Open Vacancies At Global Napi Pharmaceuticals Company
We’re Hiring: Microbiology Senior Specialist & Microbiology Section Head
📩 To apply:
Send your CV to jobs@globalnapi.com
Subject line "Microbiology Senior Specialist" or "Microbiology Section Head"
📍 Location: 6th of October
🚌 Transportation Provided
Microbiology Section Head
• Bachelor's degree in pharmaceutical sciences, Science.
• 7 - 9 years of experience in the same field.
• Have strong leadership, problem- solving, and decision-making skills.
• Strong knowledge of GMP, GLP, and microbiological testing methods.
• Excellent English communication and computer skills.
Microbiology Senior Specialist
• Bachelor's degree in pharmaceutical sciences, Science.
• 3-5 years of experience in the same field.
• Good understanding of GMP, GLP, and regulatory microbiological standards.
• Hands-on experience with microbiological testing and aseptic techniques.
·Strong analytical and problem-solving abilities.
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For the first time at GNP, we are officially launching our Part-Time Medical Representative Program.
This unique opportunity is designed specifically for medical professionals who are eager to leverage their medical expertise into a financially rewarding, part-time career.
It’s a Part Time Job with evening visits only.
📍Cairo East
📍Shoubra
📍Shoubra El Kheima
📍Maadi - Helwan
📍Haram
📍Faisal
📍Imbaba
📍Dokki - Mohandsen
📍Alex East
📍Damnhour
📍Tanta
📍El Menoufia
📍KFS
📍El Minia
📍Assuit
📍Sohag
Send your CV at :
Please mention [Part Time + Area] in the email subject.
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🚨 We’re Hiring: QC Specialist – Finished Product 🚨
📩 To apply:
Send your CV to jobs@globalnapi.com
Subject line "QC Specialist – Finished Product"
📍 Location: 6th of October
🚌 Transportation Provided
We are looking for a QC Specialist – Finished Product to join our dynamic Quality Control team in a pharmaceutical manufacturing facility.
Key Responsibilities:
• Perform quality control testing of finished pharmaceutical products and stability samples according to approved methods and specifications.
• Conduct analysis using HPLC and other analytical techniques.
• Accurately record, analyze, and interpret test data in compliance with GMP and company SOPs.
• Prepare and review analytical reports and certificates of analysis.
• Maintain laboratory instruments and ensure proper calibration and maintenance.
• Participate in investigations of out-of-specification (OOS) and out-of-trend (OOT) results.
• Ensure compliance with GMP, GLP, and safety regulations.
• Collaborate with QA and Production teams to ensure timely product release and continuous improvement.
Qualifications & Experience:
• Bachelor’s degree in Pharmaceutical Sciences or Science (Chemistry or related field).
• 2–4 years of experience in QC of finished pharmaceutical products and stability studies.
• Hands-on experience with HPLC and other analytical instruments.
• Strong English communication skills (written and spoken).
• Proficient in computer applications for data analysis and reporting (e.g., Excel, chromatography software).
If you’re passionate about quality and eager to grow in a pharmaceutical manufacturing environment, we’d love to hear from you!
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We’re Hiring: QA Validation Specialist – Sterile Area
📩 To apply:
Send your CV to jobs@globalnapi.com
with the subject line "QA Validation Specialist"
📍 Location: 6th of October City
🚌 Transportation Provided
We are looking for a QA Validation Specialist to join our dynamic Validation Team in a sterile pharmaceutical manufacturing facility.
Key Responsibilities:
• Support and oversee qualification and validation activities for equipment, utilities, and processes in alignment with GMP standards.
• Lead and participate in risk assessments related to validation and qualification activities.
• Ensure compliance with local and international regulatory requirements (GMP, PIC/S, ISO, etc.).
• Review and approve validation protocols, reports, and related documentation to maintain a validated state.
• Collaborate with cross-functional teams to ensure readiness for audits and inspections, and follow up on CAPAs with different departments.
• Identify and implement continuous improvement opportunities to enhance validation and compliance systems.
Qualifications & Experience:
• Bachelor’s degree in Pharmacy.
• 2–4 years of experience in Quality Assurance / Validation within a sterile manufacturing environment.
• Proven experience in risk assessment and compliance-related QA activities in sterile manufacturing.
• Strong knowledge of GMP principles, validation lifecycle, and regulatory guidelines.
• Excellent English, computer, organizational, and communication skills.
If you’re passionate about quality and eager to grow in a sterile manufacturing environment, we’d love to hear from you!