49 Junior Qa jobs in Egypt

**Project** Description**:
Luxoft DXC Technology Company is an established company focusing on consulting and implementation of complex projects in the financial industry. At the interface between technology and business, we convince with our know-how, well-founded methodology and pleasure in success. As a reliable partner to our renowned customers, we support them in planning, designing and implementing the desired innovations. Together with the customer, we deliver top performance!

For one of our Clients in the Insurance Segment we are searching for a Senior QA.

**Responsibilities**:

- Do you have an eye for detail? Do you have a 'test to break' attitude? We are looking for someone like that who can:
- Be a part of a User Acceptance Testing and QA Engineering Team
- Work with development team and business representative have a substantial impact on quality of deliverables
- Improve and extend existing testing methodologies including automated solutions
- Define test scenarios based on business requirements
- Ensure the highest quality of deliverables
- Create test plans and perform planning activities
- Analyze complicated financial system, confirm its behaviour with client and business experts and implement detailed documentation of the product

**Skills**:
Must have
- Technical Test Automation experience (4+ years)
- Test Automation - experience with multiple Frameworks
- Tertiary level background in Information Technology
- Agile - Scrum Experience
- Test Analysis, Design and Reporting
- An analytical and logical attitude
- Advanced Level Microsoft Toolset Experience
- Industry Standard Test Management Tool Experience
- Industry Standard Backlog Management Tool Experience

Nice to have
- Insurance industry know-how (portfolio management, claims, mortgage)

**Languages**:
English: C1 Advanced

**Seniority**:
Senior

**Relocation package**:
If needed, we can help you with relocation process.

Vacancy Specialization

QA automation

Ref Number

VR-81169

**Project** Description**:
Luxoft DXC Technology Company is an established company focusing on consulting and implementation of complex projects in the financial industry. At the interface between technology and business, we convince with our know-how, well-founded methodology and pleasure in success. As a reliable partner to our renowned customers, we support them in planning, designing and implementing the desired innovations. Together with the customer, we deliver top performance!

For one of our Clients in the Insurance Segment we are searching for a QA Lead.

**Responsibilities**:

- Employ a range of techniques to analyse problems and evaluate multiple solutions against engineering, business & strategic criteria
- Identify and resolve barriers to business deliveries implementing solutions which iteratively deliver value
- Design solutions using common design patterns with a range of design tools & techniques
- Design & build solutions which are secure & controlled
- Strong end to end Agile process delivery.
- Database analysis and sequel query skills.
- Strong Quality Assurance Automated Testing Skills
- Strong background in Regression/Functional/Volume Testing
- Able to automate testing for RESTful APIs; Messaging; and RDBMSs
- Nice to have xperience with testing tools such as Python pyautogui or BluePrism (RPA) experience
- Experience with git and TeamCity or Jenkins.

**Skills**:
Must have
- Strong Java and/or.NET and/or Angular skills.
- Database analysis and good sequel query skills.
- Strong end to end Agile process delivery.
- Strong Quality Assurance Automated Testing Skills
- Strong background in Regression/Functional / Volume Testing
- Experience in the usage of Tools that support Quality Assurance Testing

Nice to have**Languages**:
English: C1 Advanced

**Seniority**:
Lead

**Relocation package**:
If needed, we can help you with relocation process.

Vacancy Specialization

QA automation

Ref Number

VR-81213

**Company**: MCV INDUSTRY ( egypt)
- **Job Purpose**:
Responsible for verifying and reviewing the quality systems applied to ensure their compatibility with required standards guided by the estimated cost and time set

**Job Duties and Responsibilities**:

- Implement quality assurance standards, processes and control quality assurance standards
- Evaluate production capabilities and recommends improvements
- Assist in developing quality assurance policies and procedures
- Maintain proper documentation and reports
- Organize all audits activities, which include internal, suppliers, distributors and external audits
- Participate in building and updating the quality management system (QMS),
- Promote interest in quality improvement efforts by publicizing product results
- Coordinate with line audits and technical department to ensure making the required corrective and preventive action and avoid non
- compliance with the required product specifications and codes
- Maintain quality records in accordance with the requirement of ISO 9001
- Fulfill additional tasks as per job requirements and as directed by line management

**Job Skills and Abilities**:

- Excellent in English language
- Very good communication skills
- Very good computer skills
- Ability to work under pressure
- Multi task Engineer

**Qualifications**:

- BSC in Mechanical Engineering Preferable (Power or Production)
- 3 - 6 Years of Experience

**Duties & Responsibilities**:

- Conducting regular investigations to guarantee that workers’ follow safety procedures as required
- Conducting quality audits as required to ensure compliance with GMP, Quality standards.
- Performing pre and post-production quality checks and providing related reports accordingly.
- Carrying out the issuance and weighing process of raw materials to guarantee the conformity of specifications to quality standards, approving the release of materials to production, as well as ensuring compliance of raw material storage with regulatory guidelines
- Ensuring compliance of plant conditions (Humidity, Temperature, etc) with set guidelines
- Checking machine conformity to standards as well as ensuring periodic maintenance implementation
- Performing other duties related to the job as assigned by the direct supervisor

**Job Requirements**
- Bachelor’s degree of Pharmacy.
- At least 1:2 years of experience in similar position.
- Ability to work with a team and being an effective team member
- Good understanding in the QA processes and the Agile development process
- Knowledge of quality assurance terminology, methods, and tools

**Job title:** QA Validation Officer
**Location:** Cairo Site
**Hiring Manager:** Quality Assurance Validation Section Head
**About the job**
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
**Job Purpose:**
To ensure that all validation activities comply with regulatory requirements, industry standards, and company policies to guarantee product quality and patient safety.
**Tasks and Responsibilities:**
**Issuing & following up of Validation Master Plan (VMP):**
Issuing the VMP.
Archiving of finished document with necessary attachments.
**Following up & updating implementation by various departments** ·
Performing of Manufacturing, Packaging Processes Validation:
Reviewing of updates in current SANOFI guidelines to check for changes.
Creating of validation protocols to include validation objective, scope, responsibilities, critical parameters, acceptance criteria, sampling locations to be conducted during validation.
Monitoring & checking the various activities during production processes & ensuring that they are as mentioned in both Processing batch record & validation protocol.
Sampling according to validation protocol & providing QC with samples.
Collecting data from the various departments, analyzing information provided & preparing report to include results & conclusion of validation.
**Performing of Cleaning Validation** :
Studying the design of the machines &determine the critical points for cleaning.
Initiating the protocols & follow up distribution to concerned department after approval of concerned managers.
Following up of sampling process.
Preparing of the report showing the results of cleaning validation
**Reviewing of GMP documents** :
Reviewing Master BMRs SOPs, etc. & Ensuring the HSE approval if required.
Updating our GMP documents according to the last updated |GQDs directives & guidelines.
**HSE** :
Follow the laboratory safety procedures o Commitment to the appropriate PPE use.
Follow the approved HSE policy and requirements.
Following the statutory legislation concerning Health, Safety and environmental law.
Hydrocarbons/ hazardous substance & waste segregation in accordance with approved waste management system
**Others:**
Perform other duties as assigned. o Respect of company's values, code of ethics and social charter. Respect of personal data protection charter.
Responsible for applying the HSE related requirements for the company in all related working procedures.
**Requirements/Qualifications**
2-5 years of related experience
preferred bachelor's degree in Pharmaceutical Science
**Soft skills** ·
Good communication & Presentation skills.
Planning & organizing skills. · Problem solving skills.
Report writing skills.
Ability to co-ordinate several inter-departmental activities.
Good command of MS Word, Excel & Power Point.
Technical skills ·
Good Manufacturing Practices (GMP) & Good Documentation Practices (GDP).
Languages · English · Arabic
**Play To win Behaviors:**
+ Stretch to go beyond the level we have operated at up until now.
+ Take actions instead of waiting to be told what to do.
+ Act in the interest of our patients and customers
+ Put the interests of the organization ahead of my own or those of our team
**Pursue** _Progress_ . **Discover** _Extraordinary_ .
Progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let's pursue progress. And let's discover extraordinary together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (

**Siemens Digital Industries Software - Where today meets tomorrow.**

Let's make the difference together!
**Meet the team - **Video**

Siemens DISW is a global technology powerhouse. With some of the best-known brands in the world, Siemens has stood for engineering excellence, innovation, quality, and reliability for more than 165 years.

**Design-to-Silicon D2S**, is seeking a highly qualified **Software Test Engineer **for a position within **Calibre RET QA Team in **Cairo, Egypt.

**Responsibilities**:

- Sponsors quality process and procedures throughout the entire product lifecycle including inspections, code reviews, requirements, code coverage and quality improvement.
- Set expectations for product quality, create a plan to measure the expectations, and ensure execution of the plan.
- Accountable for the predictability of schedules and measuring progress to goals against objectives.
- Understands the level of quality required at different phases of the product lifecycle and ensures that the product works in the customer intended environment. Works with customers, marketing, and/or Customer Support to understand customer needs and requirements.
- Record past verification and validation efforts to ensure reproducibility of results.
- Assesses technical capability of product, including ease of use, functionality, reliability, and serviceability.
- Testing product for defects and limitations, and boundaries (think of all the ways that a product might not work).
- Collaborates and coordinates as needed with global engineering and QA teams.
- Review functional and design specifications and other project documentation. Review internal and external product and release documentation and provide appropriate input to others, e.g. KPD, third party providers, etc.
- Coordinate efforts with SW Development and Release Team members to ensure quality software releases.

**Qualifications**:

- B.Sc./M.Sc. in in Electrical Engineering Electronics and Communication/Computer Engineering.
- ** 3 to 5 years of experience** in testing and test automation.
- Good knowledge in Linux/Unix OS., Versioning control tools (CVS, git), Bash, Python, TCL and Defect Tracking Systems.
- Good to have DRC, Standard verification rule format (SVRF) and Calibre tools.
- Good knowledge of IC manufacturing process and IC layout design.
- Good Knowledge of Software Quality Assurance processes and software testing concepts is an asset.
- Excellent communication skills and ability to work closely with product owner and R&D to understand software features and customer usage.
- Self-Motivated engineer with good capability for continuous learning.

We offer a comprehensive reward package which includes a competitive basic salary, bonus scheme, and generous holiday allowance.

Siemens is an equal opportunities employer and do not discriminate unlawfully on any grounds. We are committed to providing access, equal opportunity.

Siemens. Making real what matters
**If you want to make a difference - make it with us!**

**Organization**: Digital Industries

**Company**: Mentor Graphics Egypt Company (A Limited Liability Company - Private Free Zone)

**Experience Level**: Experienced Professional

**Full / Part time**: Full-time

**MultiCare** Egypt for Pharmaceutical Industries is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, gender identity or expression, age disability, or other characteristics protected by prevailing regulations, practice or customs/traditions.

**MultiCare** is a well-established Pharmaceutical Company with diversified scope in both manufacturing and marketing of pharmaceutical products, supplements, cosmetics and medical devices. Multicare has +21 years of prominent existence in the local market and has almost +69 products marketed and more to come through the pipelines. **MultiCare** Egypt for Pharmaceutical Industries is the manufacturing facility which located at the Industrial Zone - New Cairo and its HQ close by the facility at New Cairo as well. We are one of the fast growing Pharmaceutical Companies in the market which has strong ambition and aspiration to be one of the key players not only in Egypt but also within the region.

Our international alliances are effective in different countries, including Saudi Arabia, United Arab of Emirates, India and New Zealand with future aspiration to extend more business associations and affiliations in near future to further markets. Recently Multicare Poland has been launched which will be the entry port of the business to the European Union (EU).

**QA Manager Vacancy**:
Multicare Egypt for Pharmaceutical Industries is seeking for a Quality Assurance Manager as per the following details:

- **Designation **: QA Manager
- **Location **:3rd Settlement, New Cairo, Kattamia (Industrial Area), Cairo
- **Reporting**: Site Manager
- **Grade**: qAm01/qAm02

**Job Purpose**:
To lead the Quality Assurance function through its staff ensuring full and strict adherence and compliance to the the cGMP, Policies, Procedures, and Prevailing local and international guidelines instilling the quality in the heart of everything QA Team do.

**A. Essential Duties and Responsibilities**:

- Lead the efforts of QA personnel responsible for the testing, investigations, and method transfer activities to ensure compliance with all regulatory requirements, company policies, values, and goals
- Responsible for setting strategy direction for the Quality Assurance Dept. and team
- Provide leadership for lot release, incoming quality, manufacturing, and labs investigations, change control and corrective and preventative action review/approval, manufacturing support, record review/approval, and ongoing projects support (if any)
- Support team by guidance and coaching and provide direction/approval of activities and decisions
- Cultivate and reinforce appropriate group values, ethics, norms, and behaviors
- Share oversight to individuals and team on personal development, performance, and quality related issues. Write and deliver performance reviews
- Ensure proper use of assets, budget, and personnel and communicate effectively with key customers and partners, both within the site and outside as appropriate
- Responsible for supporting all planned and unplanned manufacturing and labs deviations, review and approval of product and equipment change controls (including SOPs and master batch records)
- Conduct impact assess to design changes and participate/coordinate CAPA Review Board
- Maintain the structure to ensure that all quality commitments and timelines are tracked and met. In addition, assist the senior leaders at the site in resource and budget preparations
- Responsible for driving process improvements within Drug Substance, Drug Product, Site support systems
- Actively with urgency when necessary to resolve issues related to production or supply as it relates to investigations or other issues
- Coordinate planned and/or ad-hoc external audits and drive Internal Audit plan and share reports and outcome to the Site Management Team proposing continuous improvement action plan
- Responsible for driving cross-training across Drug Substance, Drug Product, Site staff resources (as well as potentially other areas of QA)
- Work directly with internal and external customers to assure Best-in-Class expectations for quality are met if not exceeded
- Analyze trends, quality metrics and other data to identify quality and compliance gaps
- Participates in the recruitment, selection, promotion, and performance management of QA employees

**B. Qualification/Knowledge/Experience**:
**Level of Education**:

- Pharmacy graduate preferably with related post-graduate QMS degree or otherwise relevant

**Experience**:

- Track record of leading the QA function at sound pharmaceutical organizations

**Language**:

- Excellent verbal, written and interpersonal communication skills. English fluency essential

**IT Literacy**:

- MS-Office

**C. Competencies and Behaviors**:

- Previous experience mentoring and coaching experienced Quality professionals
- Proven results using quality improvement tools and techniques to drive imp

We are looking for a full-time QA Engineer to work on a project for 5 months with these requirements:

- A bachelor's degree in computer science or related field.
- Up-to-date knowledge of software test design and testing methodologies.

Working knowledge of manual test techniques and compatibility with various software programs. Basic Automatic experience.
- Working knowledge of programming.
- Excellent communication and critical thinking skills.
- Good organizational skills and detail-oriented mindset.
- Good time-management skills.
- Great interpersonal and communication skills.

**Job Type**: Contract

**Salary**: Up to E£700.00 per month

Application Question(s):

- When you'll be available for a call tomorrow?

Review and analyze system specifications.
- Collaborate with software engineers to develop effective strategies and test plans.
- Execute test cases and analyze results.
- Identify test methods and prepare test plans for new or updated software projects to make sure
- Contribute in writing user manuals and other required documents.
- Evaluate product code according to specifications.
- Create logs to document testing phases and defects.
- Report bugs and errors to development teams.
- Help troubleshoot issues.
- Conduct post-release/ post-implementation testing.
- Work with cross-functional teams to ensure quality throughout the software development lifecycle.
- Attend management meetings.
- Track program performance after implementation to prevent the occurrence of errors and problems and ensure efficiency.
- Suggest design improvements or modifications during the development process.

**Qualifications**:

- BSc. of Computer Engineering graduate or equivalent.
- 1+ years of experience.
- Excellent knowledge of design patterns and object-oriented concepts.
- Good knowledge of software QA methodologies, tools and processes.
- Good problem solving skills.
- Ability to learn new technology.
- Ability to write clean code.
- Familiarity with Mac OS or Linux is a plus.

**Benefits**:

- Competitive salary.
- Flexible hours.
- Free food and drinks.
- Friendly Environment.
- Access for a lot of online courses.
- Sessions and talks on IT technologies and Business to increase the knowledge of our employees.
- Fun Environment (PlayStation 4, playing puzzles together).

**Working Conditions**:

- Location: Alexandria, Egypt.
- Days Off: Friday and Saturday.