Open Vacancies At BioMED Egypt
1- Documentation specialist
• BioMED Egypt for Pharmaceutical Industries has been operating in the Egyptian market since 2013 with a team of more than 1000 employee and Two ISO certified manufacturing facilities producing different variety of high-quality products covering wide range of therapeutic segments & very rich pipeline targeting to support the Egyptian patients with high quality and affordable products.• Due to BioMED expansion and the plan of launching new products in different therapeutic segments, we are pleased to announce the following job opportunities for
• Responsibilities:
Document Control: Establish and maintain document control processes and systems to ensure all documents are properly created, reviewed, approved, and archived.
• Document Management: Organize, catalog, and file documents, records, and data in both physical and electronic formats, ensuring easy retrieval and accessibility.
• Version Control: Monitor and manage document versions, ensuring that the most current versions are readily available and obsolete documents are appropriately archived.
• Compliance: Ensure all documents comply with relevant industry regulations, standards, and internal quality guidelines.
Qualifications:
• Bachelor degree in sciences or pharmaceutical sciences.
• 1-2years of experience in decument management, informtion management.
• Excellent organizational skills and attention to detail
• Proficient in using office software and decument managementtools(e.g.Microsoft office, SharePoint, decument control software).
• Effective communication skills, both written and verbal.
If you want to be part of our professional team and actively contribute to BioMED expansion and success, please send us your updated C.V in PDF to the following E-mail
Recruitment@biomed-egy.com
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2-Validation Specialist:
• BioMED Egypt for Pharmaceutical Industries has been operating in the Egyptian market since 2013 with a team of more than 1000 employee and Two ISO certified manufacturing facilities producing different variety of high-quality products covering wide range of therapeutic segments & very rich pipeline targeting to support the Egyptian patients with high quality and affordable products. • Due to BioMED expansion and the plan of launching new products in different therapeutic segments, we are pleased to announce the following job opportunities for
Responsibilities:
• Validation Protocol Development: Create, review, and execute validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). • Data Collection and Analysis: Collect and analyze validation data to ensure compliance with established standards and specifications.
• Documentation: Maintain accurate and comprehensive validation documentation, including validation plans, reports, and traceability matrices.
• Change Control: Collaborate with cross-functional teams to assess and validate changes to systems, equipment, or processes.
• Responsible for execution of cleaning validation
Take part in any validation related activities as holding time validation protocols.....etc
Qualifications:
• Bachelor degree in sciences or pharmaceutical sciences.
• 1-2 years of experience in validation, preferably.
•Excellent analytical and problem-solving skills.
• Attention to detail and a commitment to quality.
• Add knowledge of statistical package is a plus.
• Mention in the subject the job title any other cv without subject will be discarded automatically.
If you want to be part of our professional team and actively contribute to BioMED expansion and success, please send us your updated C.V in PDF to the following E-mail
Recruitment@biomed-egy.com
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3- In process control
BioMED Egypt for Pharmaceutical Industries has been operating in the Egyptian market since 2013 with a team of more than 1000 employee and Two ISO certified manufacturing facilities producing different variety of high-quality products covering wide range of therapeutic segments & very rich pipeline targeting to support the Egyptian patients with high quality and affordable products.• Due to BioMED expansion and the plan of launching new products in different therapeutic segments, we are pleased to announce the following job opportunities for Responsibilities:
• Real-time Monitoring: Continuously monitor production processes, equipment, and parameters to identify deviations or issues that may impact product quality.
• Data Analysis: Collect and analyze data from in-process inspections and tests to ensure products meet established quality specifications.
• Process Optimization: Collaborate with production teams to implement process improvements and corrective actions to address quality issues.
• Documentation: Maintain accurate and comprehensive records of in-process inspections, deviations, and corrective actions.
Qualifications:
Bachelor degree in science or pharmaceutical sciences.
0-1 years of experience in in-process control, quality assurance, or related roles within
amanufacturing or production environment.
·
Knowledge of quality systems is a plus
Preferably male.
• Send your Updated C. V in PDF
• Mention in the subject the job title any other cv without subject will be discarded automatically.
If you want to be part of our professional team and actively contribute to BioMED expansion and success, please send us your updated C.V in PDF to the following E-mail
Recruitment@biomed-egy.com