qa administration & document review specialist Jobs in Giza

qa administration & document review specialist

quality assurance officer: (chemist-pharmacist) Jobs in Giza

quality assurance officer: (chemist-pharmacist)

quality audit & verification senior specialist engineer Jobs in Giza

quality audit & verification senior specialist engineer

quality control analyst (contingent worker / temp-to-hire) Jobs in Giza

quality control analyst (contingent worker / temp-to-hire)

supplier quality assurance engineer Jobs in Giza

supplier quality assurance engineer

quality assurance specialist

EVA Pharma

<div>Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members. 
Job Summary 
We are seeking a passionate and talented Quality Assurance Specialist to join our dynamic team.
The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry. 
 
Responsibilities:
<ul><li>Monitor environmental conditions (temperature, humidity, pressure differentials) and ensure they comply with GMP requirements across production and warehouse areas</li>
<li>Participate in raw material dispensing and verify specifications and calculations as per SOPs</li>
</ul><ul><li>Oversee manufacturing and packaging operations to ensure adherence to GMP, SOPs, and data integrity requirements</li>
<li>Review batch records and logbooks for completeness, accuracy, and compliance with GDP (Good Documentation Practice)</li>
<li>Record and report deviations, non-conformities, and incidents. Participate in root cause investigations and track corrective and preventive actions (CAPA)</li>
</ul>
Requirements<ul><li>
Bachelor's degree in Pharmacy.</li><li>
0-2 years of relevant experience in a pharmaceutical QA environment</li><li>
Knowledge of cGMP and GDP principles</li><li>
Understanding of CAPA, change control, and quality documentation systems</li><li>
Familiarity with ISO 9001 and safety programs</li><li>
Awareness of validation principles and basic statistical concepts</li></ul></div>

Quality Assurance Specialist

EVA pharma

<div>
 
 Join EVA Pharma, a leading pharmaceutical company committed to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are dedicated to fostering a supportive and innovative environment for our team members.
 
 
 We are seeking a detail-oriented and organized
 
 QA Administration &amp; Document Review Specialist
 
 to join our dynamic Quality Assurance team.
 
 
 The ideal candidate will ensure that the documentation and records adhere to regulatory standards, while contributing to the overall quality management system.
 
 
 
 
 Key Responsibilities:
 
 
 <ul>
 <li>
 Review and approve Quality Assurance documents, including SOPs, specifications, and validation protocols, ensuring compliance with regulatory standards
 </li>
 <li>
 Maintain an organized document control system to manage the lifecycle of quality documents from creation to archiving
 </li>
 <li>
 Support ongoing training initiatives by ensuring that relevant documentation is accessible and up to date
 </li>
 <li>
 Coordinate internal audits for documentation practices and assist in preparation for external audits
 </li>
 <li>
 Collaborate with cross-functional teams to address any documentation-related issues and promote a culture of quality
 
 
 </li>
 </ul>
 
 Requirements
 
 
 
 
 <ul>
 <li>
 Bachelor's degree is a must
 </li>
 <li>
 0-2 years of experience in quality assurance, document control, or regulatory compliance within the pharmaceutical industry
 </li>
 <li>
 Problem Solving and Analytical Thinking
 </li>
 <li>
 Excellent attention to detail and organizational skills, with the ability to manage multiple priorities and meet deadlines
 </li>
 <li>
 Effective communication and interpersonal skills to work collaboratively with various teams
 </li>
 <li>
 Proficient in Microsoft Office Suite and familiar with quality management software
 </li>
 </ul>
</div>

QA Administration & Document Review Specialist

<div>Join EVA Pharma, a leading pharmaceutical company committed to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are dedicated to fostering a supportive and innovative environment for our team members.
We are seeking a detail-oriented and organized QA Administration &amp; Document Review Specialist to join our dynamic Quality Assurance team.
The ideal candidate will ensure that the documentation and records adhere to regulatory standards, while contributing to the overall quality management system.
Key Responsibilities:<ul>
<li>
Review and approve Quality Assurance documents, including SOPs, specifications, and validation protocols, ensuring compliance with regulatory standards.</li>
<li>Maintain an organized document control system to manage the lifecycle of quality documents from creation to archiving.</li>
<li>Support ongoing training initiatives by ensuring that relevant documentation is accessible and up to date.</li>
<li>Coordinate internal audits for documentation practices and assist in preparation for external audits.</li>
<li>Collaborate with cross-functional teams to address any documentation-related issues and promote a culture of quality.</li>
</ul>
Requirements<ul>
<li>
Bachelor&rsquo;s degree is a must.</li>
<li>0-2 years of experience in quality assurance, document control, or regulatory compliance within the pharmaceutical industry.</li>
<li>Problem Solving and Analytical Thinking.</li>
<li>Excellent attention to detail and organizational skills, with the ability to manage multiple priorities and meet deadlines.</li>
<li>Effective communication and interpersonal skills to work collaboratively with various teams.</li>
<li>Proficient in Microsoft Office Suite and familiar with quality management software.</li></ul></div>

HSE Contractors Inc

Quality Assurance Officer &amp; Quality Control Analyst:(Pharmacy Degree)Multinational company seeks a quality Assurance Officer/ Quality Control Analyst for a 6-month contract in 6th of October City.Responsibilities: Oversee sampling, audits, GMP/ISO/EDA compliance, investigate quality issues, and validate methods.Requirements: Pharmacy degree, 3+ years in QA or pharmaceutical manufacturing, GMP &amp; gas chromatography knowledge, strong English.Living in 6th of October City is preferred.Apply now: Rec.uni2@uni-serve.meJob Type: Temporary Contract length: 6 monthsPay: E&pound;13,000.00 - E&pound;20,000.00 per month

Quality Assurance Officer: (Chemist-Pharmacist)

Nissan

<div>Location: Giza, 6th of October City 
 
Work Arrangement: Onsite 
 
Degree Level: Bachelors 
 
Preferred Degree: Bachelor's degree in engineering/quality or equivalent 
 
Shape the Future of Mobility at Nissan - Launch Your Career, Drive Innovation: 
 
At Nissan, we're not just building cars, we're revolutionizing mobility. We're a global leader with a heritage of innovation, and we're searching for talented individuals like you to join us on this exciting journey. We believe that every individual possesses a unique set of skills and passions that can be harnessed to drive innovation and shape the future of the automotive industry. Our diverse range of program areas and career paths offer exciting opportunities for adventurers like you to embark on a thrilling professional journey.
 
 
Learn more about Nissan's future here: https://www.youtube.com/watch?v=M8diaXXdtJI 
 
We are currently looking for a Quality Audit Verification engineer to join our team at Nissan Motor Egypt. The ideal candidate will play a crucial role in the Total Customer Satisfaction department with quality improvement of NMEG models by conducting audits within the different shops (Trim shop, Body shop, Paint shop and compound). This role is important as it ensures the brand image is enhanced by giving customers quality vehicles. 
 
Main responsibilities: 
<ul><li>
Planning of QAV annual audits within all the relevant departments (imp A&amp;B, Weld, Anti-co, CAMIC, Logistics)</li><li>
Conducting QAV audits in each shop as per the planned schedule (Actual process, documentation)</li><li>
Prevention of future occurrences-Conduct horizontal deployment (confirm and validate NMEG condition based on Japan request</li><li>
Audit follow up (confirm closure of Non-conformances with manufacturing/Quality department)</li><li>
Conduct first line audit compliance check in line with corporate requirements and ensure if there are gaps, they are closed</li><li>
Standard document architecture - ensure adherence of Nissan engineering manuals throughout NMEG plan (All departments)</li><li>
Support and participate in the region/functional requirements (AMIEO Region)- this includes constant communication with the region members (India, UK, NSA)</li><li>
Constant communication/meetings with Japan CZ0 department</li><li>
Monthly reporting to both Japan and Function (AMIEO)</li><li>
Utilize two online systems (drive and AMS) to record non-conformances and close after confirmation</li><li>
Non-conformance validations throughout the shops</li></ul> 

Who we are looking for: 
<ul><li>
Bachelor's degree/Diploma in Engineering/Quality or equivalent</li><li>
Fluency in English and Arabic</li><li>
Automotive manufacturing experience needed</li><li>
Auditing experience is preferable</li><li>
Quality management system knowledge</li><li>
Proficient with MS Office applications (Excel, PowerPoint, Word)</li><li>
Good computer/systems skills mandatory</li></ul> 

Explore more here: https://www.nissanglobal.com/EN/COMPANY/LIFE_AT_NISSAN/ 
 
Fuel your career with innovation and purpose by joining Nissan, a company dedicated to enriching other's lives. 
 
Giza Egypt</div>

Quality Audit & Verification Senior Specialist Engineer

Ariston Group

<div>
 Job description:
 
 
 
 📍 Location: Giza, Egypt
 
 🕒 Full-time
 
 
 
 We&rsquo;re looking for a young professional with a passion for purchasing to join our local team at our manufacturing plant in Giza as Local Indirect Procurement Specialist.
 
 
 &nbsp;
 
 
 
 What You&rsquo;ll Do
 
 
 
 As our Local Indirect Procurement Specialist, you&rsquo;ll be involved in:
 
 <ul>
 <li>
 Supporting internal teams to define needs and assess local market conditions
 </li>
 <li>
 Helping plan purchases to match our technical roadmap
 </li>
 <li>
 Managing the full order process: from technical requirements to negotiation and coordination
 </li>
 <li>
 Ensuring data accuracy and sharing insights across departments
 </li>
 <li>
 Analyzing supplier KPIs and performance (cost, quality, delivery)
 </li>
 <li>
 Participating in cost reduction initiatives and long-term contract negotiations
 </li>
 <li>
 Collaborating with Product Management and Supplier Quality Assurance
 </li>
 <li>
 Engaging local suppliers early in R&amp;D projects
 </li>
 </ul>
 
 &nbsp;
 
 
 
 What We&rsquo;re Looking For
 
 
 <ul>
 <li>
 Recent graduate from a Faculty of Commerce (English section) or graduate from a technical school (preferably Don Bosco Institute)
 </li>
 <li>
 Good English proficiency (written and spoken)
 </li>
 <li>
 Solid Excel and Office skills
 </li>
 <li>
 A data-driven mindset, with strong analytical and organizational skills
 </li>
 <li>
 Negotiation abilities and a proactive attitude
 </li>
 <li>
 Willingness to travel locally
 </li>
 </ul>
</div>

LOCAL INDIRECT PROCUREMENT SPECIALIST

<div>Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.
Job Summary:
We are seeking a knowledgeable and dedicated Microbiology Specialist to join our team.
The ideal candidate will play a crucial role in maintaining the quality and safety of our products through rigorous microbiological analysis and quality assurance.
Key Responsibilities:<ul>
<li>
Conduct microbiological testing on raw materials, in-process samples, and finished products in accordance with relevant regulatory standards</li>
<li>Develop, validate, and implement microbiological testing methods, ensuring compliance with GMP and quality assurance protocols</li>
<li>Monitor environmental conditions within production areas and laboratories, ensuring compliance with microbiological standards</li>
<li>Investigate and resolve microbiological product complaints, deviations, and sterility failures, providing comprehensive reports and recommendations</li>
<li>Support the development and execution of continuous improvement initiatives related to microbiological practices</li>
</ul>
Requirements<ul>
<li>
Master's or Bachelor's degree in Science, Pharmacy, or a related field.</li>
<li>0-2 years of experience in microbiology within the pharmaceutical, biotechnology, or related industries</li>
<li>Strong analytical skills with proficiency in laboratory techniques and equipment.</li>
<li>Detail-oriented with a commitment to accuracy and compliance.</li>
<li>Excellent communication and interpersonal skills.</li></ul></div>

Microbiology Specialist

Explore 161+ Quality assurance specialist in Giza this December. Find roles across top companies and apply now to boost your career.

161 quality assurance specialist jobs IN Giza

Quality Assurance Specialist

QA Administration & Document Review Specialist

QA Administration & Document Review Specialist

Quality Assurance Officer: (Chemist-Pharmacist)

Quality Audit & Verification Senior Specialist Engineer

LOCAL INDIRECT PROCUREMENT SPECIALIST

Microbiology Specialist