Quality Vacancies At U-Pharma
1-Quality Assurance – Documentation and Batch Release Supervisor
Quality Assurance – Documentation and Batch Release Supervisor is urgently Required to join U Pharma’s team.
the Role holder will be based in U pharma’s plant located in 10th of Ramadan city
Brief Duties & Responsibilities:
The position holder is responsible for reviewing and approving of batch record and disposition of finished products.
The scope of activities includes, but is not limited to, supervision of document control function, including document receiving, follow up issuing cycle, distributing, archiving, retrieval of obsolete documents, Batch Record Issuance, review, disposition, archiving, retrieval and disposal.
The position holder will work under a defined SOP and guidelines that need to be fulfilled in addition to continuous improvement of the process.
Requirements:
Quality professional with 5-7 years of hands-on experience in Quality Assurance in Pharmaceutical Sterile industry .
B.Sc. of pharmacy or Science.
Excellent knowledge of GMP and WHO requirements
Experience in document management and trainings.
Very good command of English language.
Very good computer skills (MS office package)
ERP system-based experience – Odoo is an advantage
Very good analytical skills and attention to details.
Residency in 10th of Ramadan city or nearby areas are preferred.
Interested applicants, please send your cv to Recruitment@upharmaegypt.com
mentioning job title (Documentation and Batch Release Supervisor) in the subject line.
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2-Quality assurance - Compliance Supervisor
Quality assurance - Compliance Supervisor is urgently Required to join U Pharma’s team.
the Role holder will be based in U pharma’s plant located in 10th of Ramadan city
Brief Duties & Responsibilities :
Quality Assurance Compliance Supervisor is responsible for participating in the implementation and maintenance of the Pharmaceutical Quality Management System (PQMS) ensuring compliance with pharmaceutical standards and regulations (cGMP & ISO).
The scope of activities includes but not limited to maintaining Pharmaceutical Quality System elements as: CAPA, change management, and non-conformance records, and responsibility of internal & external audits and all PQS elements and enablers.
Requirements:
· Quality professional with 5-7 years of hands-on experience with QMS, GMP and ISO requirements for Pharmaceutical Sterile Manufacturing.
· B.Sc. of pharmacy or Science.
· excellent knowledge of GMP and WHO requirements
· very good command of English language.
· very good computer skills (MS office package)
Residency in 10th of Ramadan city or nearby areas are preferred.
Interested applicants, please send your cvs to Recruitment@upharmaegypt.com
mentioning job title (Compliance Supervisor) in the subject line.