pharaonia pharmaceuticals jobs
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- PHARAONIA PHARMACEUTICALSAlexandria·
- Daily review of the plant’s plan: Prepare the analysis devices and necessary chemicals to ensure they align with the analysis method for each product.
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- Salary Search: QC Specialist salaries in Alexandria
- PHARAONIA PHARMACEUTICALSAlexandria·
- Coordinating with the weighing and production units to prioritize the manufacturing of high-demand and critical pharmaceutical products.
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- PHARAONIA PHARMACEUTICALSCairo·
- Contribute to the Formulation and development of marketing strategies and programs through a Deep understanding of market trends.
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- PHARAONIA PHARMACEUTICALSAlexandria·
- Preparing tax declarations and adhering to deadlines.
- Performing analysis, reconciliations, and resolving disputes with tax authorities.
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- PHARAONIA PHARMACEUTICALSGiza·
- This role will responsible for generating and enhancing the sales of the products in other countries, And Increase the organization’s profitability by…
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View similar jobs with this employerPHARAONIA PHARMACEUTICALSGiza·- Bachelor’s degree in pharmaceutical sciences, veterinary.
- Achieve the company’s sales objectives for the assigned district (area).
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- PHARAONIA PHARMACEUTICALSCairo·
- Prepare and submit export documentation to regulatory authorities.
- Ensure compliance with international regulations, including FDA, EMA, and other relevant…
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- PHARAONIA PHARMACEUTICALSAlexandria·
- Responsible for electrical maintenance (regular, preventive, corrective, and new installations).
- Apply a production maintenance plan.
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Job Post Details
QC Specialist - job post
Alexandria
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Job details
Job type
- Full-time
Location
Alexandria
Full job description
Job Duties
- Daily review of the plant’s plan: Prepare the analysis devices and necessary chemicals to ensure they align with the analysis method for each product.
- Analysis of products at all stages of manufacturing: Perform chemical analysis using advanced devices (HPLC, G.C., HPTLC) according to the specified analysis methods.
- Re-analyze rejected samples: Recheck the analysis results before rejecting samples and request additional samples for confirmation, informing the direct supervisor.
- Recording in the device logs: Record all details in the devices’ logs used for analysis and submit related reports.
- Report device malfunctions: Notify the direct supervisor about any malfunction of devices during operation.
- Analysis of Holding Time samples: Analyze samples related to holding time studies and issue a report for each study.
- Monitor chemicals and standards: Follow up on the chemicals and standards used for analysis.
- Documenting all department papers: Ensure all department documentation is accurately recorded.
- Follow safety, health, and environmental instructions: Adhere to safety, occupational health, environmental guidelines, and apply GMP, GLP, and S.O.P. regulations.
Qualifications, experience and skills required
- Experience is not required.
- Bachelor’s degree in Pharmacy or Sciences.
- Fluent in English.
- Proficient in computer skills.
- Good communication skills.
- Accuracy, organization, and integrity.
- Ability to work under pressure.
Job Features
Job Category
Quality Control
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