🚀 We’re Hiring! Join El Teriak’s Growing Team

El Teriak is expanding, and we’re looking for talented professionals to join our dynamic organization. If you’re passionate, driven, and ready for the next step in your career, we want to hear from you!

📍 Location: 6 October

- Manufacturing manager

- Planning Manager

- Production Manager

- Quality manager

📩 Apply Now:

careers@elteriak.com

Join EVA Pharma is hiring:

Vaccine Quality Assurance Specialist

Job Summary

We are seeking a passionate and talented Vaccine Quality Assurance Specialist to join our dynamic team.

The ideal candidate will ensure that all vaccine manufacturing and handling processes meet the highest standards of quality and compliance, supporting our mission to enhance human health and well-being.

Key Responsibilities:

- Monitor environmental conditions (temperature, humidity, pressure differentials) across vaccine production and storage areas, ensuring compliance with GMP requirements.

- Participate in raw material dispensing for vaccine manufacturing and verify specifications and calculations as per SOPs.

- Oversee vaccine manufacturing and packaging operations to ensure adherence to GMP, SOPs, and data integrity requirements.

- Review batch records and logbooks related to vaccine production for completeness, accuracy, and compliance with GDP.

- Record and report deviations, non-conformities, and incidents specific to vaccine processes. Participate in root cause investigations and track corrective and preventive actions (CAPA).

Requirements:

- Bachelor’s degree in Pharmacy.

- 0–2 years of relevant experience in pharmaceutical QA; experience in vaccine manufacturing is a plus.

- Knowledge of cGMP and GDP principles.

- Understanding of CAPA, change control, and quality documentation systems.

- Familiarity with ISO 9001 and safety programs.

- Awareness of validation principles and basic statistical concepts.

Apply now!

https://lnkd.in/d3sFAvjj

GET Group Holdings Ltd. is hiring:

Senior QA Specialist 

📍 Location:

Sheraton Cairo

🕒 Employment Type: Full time/Hybrid

Key Responsibilities:

1. Ensure that each project is following the standard processes and using all related templates (taking into consideration the tailoring sheet if it exists) by conducting Process and Product QA audits as per the QA schedule for each project.

2. Prepare the QA Audit Non-compliance Report (NCR) and suggest corrective actions.

3. Ensure that the QA Audit Non-compliance Report (NCR) corrective actions are implemented by the defined due dates and escalate the status to the QA Manager in case of any delay.

4. Review the project QPM (Quantitative Project Management) workbook

5. Collect and store the validated measurement data as per the frequency defined in project schedule in the Measurement and Analysis sheet.

6. Review the Projects’ Configuration Management plan(s) using the CMP review checklist, record comments in the V&V Tracker and track the defects till closure.

7. Conduct Configuration Management audits on the SW releases and ensure the solving of all NCs before release.

8. Assist in applying any updates in the QMS releases to improve the process.

9. Update the Process Asset Library (PAL) periodically with the projects’ data.

10. Provides QMS Trainings 

Requirements:

* Bachelor’s degree in Engineering or Computer Science

· At least three (3) years of experience in Quality Assurance

· Knowledge of Audit Techniques

· Knowledge of CMMI Quality Standard

· Excellent computer skills, especially MS Office and MS Project

* Excellent analytical and problem-solving skills.

* Strong communication skills in English (Arabic is a plus).

📧 How to Apply:

Send your updated CV to: 

candidate_egy@getgroup.com

👉 Please mention the job title “Senior Software Tester” in the subject line

Join EVA Pharma, 

We are seeking a detail-oriented and organized:

QA Administration & 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:

- Review and approve Quality Assurance documents, including SOPs, specifications, and validation protocols, ensuring compliance with regulatory standards.

- Maintain an organized document control system to manage the lifecycle of quality documents from creation to archiving.

- Support ongoing training initiatives by ensuring that relevant documentation is accessible and up to date.

- Coordinate internal audits for documentation practices and assist in preparation for external audits.

- Collaborate with cross-functional teams to address any documentation-related issues and promote a culture of quality.

Requirements:

-Bachelor’s degree is a must.

- 0-2 years of experience in quality assurance, document control, or regulatory compliance within the pharmaceutical industry.

- Problem Solving and Analytical Thinking.

- Excellent attention to detail and organizational skills, with the ability to manage multiple priorities and meet deadlines.

- Effective communication and interpersonal skills to work collaboratively with various teams.

- Proficient in Microsoft Office Suite and familiar with quality management software.

Apply now!

https://lnkd.in/dJZ4uV9q

📢 We’re Hiring:

𝗤𝘂𝗮𝗹𝗶𝘁𝘆 𝗘𝗻𝗴𝗶𝗻𝗲𝗲𝗿

📍 𝗟𝗼𝗰𝗮𝘁𝗶𝗼𝗻: ElWasta, Egypt (transportation provided)

 🏢 𝗖𝗼𝗺𝗽𝗮𝗻𝘆: Samsung Electronics Egypt

We are expanding our Quality team and looking for highly skilled Quality Engineers who are passionate about driving excellence, reducing defects, and ensuring world-class product quality.

🔎 𝐊𝐞𝐲 𝐑𝐞𝐬𝐩𝐨𝐧𝐬𝐢𝐛𝐢𝐥𝐢𝐭𝐢𝐞𝐬:

•  Conduct inspections, audits, and quality checks on production lines.

•  Analyze defects, scrap, and customer complaints to identify root causes.

•  Implement corrective and preventive actions (CAPA).

•  Ensure compliance with internal and external quality standards.

•  Support cross-functional teams to improve product performance and process stability.

•  Prepare quality reports and dashboards for management.

•  Drive continuous improvement initiatives.

🎓 𝐑𝐞𝐪𝐮𝐢𝐫𝐞𝐦𝐞𝐧𝐭𝐬:

•  Bachelor’s degree in Engineering (Mechanical, Industrial, Mechatronics, or related).

•  Proven experience in Quality Engineering within a manufacturing environment is a plus.

•  Strong knowledge of quality tools (ISO standards, SPC, FMEA, 8D, RCA).

•  Excellent analytical and problem-solving skills.

•  Strong communication skills and teamwork mindset.

💼 𝐄𝐱𝐩𝐞𝐫𝐢𝐞𝐧𝐜𝐞:

 ✔ Minimum 3~5 years of experience in Quality Engineering or Quality Assurance in manufacturing.

Apply here:

🔗 Apply here [https://lnkd.in/dt7eHqC7]

Send your CV to:

alaa.emad@samsung.com

abdallah.sa@samsung.com

Haier Electric Egypt is for home appliances industry -multinational Org is hiring" Quality improvement engineer

Location :10th of Ramadan

Job Title:

Quality improvement engineer 

Industry : home appliances

Job description: 

1. Be responsible for analyzing and resolving market quality issues, and formulate and implement improvement measures;

2. Coordinate internal and external resources to promote closed-loop management of quality issues;

3. Collect and analyze quality data, identify potential risks and propose preventive measures;

4. Participate in the formulation and optimization of product quality standards to ensure compliance with market demands;

5. Maintain good communication with customers, promptly feedback and solve the problems raised by customers.

Job requirements:

-Bachelor’s degree in engineering (Mechanical, Industrial, Electrical, or a related field) or a relevant scientific discipline.

-Proven experience (3-5 years) in a Quality Engineering, Supplier Quality, or Customer Quality role, preferably within a manufacturing or product development environment.

if interested kindly send your cv to: hee.basma.ahmed@haier.com

And mention the title in the subject.

Join EVA Pharma

Job Summary:

We are seeking a passionate and talented

“Quality Control Section Head”

to join our dynamic team in Sudair City - Saudi Arabia. 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.

Key Responsibilities:

- Lead the setting up of QC laboratories and Plan, coordinate, and execute qualification and calibration of QC instruments, as well as Develop laboratory readiness plan to support site commissioning and validation

- Ensure timely and accurate execution of stability studies and method validations, as well as Review and approve analytical data and reports.

- Ensure adherence to cGMP, SFDA, ICH, FDA, EMA, and other applicable regulatory guidelines.

- Maintain and approve SOPs, STPs, specifications, and other QC documentation and Lead investigations for OOS, deviations, and complaints, ensuring CAPA implementation.

- Prepare for and participate in internal and external audits and ensure timely closure of audit observations and CAPAs.

Requirements:

- Bachelor’s degree in pharmacy, Chemistry, or Life Sciences.

- 8–10 years in pharmaceutical manufacturing.

- Saudi Experience is a Must.

- Experience in handling injectables, oral solids, and regulatory audits.

- Strong knowledge of analytical techniques (HPLC, GC, UV, IR).

- Proficient in GMP documentation and data integrity principles.

Apply now! 

https://lnkd.in/dYXrPHMt