25 Head Qa jobs in Egypt

**About us**:
Convertedin is a marketing operating system for e-Commerce. It utilizes data and shoppers' insights to create personalized multi-channel marketing that boosts customer engagement and maximizes their return on their marketing budget by leveraging artificial intelligence capabilities. Convertedin has helped more than 800 e-Commerce worldwide.

**About the job**:
**Responsibilities**:

- Assess current testing needs and schedules.
- Identify Bugs and Issues with good reporting.
- Execute performance testing.
- Maintain detailed documentation related to the software or system.

**Requirements**:

- Computer Science degree or equivalent.
- Attention to details.
- Strong interpersonal skills, collaboration and self-management.
- Good at object-oriented design concepts, algorithms and data structures.
- Experience in one or more of: C, C++, C#, Objective-C, Swift, Java.
- Familiarity with one or more of: Python, Ruby, Perl, Shell is a plus.
- Familiarity with automated mobile device testing including Apple, Android and Windows.
- Experience in API testing.
- Experience in JMeter or equivalent.
- Familiarity with functional automation tools like Selenium, Appium, Restassured or equivalent.
- Demonstrated problem solving and troubleshooting skills
- Experience in Agile / Scrum project development.

**Benefits**
- Work from Anywhere, yes this remote base opportunity with the availability of hybrid options.
- We love flexibility! Manage your own work schedule. We trust the people we hire.
- Competitive package.
- Paid time off.
- Fun benefits & perks that you will enjoy!
- Trusting, ego-free and truth-seeking team members
- See something you want to improve? Awesome. We’re a flexible and collaborative team that is always learning and growing.
- Need more convincing? Check this out!
- Convertedin is an equal employment opportunity employer such that all qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity/expression, national origin or disability.

**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 is close by the facility as well in New Cairo. 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).

**Vacancy**:
We are recruiting an expert professional to join the QA Team as Quality Compliance Section Head as per the following details:

- **Location **:New Cairo
- **Reporting**:QA Manager
- **Grade**:qAc01/qAc03

**Job Purpose**:
Ensure compliance with cGMP, regulatory, and internal requirements regarding the manufacturing, testing, and distributing of products through formal QA Audits, investigations, training, and recommendations to procedures. Evaluate and provide QA recommendations on all products, systems, and issues that are affected or may be affected by regulatory or cGMP requirements.

**A.Essential Duties and Responsibilities**:

- Ensure a constant state of inspection readiness and that all audit observations are addressed quickly and completely to maintain readiness levels
- Complete minor and major incident investigations in response to any unexplained events encountered during manufacturing or out-of-specification lab results for functional areas. Provide input and guidance to the team conducting the investigation. Make recommendations to department management regarding results of investigation and process improvements, when necessary. Make final recommended batch disposition. Manage the CAPA system to ensure that corrective and preventative actions are made and followed
- Perform cGMP audits within functional areas by conducting a thorough review of processes and documentation. Identify and communicate cGMP compliance deficiencies to Management Team, recommend appropriate corrective actions when necessary, and perform necessary follow up with respective functional area management to ensure cGMP audit observations are implemented
- Provide support to functional areas regarding the Change Control System by providing assessments, work closure, and follow-up. Recommend documentation and supporting data to include in the Change Control Request to ensure that enough information is provided to so that an informed decision can be made
- Promote a highly safety conscious culture and EHS focused workforce
- Represent QA on key forums and teams to evaluate and provide QA recommendations on products, systems, and issues that are affected or may be affected by regulatory or cGMP requirements for any proposed changes or new information
- Perform all job responsibilities in compliance with applicable regulations, current operating procedures and industry practice
- Participate in investigations of escalations, lead the investigation report preparations and follow up all necessary actions
- Prepare annual site Self-Inspection plan and ensure activities are completed on-time
- Maintain document control system (issuing, reviewing, updating and canceling) for all company processes including Standard Operating Procedures (SOPs) and Master Production Batch Records
- Identify key manufacturing risks across different functions and devise mechanisms to mitigate them
- Drive investigations of Critical Deviations & Complaints as a member of Quality Compliance team and provide guidance on related topics

**B. Job Requirements**:

- Bachelor’s degree in science or related discipline (e.g. Chemistry, Pharmacy, etc)
- Professional knowledge and experience of GMP and Total Quality Management System
- Strong verbal and written communication skills
- Strong analytical and problem-solving skills
- Proficient to advanced Microsoft Excel skills; Microsoft Access skills a plus
- **At least 8-10 years of experience in Pharmaceutical, Biopharmaceutical or related manufacturing environment, in which at least 3 year in Quality Compliance Managerial

**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

Your Role Responsibilities:
Analyzing users stories and/use cases/requirements for validity and feasibility

Collaborate closely with other team members and departments
- Execute all levels of testing (System, Integration, and Regression)
- Design and develop automation scripts when needed
- Detect and track software defects and inconsistencies
- Provide timely solutions
- Provide support and documentation

Your Role 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

Pay: E£17,171.42 per month

Lead the Quality Assurance function thereby ensuring that all processes and procedures, tasks, responsibilities and projects are in compliance with all pharmaceutical laws, Quality Manual and Policies as well as Industry Best Practices.
- Comprise special GxP requirements.
- Ensure that all quality relevant processes are compliant and that non-compliance is appropriately addressed via corrective & preventive actions (CAPA) and/or escalation of issues
- Ensure implementation of applicable Quality Standards and governance processes and all regulatory controls are in place in relevant process steps
- Ensure adherence to GxP, any further legal and company internal regulations for manufacturing, control and distribution operations and to HSE guidelines and requirements
- Ensure implementation of defined Key Quality Indicators in the area of responsibility to monitor on an on-going basis that relevant processes are in control and compliant. -Ensure regularly review and assessment of KQIs at the Leadership Team level.
- Ensure adequate escalation of issues and support their timely resolution & provide quality oversight for deviations and adequate corrective and preventive actions (CAPA’s) are implemented.
- Provide quality oversight for planned changes.
- Adequate regulatory inspection preparation, management and follow-up in the area of responsibility.
- Communication with local Health Authorities is adequately shared within the organization and commitments tracked and closed on time.
- Implementation of adequate training within the area of responsibility for all GXP activities by defining, planning and supporting training activities.
- Ensure that processes are in place to communicate country specific requirements to the Region and headquarter organizations for all GXP areas and assess their implications for the compliance of existing processes and systems.
- Initiate remediation activities, as necessary, to ensure ongoing compliance.
- Adequate processing of complaints.

**Commitment to Diversity & Inclusion**:

- Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve._

**Minimum requirements**
- University degree
- Extensive experience in Operation Management and Execution with people management experience
- Sustained Performance & Behavior
- Good understanding of country, regional and local dynamics
- Demonstrated ability to think broadly and innovate within the Pharmaceutical business
- Working knowledge of Pharmaceutical procedures and trends

**Division**
- SANDOZ

**Business Unit**
- Commercial OPS SIR SZ

**Country**
- Egypt

**Work Location**
- Cairo

**Company/Legal Entity**
- HEXAL EGY

**Functional Area**
- Quality

**Job Type**
- Full Time

**Employment Type**
- Regular

**Shift Work**
- No

**Early Talent**
- No

Be part of something bigger. Decode the future.

At Electrolux, a leading global appliance company, we strive every day to shape living for the better for our consumers, our people and our planet. We share ideas and collaborate so that together, we can develop solutions that deliver enjoyable and sustainable living.

Come join us as you are. We believe diverse perspectives make us stronger and more innovative. In our global community of people from 100+ countries, we listen to each other, actively contribute, and grow together.

Join us in our exciting quest to build the future home.

What you'll do:
The position is responsible for ensuring that a company's products and processes meet established quality standards by identifying shortfalls, developing corrective measures, and implementing quality control systems.

**In detail, you will**:

- Responsible for process and system quality audits against all standards.
- Ensure adherence to the Quality management system.
- Analyze Quality data coming from customer feedback, product control and capability analysis.
- Create and follow-up actions related to continuous improvement in relation of the KPIs results and analysis.
- Work closely with the manufacturing team to create and update FMEA.
- Establishing the required action plans to improve final product & customer returns KPIs
- Implement the requirement of quality management system ISO 9001-2015.
- Generate & create ideas and techniques for continuous improvement related to this area of interest to minimize the cost of processing or inspection.

Qualifications:

- Bachelor’s degree engineering, (Mechanical/Mechatronics are preferred)
- Experience: 0-3 years of experience in quality and preferred with industrial quality.
- Fluent Spoken and written command of English language.
- Strong Logical and analytical thinking.
- Problem solving skills through innovation and creativity

Where you'll be:
You will be based at Electrolux Manufacturing Site at 10th of Ramadan City
- Sharkia Governate
- Egypt.

As part of Electrolux, we will continuously invest in you and your development. There are no barriers to where your career could take you.

Find out more on:
Electrolux Group

(#LI-SS3)

**Duties and Responsibilities**:

- Responsible for calibrating, monitoring, and supporting the quality standards between internal and external parties.
- Create process documentation/workflows/Work instructions, knowledge articles, and self-service guidance.
- Collect and document business requirements for project and process improvement/automation efforts.
- Perform an internal audit to make sure that all departments are working by the officially agreed process.
- Facilitate process workflow modeling to collaborate on process improvements, automation capabilities, and clearly defined end-to-end use cases.
- Review information and trends to ensure that the output of processes achieves the desired results and that services meet agreed service levels.
- Conduct maturity assessments against the process activities to highlight areas of improvement or concerns.
- Identify issues and risks.
- Bring inconsistencies and problems to the attention of management.
- Participate in solving problems.
- Track major incidents and ensure adherence to the process and escalation of requirements within the various support and delivery areas.
- Extract reports and provide a high-level analysis of data for review.
- Participate in the planning of QA department objectives.
- Manage and improve the quality control process.
- Set goals and metrics, and report on quality control results continuously.
- Communicate quality concerns with stakeholders.
- Developing test plans and test cases to ensure that our services meet quality standards.
- Working with cross-functional teams to ensure that quality is built into the product development process.
- Investigating and resolving any quality-related issues that arise.
- Continuously improving the QA process to ensure that it is effective and efficient.

**Skills/Qualifications**:

- Previous working experience in the localization industry minimum of 2 years is preferable.
- Previous working experience as a Quality Specialist minimum of 2 years.
- Working knowledge of tools, methods, and concepts of quality assurance.
- Bachelors in business administration, computer science, or a similar relevant field.
- Excellent organizational and time management skills.
- Outstanding communication and presentation skills.
- Critical thinker & self-motivated.
- Creative problem solver.
- Great analytical skills.
- Data-driven approach.
- Excellent in MS Office, Adobe Acrobat, and PowerPoint (many reports and presentations will be required)
- Fluent in English.
- Strong Leadership and Communication skills.
- Knowledge of ISO 9001:2015 & ISO 17100:2015 is preferable.
- Background localization & translation industry is preferable.

**RESPONSIBILITIES/DUTIES**: This includes but is not limited to:

- In the context of complex automotive projects with multiple teams working in parallel, manage the quality of the intermediate and final deliveries (inter-team deliveries and customer deliveries).
- Execute both random inspections and planned audits on different work products in the project.
- Identify and evaluate quality metrics and present them to management and customers.
- Proactively support project managers to plan corrective actions to improve quality.
- Execute different quality audits on selected projects inside the organization.

**REQUIREMENTS**:

- Bachelor’s degree in Electronic Engineering /Computer Engineering /Computer Science or equivalent combination of education/experience.
- 3+ years of hands-on experience in the Software Quality Assurance / Software Development field.
- Strong knowledge of Agile, CMMI, ASPICE 3.1, and ISO26262.
- Experience with the Software development process, Systems engineering methodologies, and test techniques.
- Ability to troubleshoot issues to resolution. Strong problem solving and root cause analysis skills.
- Capability to enforce discipline and process compliance within complex project environments.
- Excellent communication and negotiation skills with other teams and the customer.
- Very good English language (spoken and written) is required.

**Job Features**:

- Job Category- Embedded

**NAOS Talents **is looking to hire a **Senior Quality Assurance Specialist **for **a leading global car-sharing company.**
- **Objectives of this Role**:

- Interpret, build upon, and comply with company quality assurance standards.
- Carefully maintain a complaint and nonconformance processing through records. and tracking systems, including root causes and corrective actions.
- Document quality assurance activities with internal reporting and audits.
- Develop new standards for service with improvements as needed and create testing protocols for implementation across all service lines.
- Identify training needs and take action to ensure company-wide compliance.
- **Daily and Monthly Responsibilities**:

- Providing high-quality car and driver services meeting customer needs in car rental services and providing them with quality services.
- Preparing and implementing quality assurance policies and procedures.
- Performing routine inspections and quality tests.
- Plan, execute, and oversee inspection and testing of services to confirm quality conformance to specifications and deliverables.
- Assist operations in tracking, documenting, and reporting quality issues.
- Analyze and investigate customers' complaints or reported quality issues to ensure closure following company policies and procedures.
- Documenting quality assurance activities and creating audit reports.
- Seek customer satisfaction, taking into account their requirements.
- Making recommendations for improvement.
- Increase customer satisfaction by managing Google Customer Reviews and company ratings on RentalCars.
- Identification of measures for a sustainable increase in customer satisfaction and service quality and to reduce customer complaints.
- Develop or update company inspection procedures to ensure capture and investigation, as well as proper documentation of complaints.
- Analyzing problem logs to identify and report recurring issues to the quality manager.
- Addressing and discussing issues and proposed solutions with the quality manager

**Education, Skills & Qualifications**:

- Bachelor’s degree in any related field.
- Years of Experience**: 4 - 6 Years of experience**
- Valid driver’s license.
- Work under mínimal supervision and have excellent time management skills.
- Professional certification, such as **Six Sigma or Quality Auditor.**:

- Superb computer competence, including database management.
- Knowledge of quality assurance terminology, methods, and tools.
- Analytical, problem-solving, and decision-making skills.
- Good communication skills, both verbal and written.
- Strong attention to detail.
- Background in customer experience management.
- Excellent written and verbal communication skills in English.
- Demonstrated knowledge of testing best practices, version control practices, and defect management practices.

**Salary and Benefits**:

- Gross Salary Range**:9,000 - 13,000 LE**
- Bonus Scheme: 1 Month bonus based on evaluation - Paid quarterly
- Medical Insurance Coverage
- Social Insurance