Quality

Quality Assurance Vacancy At Al Andalous Pharmaceutical

Quality Assurance Vacancy At Al Andalous Pharmaceutical Title: QA Compliance Senior Specialist (Job Scope) Assure that Al Andalous Quality Management System complies with internal requirements (e.g. quality policy, company manual, sops, specifications, and other quality documents) and external national and international requirements (e.g. guidelines, standards, regulations, and laws). Responsibilities Collection of data of products under […]

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Quality Control Vacancy At Hipharm

Quality Control Vacancy At Hipharm We are hiring QC Specialist Requirements: . BSc. degree in Pharmaceutical science . Minimum one year experience . Perform routine analysis for Raw materials (Active and In Active raw materials) received from the warehouse according to the controlled work instructions . Perform routine chemical analysis for water samples . Follow

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Chemist At Medizen Pharmaceutical Industries

Chemist At Medizen Pharmaceutical Industries Medizen Pharmaceutical Industries is seeking to hire the following position: ” Microbiology specialist “ *Job Requirements: -Bachelor degree in science ( Microbiology Department ) -Excellent computer skills and data analysis knowledge. -Very good English language -” Males only “ – Only candidates from Alexandria – Experience needed: Fresh graduated *Working

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Quality Graduate Program At Froneri Egypt

Quality Graduate Program At Froneri Egypt Quality Control Management Trainee – Graduate Program Our Graduate Program is a learn by doing experience in a fast-paced environment, designed to provide fresh graduates with the exposure and knowledge they need to get prepared for the market. FRONERI is hiring Quality Control Management Trainee in the Production department.

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Quality Vacancy At Hikma Pharmaceuticals

Quality Vacancy At Hikma Pharmaceuticals Title:  Senior Quality Assurance Officer Description: Job Summary: To assist in fulfilling varying tasks related to quality including assisting supervisors in training analysts, producing batch records, checking laboratory equipment and ordering needed supplies to aid in the production of safe products that meet the company’s specifications.   Job Description: Assists in supervising

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Hikma Internship Program 

Hikma Internship Program Title:  Internship Program 2026 Description: Here’s your opportunity to apply for Hikma Egypt internship program 2026 Applicants can apply to one of the following functions: Quality Validation Quality Control Quality Assurance Accounting & Finance Information Technology Sales Supply Chain (Production Planning, Logistics & Purchasing) Production Production Engineering / Maintenance Internship duration: 1

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QEHS Internship At Kraft Heinz

QEHS Internship At Kraft Heinz Description & Requirements Project Scope The scope of the Integrated Quality and EHS Management System Update Project will encompass the following areas Integration of QMS and EHS Identify common elements and requirements between the QMS and EHS management systems. Develop a cohesive framework that aligns and integrates QMS and EHS

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QA Vacancy At Viatris Egypt

QA Vacancy At Viatris Egypt Quality Assurance Coordinator (Release & Doc.) At Viatris Egypt Position summary: Revision of batch records before product release to ensure compliance with site procedures. Participate in document control process within VIATRIS Cairo site. Participate in preparation, execution and reporting of site validation and calibration activities. Job Specific technical/Functional/Professional Competencies: Batch

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Quality Assurance Vacancy At Hi Pharm

Quality Assurance Vacancy At Hi Pharm Hi Pharm is Hiring! Position: Compliance and Documentation Specialist Requirements: – BSc. degree in Pharmacy or Science – Minimum 1 year of experience in the pharmaceutical field – Knowledge of EDA regulations and standards related to manufacturing processes – Follow up on the implementation of CAPA according to the

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QA Vacancy At Pharaonia Pharmaceuticals

QA Vacancy At Pharaonia Pharmaceuticals Position Title: QA unit Head Key Accountabilities: Design standard operating procedures of the quality assurance department in the sterile area and non-sterile area in accordance with the approved guidelines. Review and approve standard operating procedures for the sterile area in accordance with the approved guidelines. Final approval of batch records

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