Job Description
Jamjoom Pharma has in a very short span of time emerged, as one of the leading pharmaceutical companies in the Afrasia region. The geographical focus of the company is on countries in the Middle East, Africa, and CIS regions. Strategic focus on selected therapeutic categories has contributed to the rapid growth, market acceptance, and overall success of the company.
Role Purpose:
Responsible for managing all deviation reports including investigation and CAPA management, performing risk assessment required for any process, handling of customer complaints, within the ALJP factory and assure compliance with the WHO cGMP, FDA& EDA regulations.
Responsible:
- Responsible for deviation handling system including, investigations and CAPA Management process to ensure its effective closure in timely manner in addition to its effectiveness.
- Lead & participate in risk management process in all facility areas & set appropriate mitigation actions.
- Handle customer complaint system including, investigations and CAPA Management process to ensure its effective closure in timely manner in addition to its effectiveness.
- Handle CAPA system management to ensure its effective closure in timely manner in addition to its effectiveness.
Qualifications :
- University graduate pharmacy, or science.
- 4-6 years of relevant experience in sterile manufacturing in the pharmaceutical industry.
- No less than 3 years in a similar position.
- Up-to-date knowledge of Good Manufacturing Practices and related local regulations.
- Working knowledge in FDA, WHO and ICH guidelines.
- Excellent investigation and report writing skills.
