8 Manufacturing Inspector jobs in Egypt

Job Summary: The Quality Control Engineer’s main objective is to monitor software quality and the technical risks associated with the software development lifecycle.

Job Responsibilities:

- Design and maintain test cases and strategies for cross-browser testing and multiple user scenarios.
- Satisfy release deliverables, project testing requirements and other quality assurance responsibilities.
- Collaborate with the team to understand product changes and testing requirements to deal with issues/defects in a timely manner.
- Establish a testing feedback loop with other developers and team members.
- Debug test environment, and develop testing scenarios.
- Hands-on experience with API Testing using Postman

**Requirements**:

- Bachelor degree in computer science, software engineering or a related field.
- Experience in mobile Apps (Android-IOS), and web testing
- Good knowledge of software QA methodologies, testing types, tools, and processes.
- Preferable to have previous experience in JIRA
- Excellent written and verbal communication skills.
- Excellent written and spoken in both English and Arabic.
- Certificated (ISTQB) Foundation level is a plus.

**Benefits**
- Social and Medical Insurance are provided
- Working in agile environment
- Career growth and development

**About the job Quality Control Engineer**:
Skils and requirements:

- Review and analyze requirements, specifications, and technical design documents, providing timely feedback.
- Develop detatled, comprehensive, and well-structured test plans and test cases.
- Prioritize and plan testing activities.


- Play the role of test engineer: Design, develop, and execute automated tests.
- Identify and report issues found, then verify that issues are resolved.
- Perform regression testing.
- Technical Skills:

- Proven work experience in software quality assurance.
- Strong knowledge of software QA methodologies, tools, and processes.
- Hands-on experience with automated testing tools.
- 1-2 years of Hands-on experience with Selenium and CH.
- Keen eye for detail and a commitment to excellence.
- Be willing to help your teammates, share your knowledge with them, and learn from
Then.
- Be open to receiving constructive feedback and turning it into process improvements.
- Good command of English language.

Viatris Egypt S.A.E

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

Viatris empowers people worldwide to live healthier at every stage of life.

We do so via:
Access - Providing high quality trusted medicines regardless of geography or circumstance;
Leadership - Advancing sustainable operations and innovative solutions to improve patient health; and

Partnership - Leveraging our collective expertise to connect people to products and services.

Every day, we rise to the challenge to make a difference and here’s how the “Quality Control Analyst” role will make an impact:
Key responsibilities for this role include:

- Conduct routine and non-routine analyses of in-process materials, finished goods, or stability samples

in a timely manner.
- Interpret test results, compare them to established specifications and control limits, and make

recommendations on appropriateness of data for release.
- Conduct chemical or physical laboratory tests in making qualitative or quantitative analyses
- Complete documentation needed to support testing procedures including data capture forms,

equipment logbooks, or inventory forms.
- Write technical reports or prepare graphs or charts to document experimental results.
- Calibrate, validate, or maintain laboratory equipment.
- Participate in out-of-specification and failure investigations and recommend corrective actions.
- Supply quality control data necessary for regulatory submissions.
- Investigate or report questionable test results.
- Addition and withdrawal of stability samples from stability chambers
- Performance of data entry and trend analysis
- Reviewing, filing, reporting and trending of stability data
- Perform the Analytical Method Transfer Exercise (AMTE) for the new test procedures required for

manufacturing of new product in our site.
- Perform Validation required for the new developed test procedures.
- Execute all activities related to process, cleaning and instrument validation.
- Preparing and executing the SOPs, calibration and validation documents (IQ, OQ & PQ) related to

chemical laboratory tasks.
- Implementing the PQS requirements regarding the chemical laboratory
- Using, monitoring and controlling Reference standards inventory and expiry
- Using, monitoring and controlling of expiry and inventory of laboratory stock items including reagents,

glassware, filters, etc.
- Perform Data loggers monitoring, downloading and reviewing
- Writing and revision of Quality Control SOP’s
- Working on improving his process by implementing lean and 6σ projects.
- Responsibility for implementation of Data integrity program in the relevant work area and Insure

following up ALCOA principles all over operations.
- Active implementation of Notification to Management procedures.
- Responsibility for compliance with Viatris Quality Standards.

The minimum qualifications for this role are:

- BSC in Pharmaceutical / Chemical science.
- 1-3 years of experience in Quality Control Laboratories.

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer.

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 +20 years of prominent existence in the local market and has almost +66 products marketed and more to come through the pipelines. Multicare Egypt for Pharmaceutical Industries is the manufacturing facility of Pharmacare for Trading Agency, which located at the Industrial Zone - New Cairo and its HQ is close by the facility 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.

**VACANCY**:
We are recruiting professional caliber to join the team as per the following details:
**Designation**: Microbiology Supervisor
**Location**: Multicare For Pharmaceutical Industries Manufacturing Site - The Industrial Zone, 03rd Settlement, New Cairo ( Kattamia)
**Reporting**: Microbiology Section Head
**Grade**: FQ01/FQ03

**Job Purpose**:
This position is centered on the supervision of the QC Microbiology & Environmental Monitoring to ensure effective and efficient laboratory testing is performed by support staff while simultaneously ensuring compliance to pharmaceutical regulations, safety standards, and environmental policies

**A. ESSENTIAL DUTIES and RESPONSIBILITIES**:

- Manage the Microbiology Laboratory ensuring that the equipment is functional (calibrated and well maintained) and suitable for analytical testing
- Handle workload and resources to ensure timely release of product. Manage the sampling and analysis of raw materials, intermediates, finished products, routine monitoring samples and others.
- Ensure that testing is carried out in compliance with specifications, Pharmacopoeia requirements and the cGMP and analyze the trend of the analytical results. Ensure the OOS investigation is conducted properly
- Ensure that Reference Standards as well as Standard Solutions are suitable and maintained according to the cGMP. Maintain and control the inventory of test material and consumables, including toxic reagents, ensuring that the budget is respected
- Release the Raw materials, Packaging materials and Semi-product(Imported) according to the test results
- Implement GAP analysis for global requirement and local authority standard and take CAPA actions
- Identify significant adverse quality trends by preparing and analyzing summary reports and key process indicators. Addresses quality control test results, microbial profiles of environmental areas, and customer complaints
- Keep close relationship and communication with other departments to ensure proper execution of the production plan. Lead and motivate the analysts for a continuous improvement of GMPs as well as HSE awareness. Be the Safety contact for the Laboratories
- Assist QC Section Head in planning and prioritizing resources allocation to meet test requirements. Responsible for training staff and overseeing and reviewing documentation
- Lead microbiological analysis of raw materials and finished products, environmental monitoring, water analysis, reviving of pathogenic microorganisms and different microbiological studies
- Ensure L1 Self Inspection procedures for area of responsibility are in place and in use
- Revise/update/draft Standard Operating Procedures (SOPs) governing the departmental activities
- Responsible for interdepartmental interactions to ensure customer service needs are satisfied and priorities understood
- Generate trend reports as they relate to quality testing
- Ensure sample submission for external testing
- Perform visual inspection of finished product, as needed
- Interact with internal departments, including Production, Facilities, Quality Assurance, Validation, Calibration, Materials, and Logistics as needed
- Ensure that an adequate supply of inventory levels is maintained
- Ensure that all documentation is neat and orderly and maintain all necessary documentation
- Conduct special studies as required and maintain inventory control
- Identify and implement issues and opportunities for improvements driven by continuous improvement inclination
- Supervise the collection and evaluation of incident report and change control data and ensures the necessary corrective actions are identified and implemented. Reviews and evaluates mont

**Responsibilities**:

- Send 8 D reports to the Suppliers regarding nonconforming material. Follows-up on corrective action to ensure continuous improvement.
- Evaluates the supplier performances.
- Preparing Suppliers complaint cost.
- Update FMEA.
- Close the processes concerning the quality on company related system tools.
- Creating Equipment check list approval.
- Perform statistical analysis, MSA (Pareto chart, R&R, MFU).
- Preparing Monthly Quality Reports.
- Evaluate 6S activities.
- Monitoring ultrasonic daily check records.
- Conduct Error proofing Audit.
- Investigating and troubleshooting production or product errors
- Conduct System Audits according to QMS.
- Submit the quality reports to the QC Manager.
- Perform all other duties and tasks as assigned.

**Job Requirements**:

- Must have Degree in mechanical engineering, in quality or industrial engineering.
- 2-3 years of experience in quality engineering.
- Strong communication and interpersonal skills.
- Strong analytical and problem-solving skills.
- Advanced communication and language capabilities (written and verbal)
- Excellent MS office, advanced excel is preferred
- Deal with PDF programs, AutoCAD knowledge is preferred
- Excellent written and spoken English is a must.
- IATF 16949 knowledge is a plus
- Organized and stick to the plan
- Ability to handle intersected plans
- 6th of October residence is preferred
- Giza Residence is a must, 6thof October is preferred

**Work location**:Giza, 6th of October

If you are interested, please send your C.V to:
**Salary**: From E£1,111.00 per month

Ability to commute/relocate:

- 6th of October City: Reliably commute or planning to relocate before starting work (required)

Application Question(s):

- Are you a Giza residence?

**Education**:

- Bachelor's (required)

**Experience**:

- Quality Control: 2 years (required)

**Language**:

- English on a daily basis (required)

**Summary**

**Responsibilities**
- Design and develop test cases for software tools and websites to verify product functionality according to user requirements
- Write clear and concise bug reports and scenarios to ensure clear communication with the software developer
- Approve updates to the software tools and websites while ensuring product efficiency
- Maintain and manage manual and automated scripts and test databases
- Write complex SQL queries for data retrieval
- Test software releases by executing assigned tests (manual and/or automated)
- Test web services and APIs
- Support the team with testing tasks as required
- Follow up with junior software testers and reporting status to the team leader
- Report overall project status and generating statistics

**Qualifications & Work Experience**
- Bachelor’s degree in a related field, computer science background is preferred
- 3-5 years of experience of relevant experience
- Good mobile testing experience
- Excellent command of the English language
- ISTQB certification is a must
- Previous working experience as a software developer for at least one year is preferable
- Previous working experience involving agile Scrum
- Proven experience in at least one of the following areas of testing: automation, performance, security

**Behavioural Competencies**
- Outstanding research skills
- Very good communication skills
- Attention to detail
- Time and stress management skills
- Problem-solving skills
- Adaptability and flexibility
- Analytical thinking skills

**Benefits**
- Private medical insurance
- Flexible working hours
- Learning and educational leaves
- Transportation service
- Special benefits for new mums and dads (Leaves & Nursery subscription)
- Lunch break, food services and fun & games area

2OnRxSRhLR

**Company Description**
Established in 1989, ABEC was restructured in 2020 to deliver innovative buildings efficiently and provide full integrated construction service. The company had a wide history of construction projects in various industries in the past, which now decided to take a different route focusing on specific types of buildings.
- Create, update and maintain the project submittal log and all other project-specific quality control reports
- Provide written daily QC reports that reinforce activities that are being constructed in conformance with each specific project's established standard and constructively confront non-conformances to produce the desired outcome in a timely manner
- Implement the QC management system at the site
- Coordinate quality inspections with all the site staff
- Prepares reports by collecting, analyzing, and summarizing data; making recommendations
- Verify and document that all materials received for the project are in conformance with the approved submittal, are handled and stored appropriately, and are acceptable for use in the project
- Conduct preconstruction meetings with new and existing subcontractors and the superintendent at least two days prior to the start of each new phase of the work to discuss issues that affect quality. Document these meetings in the daily QC report and Preparatory Phase reports
- Schedule, document the results of, and maintain a log of all code and independent inspections that are required. Clearly document, correct, and re-inspect all non-conformances prior to covering up work
- Document final inspections, certificates of occupancy, and acceptance of the works and various phases thereof
- Maintain the project "as-built" drawings.
- Coordinate all types of testing on site
- Coordinate with the customers’ representative on all quality matters
- Coordinate all receipt inspections
- Monitor and Implementation of document controlling system and other procedures
- Distribute relevant QC documentation to site subcontractors
- Verify that the quality-related site activities are in accordance with the applicable codes and standards
- Participate in the site’s internal and external site audits
- Devises sampling procedures and designs and develops forms and instructions for recording, evaluating, and reporting quality and reliability data.
- Assist QC Manager in conducting internal quality audits.
- Provide technical support to the Project Manager and guidance to site staff in the submission of materials for approval, request for inspection, and shop drawings.
- Liaise with the Client's representatives for the conduct of day-to-day quality-related project activities.
- Conduct periodic follow-up inspections to verify that work is proceeding with the contract documents and the approved submittals. (Desired results come from what is inspected, not what is expected.)
- Stop work if necessary to resolve matters that affect safety, quality, and/or inhibit the logical progression of work

**Qualifications**
- Bachelor in Civil Engineering.
- Minimum Required Professional Experience
- from 3:7 years of experience in quality control & quality assurance programs of similar size and type.