astra domain was triggered too early. This is usually an indicator for some code in the plugin or theme running too early. Translations should be loaded at the init action or later. من فضلك اطلع على تنقيح الأخطاء في ووردبريس لمزيد من المعلومات. (هذه الرسالة تمّت إضافتها في النسخة 6.7.0.) in /home/vacappqp/public_html/wp-includes/functions.php on line 6114Validation Engineer At GSK Egypt Location: Giza, Egypt Job description Site Name: Egypt – Giza – Giza Posted Date: Feb 18 2024 Are you looking for an opportunity to manage equipment validation for a manufacturing production line in accordance with GSK policies? If so, this is the role for you. As a Validation Engineer you […]
Validation Engineer At GSK Egypt قراءة المزيد »
Senior Quality Control Analyst At GSK Egypt Senior QC Raw and Packaging Analyst Job description Site Name: Egypt – Giza Are you a Senior QC Raw and Packaging Analyst who is energized by the challenge of being part of one of the leading pharmaceutical companies worldwide? If so, this Senior QC Raw and Packaging Analyst
Senior Quality Control Analyst At GSK Egypt قراءة المزيد »
Chemist At Grupo AJE Location:6th of October, Al Jizah, Egypt Company Description Grupo AJE is the 5th largest Latin multinational and one of the world’s largest drinks brands. We are looking for skilled individuals who are passionate about joining our revolutionary brand and beverage team. If you’re looking for a fulfilling career with great opportunities,
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QA specialist At Indomie Egypt Indomie Egypt is a leading company in FMCG industry now hiring ( QA specialist ) #Job_requirement : • Bachelor Degree. • Experience from 1 to 3 years at same position at FMCG industry • Very Good in English. • Excellent command of Microsoft Office Word & Excel. • Excellent Communication
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Quality Control Analyst At Viatris Egypt Job Description: Every day, we rise to the challenge to make a difference and here’s how the “Quality Control Analyst” role will make an impact: Key responsibilities for this role include: Conduct routine and non-routine analyses of in-process materials, finished goods, or stability samples in a timely manner. Interpret
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QA Vacancy At Utopia pharmaceuticals Job Title: IPQA Specialist Company: Utopia Pharmaceuticals Location: 10th of Ramadan City, Egypt Job Description: We are seeking a dedicated and detail-oriented IPQA Specialist to join our team at Utopia Pharmaceuticals. The ideal candidate will have 1 to 3 years of experience in the pharmaceutical industry, specifically in IPQA (In-Process
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Open Vacancies At Future Pharmaceutical industries 1-QC Raw material analyst Duties: Preparation of working standard Preparation of test solutions and volumetric solutions Analysis of RM, PP and SP performed with lab instruments and wet chemical assays according to pharmacopeia Writing report of analysis for release Assist in creation of test method and work sheet Operating
Open Vacancies At Future Pharmaceutical industries قراءة المزيد »
Quality Assurance Engineer At Harvest Foods We are looking for a Quality Assurance Engineer to join our team Location: Industrial Zone, 6 October, Job Description: • Strong personal motivation and drive to learn and continually improve self and company. • Conducts continuous follow-up during the shipment of products to agents and export customers from the
Quality Assurance Engineer At Harvest Foods قراءة المزيد »
Microbiologist At Marbella For Food Industry Job Description Perform sampling and microbiological examination of raw materials and packaging materials. Perform microbiological examination of finished products. Isolate and identify microorganisms by microscopic examination, morphological characteristics, and biochemical reactions. Perform data entry and maintain all department records and documents according to current procedure and write certificate for
Microbiologist At Marbella For Food Industry قراءة المزيد »
Quality Assurance Supervisor At Orchidia Pharmaceutical Calibration and Qualification Supervisor At Orchidia Pharmaceutical Job Description Issue and maintain validation master plan and calibration plan. Write validation protocols and reports. Perform validation activities described in validation protocols including thermal studies, equipment and utilities validation. Responsible for clean room qualification activities for classified areas and LAF
Quality Assurance Supervisor At Orchidia Pharmaceutical قراءة المزيد »
