A leading Pharmaceutical company is actively recruiting a Regulatory Affairs & Quality Assurance Specialist – Saudi National for their Riyadh office.
Please note that due to Saudization, only Saudi Nationals can be considered for this role.
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:
- Serve as a link between the company and regulatory authorities ensuring products are manufactured and distributed in compliance with relevant regulatory standards, regulations, and guidelines.
- Support in timely submission and approvals for registration/ re-registration/ variation for various products within the assigned region.
- Facilitates all related technical information and applicable documentation for all submissions.
- Review product and promotional material as requested.
- Support with office license renewal process and scientific office local requirements.
- Provide guidance and support on regulatory and quality requirements to internal teams.
- Lead or support RAQA projects and assignments as required.
To be successful you will need to meet the following:
- Please note that due to Saudization, only Saudi Nationals can be considered for this role.
- Bachelor’s degree in Pharmaceutical Science is a must.
- Minimum 2 – 4 years of experience in Regulatory Affairs and Quality Assurance role in a multinational pharmaceutical company.
- Must have SFDA Experience.
- Experience with International Quality and Regulatory Standards.
- Excellent verbal and written communication skills in English & Arabic.
- Applicants should be available for face-to-face interviews in the location mentioned above.
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