9 Site Supervision jobs in Egypt

3803 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 (QC Finished Products Analyst) role will make an impact:

- Position summary:

- Conduct routine and non-routine analyses and relevant documentation and reporting.
- Performance of lab-related tasks.

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 Viatris Policies’ 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.
- cGMP & cGLP knowledge is preferred with particular emphasis on Quality Control.
- Knowledgeable with basic Laboratory instruments such as pH, Spectrophotometry, HPLC and reagent preparation.
- Responsible for ensuring that all results generated follow data integrity requirements.
- Responsible for raising “NTM” Notification to Management whenever condition in Viatris policies applies.

The Minimum Qualifications for this role include:

- Bachelor’s degree in Pharmacy or Science.
- 1-2 years’ experience in a related area.
- Good command of English in both written and spoken.
- Excellent in Microsoft office (word, excel & PowerPoint)
- Knowledgeable with interpersonal, good communication and presentation skills.
- cGMP & cGLP knowledge is preferred with particular emphasis on Quality Control.
- Knowledgeable with Laboratory instruments such as pH, Spectrophotometry, HPLC and reagent preparation.
- Demonstrated ability to work independently.
- Must be able to work in a stressful, on-demand environment and be able to communicate under stress in a non-confrontational, effective manner.
- Excellent documentation and technical writing skills.
- Able to work in a team, interact with various priorities and meet deadlines.
- Active, organized and planner with high attention to details.
- High observation skills.
- Hard worker & self-motivated.

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.

**Job Description**:

- Conducting quality checks on all input materials from providers as well as existing items for distribution regularly.
- Discarding any products or materials that do not meet quality standards.
- Performing inventory checks and keeping quality standards high for audits.
- Keeping a clean and safe working environment & ensure the adherence of all staff members to health & safety policies/regulations.
- Completing diary logs into inventory.
- Reporting any discrepancies & controlling risks & incidents.
- Communicating and cooperating with supervisors and coworkers.
- Ensure the safety & efficiency of warehouse vehicles and equipment.
- Maintaining and organizing all records, documentation, and other files associated with quality & inspection processes.

Qualifications:

- Bachelor's degree is a must.
- 1-3 years of proven experience as a quality officer in warehousing preferably infood Safety Protocols.
- Very Good command of English.
- Strong working knowledge of warehouse operations and management
- Proficiency in Microsoft Office and data entry software

**Job Purpose**:
Responsible for performing basic tasks and some standardized routine testing and maintaining a high level of quality sections services by monitoring and recommending solutions to quality related issues under close supervision.
- Performs wet and instrumental analysis (HPLC, UV, GC, FTIR) of raw materials, in-process and finished products.
- Performs physical testing and chemical analysis of Pharmaceutical Packaging Material.
- Troubleshoots and resolves operations issues.
- Prepares and standardizes volumetric solutions, reagents and indicators Internal calibration of instruments according to work instructions.
- Validation of the assay methods of finished products.
- Participates in validation of facilities and manufacturing processes

**Qualifications**:

- Bachelor’s degree in Pharmacy or Science with grade Very good.
- Minimum Experience: 1-2 years of experience in same field
- Fluency in English, both written and verbal
- V. Good computer skills and data analysis knowledge.
- Good documentation practices and technical writing

RESPONSIBILITIES
- Review project’s specifications of the project and the contractual drawings.
- Prepare the inspection and hand over requests in coordination with the construction team after making sure that the work is ready to be handed over to the consultant.
- Hand over the implemented work to the project’s consultant after ensuring its compatibility with the project’s specifications.
- Participate in the inspection committees of the materials supplied to the project to accept or reject the materials according to the project’s specifications.
- Report cases of non-conformity of works, which do not conform to the contractual specifications according to the company's quality procedures and follow-up the necessary corrective actions towards closing those cases.
- Prepare and approve work implementation processes in partnership with the construction team and the technical office team.
- Coordinate with the consultant in approving the tests’ results and experiments carried out in the project laboratory or external laboratories.
- Follow-up the tasks that are assigned to the quality control engineers.
- Prepare monthly quality reports for the project, including inspection and handover requests and non-conformity cases sent by the consultant, and take the necessary corrective measures to close non-conformity cases in coordination with the project management.
- Attend regular meetings when needed and represent the quality department with the consultant and the client.
- Participate in the internal reviews that are carried out in the company in coordination with the project management and the quality control department in the head office.
- Follow the health safety instructions in the site and make sure of knowing the duties during evacuation and emergency plans.

QUALIFICATION

BSc. of Engineering

REQUIRED EXPERIENCES

8 - 12 years of experience

Company Description
**Homzmart** is an end to end community that connects home professionals with homeowners who can browse home designs, furniture, accessories and products and also can find reviews, referring professionals, take advice from professionals and read articles about home improvement.

**Job Description**:

- Responsible for individual contribution to test cases based on release content and
- Marketing Requirements and perform a test.
- Design and execute test cases and test scenarios.
- Review requirements documents in terms of consistency, completeness, and
- correctness.
- Verify that implemented software meets the business requirements.
- Perform functional and UI testing for new or modified features based on quality and usability standards
- Execute test cases and test scripts on the system.
- Record and document results and compare to expected results.
- Suggest functionality improvements based on usability standards
- Provide guidance and support to Software Quality Engineers
- Communicate with the Quality Lead to discuss projects issues and schedule.
- Communicate with the Quality Lead on performance issues.
- Ability to understand new testing techniques, technologies, and tools
- 6+ months of hands-on Automation Testing is a plus.

**Qualifications**:

- 1+ years of hands-on experience in software testing.
- Good understanding of the software development and testing process.
- Good knowledge of software testing types and techniques.
- Experienced with agile concepts and hand-on experience in agile testing.
- Experienced with Test Management tools (Zephyr, or& Xray) preferable
- SQL Scripting Knowledge in one or more enterprise RDBMSs (MYSQL, or& Oracle).
- Analytical and creative problem-solving skills.
- Performance testing Knowledge is a plus.
- Very Good command of the English language.
- Ability to understand new testing techniques, technologies, and tools
- 6+ months of hands-on Automation Testing is a plus.

Job Purpose:
The main purpose of this job is to perform chemical analysis for validation samples for products according to the approved method of analysis, and prepare relevant documentation as required.- Perform analytical method validation studies, Protocols & final reports.- Perform recovery studies & prepare cleaning validation & verification runs.

Responsibilities and Tasks:
1- Performs all physicochemical testing of samples collected during the process validation and record the results in the validation report & Certificates of analysis required and ensures that all obtained results are within the specified approved limit, using valid method of analysis.

2- Performs the analytical transfer analysis according to respective protocol.

3- Perform coaching and training for junior analyst for the Analytical method validation and explain the methodology and ensure that all the junior analyst (s) understand the method validation concept and can perform full study independently.

3- Immediate reporting of out of specification test results or batch deviation reports whenever needed to the Q.C manager.

4- Perform analytical full method validation studies, Protocols & final reports.

5- Updating of SOPs & control test methods and maintaining of relevant master files.

6- Performs Standardization for Raw Materials

7- Perform Stability testing & routine analysis tasks If assigned.

8- Perform recovery studies & prepare cleaning validation & verification runs.

9- HSE & Energy Contribution:
Ensures HSE approval on any SOP that requires certain HSE precautions. Ensures HSE approval on any change. Follow the laboratory safety procedures 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. Implement good calibration program for all instruments.

Supplementary Tasks:
Utilizes, calibrates, maintains the QC equipment in the Chemical Lab according to the local SOP.

Prepares relevant SOPs and follows up the update according to requirements.

Perform other related duties as assigned.

Makes sure that all activities carried on are complying with safety measurements.

Updates methods of analysis.

Respect of Company’s Values, Code of Ethics and Social Charter.

Respect Personal Data Protection Charter.
- 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, disability, or gender identity.
- Watch our
- ALL IN video
and check out our Diversity Equity and Inclusion actions at

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

**Employment Type**

**Rank Requested**

**Gender**

**Location**
- Egypt

**City**
- Cairo

**Residence**
- Heliopolis

**Salary**
- Negotiable / month

**Transportation**
- / month

**Benefits**
- social, Medical insurance, bonus

**Working hours**
- From 0 To 0

**Days off**
- 0

**Requirments**

**Age**
- From 0 To 0 Year(s)

**Computer Skills**

**Years of experience**
- Min 5 Max 8 Year(s)

**Car**
- Any

**Woman's Veild**
- Any
- 1. Inspect works on site and coordinate with project and consultant the daily inspection process
2. Prepare, update and follow up the non
- conformance reports and the corrective & preventive actions taken
3. Check on daily basis the materials delivered to site are according to submittals and project specs
4. Prepare & following up snagging list for the finished buildings and zones to be ready for clients handing over
6. Audit and checking with document controllers the various logs (IR (Inspection Request) -MIR (material inspection request) -SWI (site work instruction) -NCR (non
- conformance report) )
7. Review and audit the test results of the labs (concrete tests
- soil tests - several materials)
8. Check the pouring activities on site are according to the approved mix design and the project spec.

Position: Quality Control Manager (Large Group)

Location: Cairo, Egypt

Contract Details: Full-time, 5-year contract

Company Overview:

Our company is a large group with a diverse portfolio of businesses, including manufacturing, distribution, and retail. We are committed to providing high-quality products and services to our customers and maintaining a strong reputation in the market. As we continue to grow and expand, we are looking for a Quality Control Manager to join our team in Cairo, Egypt.

Job Overview:

As the Quality Control Manager, you will be responsible for overseeing the quality control processes and procedures for all of our businesses in Cairo, Egypt. You will work closely with department managers and employees to ensure that our products and services meet or exceed industry standards and customer expectations. This is a full-time position with a 5-year contract.

Key Responsibilities:

• Develop and implement quality control policies and procedures for all departments within the company.
• Monitor and evaluate the quality of products and services throughout the production and distribution processes.
• Conduct regular inspections and audits to ensure compliance with quality standards.
• Identify areas for improvement and make recommendations for process enhancements.
• Train and educate employees on quality control processes and procedures.
• Investigate and resolve any quality-related issues or complaints from customers.
• Stay up-to-date with industry standards and regulations to ensure compliance.
• Collaborate with suppliers and vendors to maintain quality standards for raw materials and components.
• Manage a team of quality control inspectors and provide guidance and support as needed.

Qualifications:

Job Holder Technical Skills:

• Bachelors degree or similar in Quality Management, Science or Engineering
• 10-15 years of quality management experience within Food Production Manufacturing Especially Coffee, Pulses & Grains Production.
• Knowledge of ISO & NAFSA quality standards and experience performing quality and food safety system audits
• Professionalism and dedication to excellence in quality and customer care
• Excellent relationship building skills and communication
• Proven track of leading people and passion to develop employees
• Highly self-motivated and self-driven
• Profound MS Office skills
• Available to Reallocate to Gamasa.
• Experience with ERP (SAP/ORACLE).

Personal Competencies:

• § Communicative, committed, flexible, with excellent professional standards.
• § Reliable, accurate, with attention to detail.
• § Excellent Arabic and English skills.

.

If you are a highly motivated and experienced Quality Control Manager looking for a new challenge, we would love to hear from you. Apply now to join our team in Cairo, Egypt and help us maintain our commitment to quality and excellence.