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 Job Vacancies at Jamjoom Pharma Egypt

Job Vacancies  at Jamjoom Pharma Egypt



Jamjoom Pharma is looking to hire (IPC Specialist) in the Quality department in its new factory in Obour city-Egypt.

Interested candidates who match the criteria are kindly requested to send an updated CV to the below email mentioning the Job Code (IPC-SP) in the subject field. Only emails with job codes will be considered.

egypt.jobs@jamjoompharma.com

· IPC testing during all steps of product manufacturing in accordance with governance SOPs

· Ensure proper sampling of intermediate, bulk and finished product batches for routine testing, validation practices and cleaning samples.

· Follow up application of quality assurance measures in production areas and check compliance of 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 deviations, complaints, OOSs & OOTs in coordination with area owners and ensure implementation of CAPA and closure within required timeline.

· Ensure identification and rejection of non-conforming materials/products according to GMP standards.

· Coaching operators to ensure that quality mindset is embedded in their day to day activities.


Required Qualification/Experience:

* Egyptian.

* Bachelor's degree of pharmacy or science.

* 1- 3 years experience in similar field especially in sterile pharmaceutical areas.

* Up-to-date knowledge of current GMP, EDA Regulatory requirements, WHO & ICH guidelines.

* knowledge with SAP system is preferred.

* Familiar with IQ, OQ, PQ, facility, utilities, Equipment and Strong experiences in cGMP/GLP compliance activities. 

* Excellent documentation and report writing skills.

* Excellent communication skills including fluency in English written and spoken.

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Jamjoom Pharma is looking to hire (Calibration Engineer) in the Validation department in its new factory in Obour city-Egypt.

Interested candidates who match the criteria are kindly requested to send an updated CV to the below email mentioning the Job Code (CAL-ENG) in the subject field. Only emails with job codes will be considered.

 

egypt.jobs@jamjoompharma.com

  

Duties and responsibilities: 

-Act as system owner/subject matter expert for the calibration process. 

-Conduct calibration activities in adherence to the schedule and procedures. 

-Maintain oversight of the outsourced calibration providers.

-Collaborate closely with various departments to contribute to efficient performance. 

-Own Calibration SOPs and Methods. Undertake review and sign-off when required. 

-Undertake development Calibration activities and advise on troubleshooting. 

-Ensure Calibration activities are documented clearly and followed in accordance with Jamjoom pharma documented procedures and GMP requirements and Good Engineering Practices. 

-Adhere to site and corporate quality system requirements for calibration systems within utilities, facilities manufacturing and laboratory areas. 

 

Required Qualification/Experience

* Egyptian.

* Bachelor’s degree in Engineering/Science.

*2-4 years of relevant experience in a validation engineering role in pharmaceutical industry.

*Experience and knowledge in a testing, calibration, or qualification environment and conversant with calibration regulations. 

*Knowledge of Pharmaceutical calibration and GMP requirements. 

*Ability to influence and collaborate at all levels to achieve quality targets. 

*Project coordination experience is a plus. 

*Strong troubleshooting skills.

*Excellent communication skills including fluency in English written and spoken.


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Jamjoom Pharma is hiring the below positions in Validation team in its new factory in Obour City-Egypt.

Interested candidates who match the below criteria are kindly requested to send an updated CV to the below email; mentioning the Job Code in the subject field. Only emails with job codes will be considered.

 

egypt.jobs@jamjoompharma.com


1-Cleaning Validation Senior Specialist (Job Code: CL-SP)

-Schedule, plan, and execute studies for cleaning validation activities for large and small equipment, media fill and gowning qualification.

-Generate, execute, and review master and completed cleaning validation protocols, media fill protocols, gowning qualification protocol, summary reports, associated data, deviations for conformance to regulations, SOPs, specifications, and other applicable acceptance criteria.

-Investigate and troubleshoot problems that occur and determine solutions or recommendations for changes and/or improvements

-Review, edit, and approve deviation notifications, deviation investigations, and corrective actions.

-Review, edit, and approve change controls, SOPs, reports, and other documentations.


2- Process Validation Senior Specialist (Job Code: PCS-SP)

-Experience in a cGMP regulated manufacturing environment, with exhibited knowledge or proficiency in process validation. 

-Author validation documentation including, but not limited to SOPs, Process Validation/Verification/Assessment Protocol & Report. 

-Write validation protocols/reports and other documentation related to the activities Based on the deduced CQAs (Critical Quality Attributes) and CPPs (Critical Process Parameters) be able to develop the needed process validation strategy, sampling strategy.


3-Qualification Senior Specialist (Job Code: QL-SP)

-Provide expertise in validation ensuring compliance with current industry regulations, guidelines, and trends. 

-Reviews master and completed qualification and validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications, etc. 

-Run qualification of premises, equipment, and utilities [URS, DQ, IQ, OQ and PQ]. 

-Run Computer system validation, Laboratory equipment qualification. 

-Ensure change controls are assessed for impact on validation. 

-Review and approve validation master plans.

-Execute validation protocols when required, including preparation and review of deviations associated with validation activities.



Required Qualification/Experience


* Egyptian.

* Bachelor’s degree of Pharmacy or Science.

*2 - 4 years of relevant experience in Validation field in pharmaceutical industry.

*Understanding of manufacturing processes and related process equipment.

*Great attention to detail and promotes quality work standards.

*Ability to compute, analyze, and interpret statistical data.

*Committed and able to work within team.

*Problem Solving Skills.

*Excellent communication skills including fluency in English written and spoken.

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