351 Quality Assurance Specialist jobs in Egypt

Company Description

MICO WORLD is an Internet company specializing in the social entertainment industry. It has developed several popular social entertainment applications, including MICO, YoHo, TopTop, and SUGO. With a strong presence in markets like the Middle East, Southeast Asia, North America, Japan, and Korea, MICO WORLD operates in over 150 countries and regions. The company boasts over 200 million global registered users of its products.

Role Description

This is a full-time on-site role for a Quality Assurance Specialist - Live streaming, located in Cairo, Egypt. The Quality Assurance Specialist will be responsible for conducting quality control and assurance tasks, ensuring compliance with quality standards, and implementing quality management practices. Day-to-day tasks will include monitoring live streaming content, performing quality audits, and ensuring adherence to Good Manufacturing Practice (GMP).

Qualifications

• Quality Control, Quality Assurance, and Quality Management skills
• Quality Auditing skills
• Excellent attention to detail and problem-solving skills
• Strong communication and teamwork abilities
• Relevant experience in the live streaming or social entertainment industry is a plus
• Fluency in English

Mumzworld
, founded in 2011, is a leading e-commerce platform in the Middle East region, specializing in mother, baby, and child products. The company prides itself on its comprehensive catalogue of products delivered in the fastest, most convenient, and cost-effective manner. With a focus on creating a positive social impact, Mumzworld empowers mothers through informed purchase decisions and a supportive bilingual community.

Key Requirements:

• Bachelor's degree in Business Administration, Communications, or related field (preferred).
• 3 years of experience in customer service, with 1-2 years of experience in the same role
• Solid understanding of customer service best practices, especially in e-commerce.
• Strong analytical and problem-solving skills.
• Ability to deliver clear, constructive feedback and maintain confidentiality.
• Excellent verbal and written communication skills in both internal and external settings.
• Proficient in Microsoft Office and quality monitoring tools.

Core Competencies:

• Customer Obsession
• High Standards & Attention to Detail
• Coaching & Feedback
• Analytical Thinking
• Process Improvement
• Adaptability & Ownership
• Stakeholder Management
• Problem Solving
• Developing Others
• Continuous Improvement Mindset

Work Location and Compensation

• Net Salary is 17 to 19K EGP + 80$ KPI's after passing probation

• 100% onsite - shifts and day-offs are rotational

• Location: Abbassya, Cairo

About Minapharm:

Minapharm Pharmaceuticals is a leading pharmaceutical company in Egypt and the Middle East and the largest end-to-end manufacturer of biological therapies in MEA with over 20 years of experience in cellular and bioprocess engineering. Headquartered in Cairo, Minapharm commercializes over 100 lifesaving and life-enhancing products ranging from small molecules to complex bioengineered proteins and viral vectors, with an impressive immunotherapy pipeline. Together with its wholly owned Berlin-based subsidiary, ProBioGen AG - a world-leading CDMO, Minapharm has established an integrated business model making it the only gene-to-market company in the region. Consolidating its international platform of intelligent biopharmaceutical technologies with the longstanding process development and manufacturing expertise in the MEA, Minapharm, together with ProBioGen, has incorporated MiGenTra GmbH headquartered in Berlin and manufacturing in Cairo, to enhance the accessibility to critical healthcare transforming medicines through product development and commercialization of Biosimilar mABs, Cell, and Gene Therapies and vaccines, at affordable prices in Egypt, and MEA.

Our Values:

• Diversity & Respect
• Integrity & Accountability
• Collaboration
• Leadership & Empowerment
• Innovation & Continuous Learning

QA Compliance Specialist Job Summary:

Perform all quality assurance compliance activities including but not limited to GMP and pharmaceutical quality system compliance, gap analysis, internal audits, supplier audits, PQR, complaints, quality risk management and GMP training.

QA Validation Specialist Job Summary:

To execute qualification and validation for all manufacturing and cleaning procedures.

QA Compliance Specialist Duties & Responsibilities:

1. Participate in update procedures relevant to pharmaceutical quality system compliance, gap analysis, internal audits, supplier audits, quality risk management and GMP training.
2. Participate in annual internal audit schedule, prepare internal audit reports, send approved internal audit reports to owners, agree with owners on SMART CAPAs, follow up closure of CAPA and evaluate CAPA effectiveness and quarterly report status of internal audit QKPIs.
3. Participate in audits of supplier / contractor / contract acceptors, prepare audit reports, send approved audit reports to supplier / contractor / contract acceptors, agree with them on SMART CAPAs, follow up closure of CAPA and evaluate CAPA effectiveness and quarterly report status of supplier / contractor / contract acceptors audit QKPIs.
4. Ensure that all employees (permanent, temporary) and contractor / visitors receive required GMP training before they independently certified to perform their tasks independently.
5. Prepares a register of qualified trainers, participate in preparation of training programs, participate in evaluation of training effectiveness and quarterly report status of GMP training QKPIs.
6. Participate in all quality risk management activities with cross-functional teams of SMEs. Follow-up closure of all actions required to reduce risks to an acceptable level and evaluate effectiveness of these actions through after-action risk review. Quarterly report status of quality risk management QKPIs.
7. Work with cross-functional team to develop and maintain site contamination control strategy. Prepare a quarter report indicating status of contamination control strategy and its effectiveness in controlling contamination and cross-contamination risks and recommendations for improvement.
8. Perform PQR data collection, review, analysis and reporting for all manufactured products. Set recommended actions and required SMART CAPA with follow up closure of CAPA and evaluate CAPA effectiveness and quarterly report status of PQR reports in QKPIs.
9. Handling of received Customer Complaints ( starting from receiving of complaint, numbering, evaluation and investigation, impact assessment, set SMART CAPA, immediate action and CAPA follow up, closure and trending )
10. Participate in different multidisciplinary teams and relevant activities as required.

QA Validation Specialist Job Responsibilities:

1. Follow equipment calibration plan and coordinate with concerned departments to perform qualification/validation activities.

2. Witness equipment qualification/calibration activities and review qualification documents and calibration certificates supplied by external service providers.

3. Prepare protocols, execute qualification protocols and report outcomes for process and cleaning validation in addition to Equipment / Utilities qualification.

4. Issue new SOPs and revise SOPs as requested.

5. Record incidents, deviations, changes and participate in the investigation and assessment.

6. Implementation of CAPA, additional controls, change control actions, annual report actions, management review actions.

7. Execute quality risk management-projects, health and safety risk-assessment and environmental aspects & impacts.

8. Perform on-site training sessions as relevant.

Needed qualifications:

• 1-3 years in pharmaceutical industry preferably experience in quality operations & in sterile manufacturing, hands on experience in validation activities.
• Minimum BSc in pharmaceutical sciences is a must.
• GMDP requirements for sterile biological products.
• Ability to implement and follow-up of validation or qualification requirements.
• Ability to evaluate data generated from validation studies.
• Basic GMP.
• Proficiency in English language.

Job Location:
10th of Ramadan.

• Transportation is provided.
• Medical Insurance.
• Life Insurance.
• Profit share.

Good Luck to All

Main Tasks:

• Conduct audits across all departments, including Customer Service, Sales, Customer Experience, Operations, and Back Office.
• Ensure compliance with company policies, industry regulations, and quality benchmarks.
• Identify process gaps, inefficiencies, and risks, recommending corrective actions and improvements.
• Monitor the implementation of quality assurance measures and maintain accurate documentation of audit findings.
• Provide data analysis and performance reports to senior management, highlighting trends and areas for improvement.
• Develop strategies to enhance operational efficiency, service quality, and compliance.
• Deliver training sessions, refresher courses, and coaching to employees on quality standards, audit procedures, and best practices.
• Mentor and support teams to ensure adherence to operational protocols.
• Customer Service & Quality Monitoring:
• Conduct quality assessments of customer interactions (calls, emails, and chats) to ensure service excellence.
• Implement quality assurance procedures to enhance customer experience and satisfaction.
• Work closely with teams to address quality-related issues and customer concerns.
• Collaborate with department heads to optimize processes and streamline operations.
• Stay updated on industry trends, regulatory changes, and best practices to drive continuous improvement.

Requirements:

• Bachelor's degree in a relevant field.
• From 1 to 3 years of experience in quality assurance, auditing, or process improvement.
• Strong analytical, problem-solving, and reporting skills.
• Excellent communication and interpersonal abilities.
• Familiarity with quality standards, compliance regulations, and operational audits.
• Holds a Quality Certification or has completed a relevant course (e.g., Lean Six Sigma, TQM, or ISO 9001 Auditor Certification) is preferred.

Interested candidates please send your CV to with Quality Assurance Specialist in the subject.

Job Type: Full-time

Application Question(s):

• What is your current and expected salary?

Experience:

• Quality Assurance: 1 year (Preferred)

Company Description

Farmex has been growing, processing, and exporting premium quality fresh fruits and vegetables from our soil lands in Egypt since 2007. Managed by a highly qualified team and supported by a strong logistics department, Farmex ensures top-notch product handling. The company stays up-to-date with trends in product preparation, packing, and quality, ensuring excellence beyond expertise and experience.

Role Description

This is a full-time on-site role for a Quality Assurance Specialist located in Alexandria, Egypt. The Quality Assurance Specialist will be responsible for overseeing quality control processes, ensuring compliance with quality standards, conducting audits, and managing quality assurance activities. The role also involves monitoring good manufacturing practices (GMP) and maintaining high standards in product quality.

Qualifications

• Global Gap , HASSSAP , ISO Certificates Experience
• Quality Control and Quality Assurance skills
• Experience in Quality Management
• Knowledge of Good Manufacturing Practice (GMP)
• Quality Auditing skills
• Strong analytical and problem-solving abilities
• Excellent attention to detail and organizational skills
• Ability to work effectively in a team-oriented environment
• Bachelor's degree in Quality Management, Food Science, or a related field is preferred

Job Summary:

We are seeking a detail-oriented and proactive Quality Assurance Specialist to

join our QA team. You will play a crucial role in maintaining compliance with

industry regulations and internal quality standards, ensuring the safety and

consistency of our products throughout the production lifecycle.

Duties and Responsibilities:

• Monitor and assess the performance of the quality systems, report their effectiveness to management, and implement actions for improvement.

• Ensure compliance with the audit programs for internal and external audits for ISO 9001:2015, ISO 14001:2015, ISO 45001:2018 and ISO 17025

Ensure plant compliance with Good Manufacturing Practices (GMPs).

• Drive non-conformity management and verify the effectiveness of action plans through follow-up on customer complaints across all product categories and ensure that CAPA implementation is communicated back to the markets.

• Maintaining the calibration and verification processes in compliance with the standard requirements considering plan, instrument lists, certificates, verification forms, and service providers communications. -0olllp'.

• Promote quality awareness and ownership across the value chain.

• Follow up on the objectives of departments.

Required Reports:

• Internal Audit Protocol.

• Weekly ABC report.

• NCR.

• Customer Complaint Register.

Work Communications:

Internal (Departments and purpose of communication)

• Departments, head, and EBC employees

• Quality Assurance Supervisor.

• Quality Manager.

External (Third Party and purpose of communication)

• 3rd Party for inspection.

Qualifications:

• Bachelor's degree in chemistry, Chemical Engineering, or related field.

• 2 to 3 years of QA experience in a chemical manufacturing or regulated industry.

• Strong knowledge of QA/QC protocols, GMP, ISO 9001, or similar quality systems.

• Excellent attention to detail, organizational, and communication skills.

• Thorough knowledge of methodologies of quality assurance and standards.

• Strong knowledge of MS Office and databases, and Minitab.

• Outstanding communication skills.

• Excellent organizational and leadership abilities

• Certification of ISO standard is a strong advantage (ISO 9001, 45001, etc.).

• Ability to work cross-functionally in a fast-paced environment.

Job Type:

• Full time (On-Site)

• Working hours from 8 am to 5 pm.

• Two days off (Friday and Saturday).

-
Yearly Profit Share, Private Medical Insurance, Merits, Monthly Incentives, Transportation, Housing.

Company Description

COB Solution is dedicated to empowering medical providers with efficient operations, optimized workflows, and innovative solutions. Our approach is designed to enhance patient care and accelerate growth. We focus on providing quality and effective solutions to meet the unique needs of healthcare providers.

Role Description

This is a full-time on-site role located in Qesm El Maadi for a Quality Assurance Specialist. The Quality Assurance Specialist will be responsible for overseeing the quality control processes, and conducting quality audits. Additional duties include implementing and managing quality management systems, developing quality assurance protocols, and collaborating with cross-functional teams to ensure regulatory compliance and product quality.

Qualifications

• Quality Control and Quality Assurance skills
• Experience in Quality Management and developing quality protocols
• Experience in conducting Quality Audits
• Strong analytical and problem-solving skills
• Excellent written and verbal communication skills
• Bachelor's degree in a related field such as Quality Management, Biotechnology, or similar
• Experience in the healthcare or medical device industry is a plus
• Attention to detail and ability to work independently

Requirements

Practical experience in Quality Management Systems (ISO BRC or equivalent).

Ability to develop and implement QA procedures and inspection reports.

Strong follow-up and internal auditing skills.

Proficiency in Microsoft Office applications.

Excellent communication and analytical skills.

Company: MCV INDUSTRY ( egypt)-

Job Purpose:

Responsible for leading the quality assurance effort for our products Will be working closely with the development team to ensure that the products meet the highest quality standards

Job Duties and Responsibilities:

• Provide technical expertise on quality
  assurance and quality control-
  Coordinate and execute projects,
  including setting up process flows, identifying and documenting potential
  issues, generating testing strategies, developing and maintaining test scripts,
  and providing valuable QA feedback to developers
• Analyze product and process
  specifications and procedures
• Identify and recommend major
  improvements to procedural and business processes
• Develop quality assurance standards and
  processes
• Perform other duties as assigned
• Recommend changes or improvements to
  existing processes, methods, and technologies that improve product quality,
  safety, productivity, and customer satisfaction
• Develop and conduct test plans and test
  cases, including test scripts, results, execution, shared responsibilities,
  deadlines and test environment
• Implement test plans and test cases, and
  supervise inspections and testing of components, sub-assemblies, or for
  packaged software
• Develop test cases based on requirements
  and implement test plans to assure software meets project specifications and
  design
• Perform exploratory testing with a focus
  on identifying and documenting defects
• Review defects and test logs to identify
  root causes and suggest solutions for improving testing, documentation, and
  process improvement
• Perform research and write new test
  cases
• Document test data and results
• Understand product lifecycle concepts
  and participate in the test planning process

Main KPI Key Performance indicators:

• Core Competencies
• Financial Management
• Customer Excellence
• Process Management
• Growth & Development
• Functional Competencies
• Job Knowledge
• Monitoring, Reporting and Trend Thinking
• Technology and Cyber Security
• Leadership Competencies
• Accountability & Focusing on Business Results
• Emotional Intelligence
• Integrity & Professional Behavior

Job Skills and Abilities:

• Previous experience in quality assurance or similar field
• Working knowledge of tools, methods, and concepts of quality assurance
• Solid knowledge of relevant regulatory standards
• Good communication skills, both verbal and written
• Effective written and verbal English communication skills
• ISO experience

Certificate in quality assurance is a plus

Qualifications:

• Bachelor's degree from any discipline
• More than two years proven experience as an QA specialist in a fast-paced environment
• Expert knowledge of technical design processes, flowcharting techniques, and code compliance
• Strong attention to detail