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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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- Dewan SoftGiza·
- Conduct visual inspections and functional tests on raw materials, in-process products, and finished goods according to established quality standards.
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- Fidia Farmaceuticiمصر·
- Founded in 1946, Fidia is an Italian multinational pharmaceutical company, with R&D, manufacturing, marketing and sales capabilities, and an extensive product…
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- Hikma Pharmaceuticals PLCGiza·
- Method development for the new products.
- Performs analysis of method validation for new products & re-registration.
- Data recording & revision for AR results.
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- SanofiCairo·
- Knowledge of relevant Regulations, Guidelines, both national, regional, and international applicable to affiliate operations, Good Manufacturing Practice (GMP),…
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- Hikma Pharmaceuticals PLCGiza·
- Supply Chain (Production Planning, Logistics & Purchasing).
- Sixth of October City, Badr City & Beni Swief City (transportation and meals are covered).
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- Abbott LaboratoriesCairoTypically responds within 1 day·
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- German International UniversityCairo·
- Good Manufacturing Practices (GMP) in the pharmaceutical industry.
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- AumetAlexandria·
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- Julpharمصر·
- Strong understanding of pharmaceutical market dynamics, regulatory requirements, and industry trends.
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- Vitabiotics EgyptAlexandria·
- BSC degree in pharmaceutical science or Bachelor of science- Understanding of the pharmaceutical industry.
- Effectively Operate the production process under GMP…
- Orchidia Pharmaceutical IndustriesCairo·
- Analyze service quality and customer satisfaction.
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- Vitabiotics EgyptAlexandria·
- BSc. Of Engineering- experience, preferably in pharmaceutical industries.
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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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