jamjoom pharma jobs
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- Jamjoom PharmaCairoTypically responds within 1 dayEmployerActive 15 days ago·
- Responsible for providing evidence that all information necessary to determine that the product fit for the intended use is gathered evaluated & approved.
- Jamjoom PharmaCairoTypically responds within 1 dayEmployerActive 7 days ago·
- To ensure consistent sales growth and achievement of goals and targets of our Pharmaceutical business in the assigned regions, while collaborating with other…
- View all Jamjoom Pharma jobs - القاهرة jobs - Medical Representative jobs in Cairo
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- Jamjoom PharmaCairoTypically responds within 1 dayEmployerActive 6 days ago·
- Monitoring the safety profiles of our marketed products and addressing any.
- Prepare and Submit PV New Drug/Device Application.
- Bachelor’s degree in pharmacy.
Job Post Details
Quality Assurance- IPC Executive (Egypt)
Job details
Job type
- Full-time
Location
Cairo
Full 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.
About the job:
- Responsible for providing evidence that all information necessary to determine that the product fit for the intended use is gathered evaluated & approved. To involve, coordinate & control the activity that fulfill the quality requirements.
Responsibilities:
- Ensure proper sampling of intermediate, bulk, and finished product batches for routine testing, and cleaning samples.
- Follow up the application of quality assurance measures in production areas and check compliance with IPC testing.
- Ensure implementation of procedures of batch manufacturing and packaging documents, specifications & SOPs.
- Ensure application of quality assurance measures during validation batches and planned changes.
- Monitor calibration of production equipment and IPC testing instruments.
- Review batch related documentation for completeness, correctness, and compliance to approved standards.
- Report any observed incidents during routine production and follow-up its correction and corrective action.
- Ensure that GMP Standards are followed properly in the Warehouse, Dispensing and manufacturing areas and during the manufacturing and packaging processes.
- Participate in deviations, complaints, OOSs & OOTs in coordination with area owners and ensure implementation of CAPA and closure within the required timeline.
- Performing APR activities
- Ensure that the requirements for data integrity at the site are in place by conducting spot audits.
Qualifications:
- 2-5 years’ experience in pharmaceutical Quality assurance in sterile & non sterile manufacturing.
- Master’s degree / bachelor’s degree in pharmacy.
- Excellent interpersonal, communication skills , team playing capability & ability to meet challenges & deadlines.
- Excellent documentation and report writing skills.
- Up-to-date knowledge of Good Manufacturing Practices , SFDA and related local regulations.
- Fluency in Arabic & English languages.
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