & decrees.
Job Requirement:
- Bachelor's degree in Pharmaceutical Sciences.
- 1-3 experience in pharmaceutical companies
- Active, organized, planner and able to work within teams
- Good communication skills
- High Level of commitment and reliability
- Fluency in English
- Strong communication skills in both English and Arabic
- Good computer skills
Interested candidates, kindly send your CV to:
Abeer.fathy@rameda.com
with the job title in subject line
#job #pharmaceutical #pharmacists #regulatory_affairs
Job title: Regulatory Affairs Specialist
Job location: Cairo Scientific Office - Mohandesin
Duties and responsibilities:
- Prepares registration files for products
- Liaises with Ministry of Health to get the registration files accepted and follows up with the different committees of the Ministry to get their approvals until having the final approval for market release with the products validation time
- Planning and Monitoring of the Regulatory Context
- Registration of new products & re-registration of current products
- Maintain and update labeling & variations, carry out the planned RA Activities e.g. Pack Size Additions, Artwork Approvals, Preparation & submission of BE files with follow up with the third-party center and Health Authority
- Assure compliance with internal audit files
- Price Preparation, submission & follow up of files and documents in the required Timelines.
- Following and complying with all the defined internal policies and procedures of working.
- Strictly follows all the Authority Regulations, decisions & decrees.
Job Requirement:
- Bachelor's degree in Pharmaceutical Sciences.
- 1-3 experience in pharmaceutical companies
- Active, organized, planner and able to work within teams
- Good communication skills
- High Level of commitment and reliability
- Fluency in English
- Strong communication skills in both English and Arabic
- Good computer skills
Interested candidates, kindly send your CV to:
Abeer.fathy@rameda.com
with the job title in subject line
#job #pharmaceutical #pharmacists #regulatory_affairs
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