Jamjoom Pharma Egypt Vacancies
Senior Finished Product Specialist at Jamjoom Pharma
Jamjoom Pharma Egypt is looking to hire (Senior Specialist - Finished Product) to join the Quality Department in its new factory in Obour city.
Interested candidates who match the below criteria are kindly requested to send an updated CV to the below email, mentioning the Job Code (S-FP) in the subject field. Only emails with job codes will be considered. Best of Luck.
Brief Duties and Responsibilities:
1- Creation of SOPs related to finished products systems.
2- Creation of SPECs and Methods of Finished products.
3- Analysis of Finished products.
4- Ensuring Retained samples are delivered to laboratory with analysis samples.
5- Recording practical tasks according to GMP requirements and existing systems.
6- Management of HPLC columns.
7- Aware with equipment qualification.
8- Can Perform method transfer protocols.
Job Requirement:
- Egyptian.
- Bachelor’s degree of Pharmacy or Science.
- 1- 3 years of relevant experience in pharmaceutical industry.
- Up-to-date knowledge of current GMP, GLP, EDA requirements, WHO and ICH guidelines.
- Familiar with Statistical tools (Minitab) and excellent user for Microsoft.
- Working knowledge in Microsoft Office applications.
- Excellent communication skills including fluency in English written and spoken.
- Hard worker, team player, and adaptable to business change.
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Senior Raw Material Analyst at Jamjoom Pharma
Jamjoom Pharma Egypt is looking to hire (Senior Analyst – Raw Material) to join the Quality Department in its new factory in Obour city.
Interested candidates who match the below criteria are kindly requested to send an updated CV to the below email, mentioning the Job Code (SA-RM) in the subject field. Only emails with job codes will be considered. Best of Luck.
Brief Duties and Responsibilities:
1- Creation of SOPs related to raw material system and packaging material system.
2- Creation of SPECs and methods of raw and packaging materials.
3- Analysis of raw and packaging materials.
4- Ensure that correct sampling plans are executed by lab sampler.
5- Ensure that retained samples are withdrawn with analysis samples.
6- Record practical tasks according to GMP requirements and existing systems.
7- Management of Reference and working standards.
8- Responsible for Calibration of TOC.
Job Requirement:
- Egyptian.
- Bachelor’s degree of Pharmacy or Science.
- 2 - 3 years’ experience in QC labs of a pharmaceutical manufacturing facility is a MUST.
- Up to date knowledge of current GMP, GLP, EDA requirements, WHO and ICH guidelines.
- Working knowledge in Microsoft Office applications.
- Excellent communication skills including fluency in English written and spoken.
- Hard worker, team player, and adaptable to business change.
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Compliance First Line Manager at Jamjoom Pharma
Jamjoom Pharma Egypt is looking to hire (Compliance First Line Manager) to join the Quality Department in its new factory in Obour city.
Interested candidates who match the below criteria are kindly requested to send an updated CV to the below email, mentioning the Job Code (CMP-FLM) in the subject field. Only emails with job codes will be considered. Best of Luck.
Brief Duties and Responsibilities:
1-Lead the Compliance activities in the Quality Assurance Department to ensure achievement of agreed-on objectives.
2-Lead CAPA Management process to ensure effective and timely completion.
3-Ensure planned change controls are effectively handled in a correct manner as per SOPs
4-Manage company Internal audits and ensure effectiveness of self-inspection Processes.
5-Manage Site inspection lead hosting audits.
6-Handle and manage site compliance issues.
7-Ensure that all deviations/incidents are investigated, assessed, and appropriately corrected.
8-Ensure local and global regulatory conformance and alignment.
9-Ensure deployment of global references and their effective implementation.
Job Requirements:
· Egyptian.
· Bachelor’s degree of Pharmacy.
· 4 - 6 years of relevant experience in Sterile manufacturing in pharmaceutical industry.
· Up-to-date knowledge of Good Manufacturing Practices and related local regulations.
· Working knowledge in WHO and ICH guidelines.
· Preferably familiar with SAP system.
· Excellent documentation and report writing skills.
· Great attention to details and promotes quality work standards.
· Committed and able to work within team.
· Good Leadership skills and ability to influence others.
· Excellent communication skills including fluency in English written and spoken.