8 Pharmaceutical Industry jobs in Egypt

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**Quality Control Analyst**:
Egypt

**About the role**

Location: Cairo, Egypt #LI-Hybrid
About the Role:
As a Quality Control Analyst, you will be responsible for conducting routine analysis of products in accordance with approved specifications, testing monographs and standard operating procedures using a wide spectrum of chemical techniques and equipment.
This role reports directly into the Analytical Science and Technology Head.
Key Responsibilities:

- Implement health and safety procedures as required (Novartis HSE Requirements).
- Execute all required analytical procedures in compliance with cGMP/organizational standards.
- Implement the required working knowledge of analytical techniques, specialist knowledge and others to support cGMP/organizational standards.
- Minimize/ eliminate own cost of non-conformance, OOSs and deviations (with laboratory root causes), assist with the analysis of incidence to prevent recurrence, and guide associated team members to the same goal.
- Create and review QC standard operating procedures to ensure maintaining compliance with cGMP.

**Commitment to Diversity & Inclusion**:

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

**Role Requirements**

Essential Requirements:

- BSC in Pharmaceutical / Chemical science.
- Fluency in Arabic and sound command of spoken and written English.
- Previous experience in laboratory analyses is a must.

Desirable Requirements:

- Experience in planning for resources usage.

Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here:

You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook.

Commitment to Diversity and Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
Novartis is a proud member of the ILO Global Business and Disability Network and the Valuable 500, promoting the inclusion of people with disabilities in workplaces around the world. We also collaborate with international partners, such as Disability: IN, Purple Space, and Business Disability Forum to identify and develop best practice solutions to enable people with disabilities to participate as equal members of our organization.

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here:
**Division**

Operations

**Business Unit**

QUALITY

**Work Location**

Cairo

**Company/Legal Entity**

NOV PHARMA EGY

**Functional Area**

Quality

**Job Type**

Full Time

**Employment Type**

Regular

**Shift Work**

No

**Early Talent**

Yes

**Purpose of the job**

**Accountabilities and Duties**
- Review requirements to ensure they are clear, valid, and testable and to ensure that there is no ambiguity or contradictions.
- Developing and reviewing manual test cases in a descriptive, structured, and understandable way.
- Ensuring the proper execution of test cases and reporting their results.
- Logging issues in a clear and accurate way on the bug tracking tool (Jira) and tracking them until closure.
- Responsible for ensuring the commitment of predefined testing schedules.
- Reporting test cases and issues status to Quality Control Manager.
- Defining and executing regression sets and reporting the execution progress
- Creating Estimations and Test Schedule plan for tasks assigned.
- Responsible for handling the communication with development team.
- Helping in troubleshooting issues and should be able to identify the root cause of any issue.
- Responsible for following the company quality standards & processes.
- Creating UAT test cases for the client to deliver with high quality.
- Coaching Associates and Software Quality control members and helping them achieve their objectives.

**Key Results Areas**
- Proper tests as per the process
- Final reports with high quality
- On-time reporting and feedback
- Accurate follow up on logged issues and bugs
- Coaching and following up on QC members and associates

**Experience and Qualifications Required**:

- Bachelor degree in Engineering, Computer Science, or equivalent.
- Minimum 8+ years of experience in testing of similar software.
- Excellent command in using testing techniques (functional and non-functional).
- Good knowledge of SQL database administration
- Working experience with test management tools: Jira, HP ALM, etc.
- Experience in any functional test automation tool is preferred.
- Solid experience in agile methodologies
- ISTQB foundation level certificate is a must.
- ISTQB Foundation Level Agile Tester is a must.
- ISTQB foundation level Mobile Application Testing is a must **FOR PRINCIPAL ONLY.**:

- CP-SAT Certified Professional Selenium Automation Testing is a must.
- Knowledgeable about API.
- Excellent English language is a must.

**Competencies Required**:

- Communication
- Analytical thinking
- Diagnostic Information Gathering
- Technical Expertise
- Workload management
- Quality Oriented

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 (Senior QC Analyst ) role will make an impact:

- Key responsibilities for this role include:

- A - Identification Task:

- Purify isolates to single colonies using appropriate media and incubation conditions.
- Prepare and read wet mounts, Gram stains and Spore stains.
- Perform preliminary and confirmatory tests for the identification of microorganisms.
- Prepare Vitek cards for identification. Report and interpret results.
- Maintain the departmental culture collection.
- Perform identification of mould isolates.
- Proper completion and review of associated logbooks.
- Complete prompt and timely investigations of any irregularities concerning isolates identification. Report issues to Microbiology Supervisor.
- Use reference materials to source information to confirm identification results.
- Ensure adequate supplies of consumables and equipment.
- B - Validation & verification:

- Verification the performance of validation studies (IQ/OQ/PQ protocols and reports).
- Plan and co-ordination of activities related to validation studies.
- Carry out testing and interpretation and recording of results as per current validation protocols.
- Timely calibration and maintenance of laboratory equipment.
- Purchase of laboratory equipment and supplies.
- Prompt and timely investigation of any irregularities concerning validation testing or equipment calibration.
- Proper completion and review of logbooks associated.
- C- Analysis:

- Perform routine and non-routine microbiological analysis for finished product, raw materials, waters, and client samples according to the relevant testing procedures and report any problems or queries to the Microbiology supervisor.
- Perform environmental monitoring and non-routine monitoring as requested. Report any potential contamination sources to the Microbiology Supervisor. Interpret report and record these results in the appropriate continuous records.
- To assist in the preparation of laboratory materials to ensure that the laboratory is adequately provisioned.
- D- Administration:

- Assist in the preparation and updating of SOPs and other controlled documentation used within the Microbiology Department.
- Ensure all results are accurately and appropriately recorded in the correct location.
- Aid and assist other staff members as required.
- E- Compliance:

- Ensure that the Microbiology laboratory complies with the various regulations governing the pharmaceutical industry and laboratories by maintaining the laboratory in an auditable condition at all times.
- Ensure appropriate standards of cleanliness, tidiness and organization of the work environment is maintained.
- Report and investigate variances in test results.
- F- Microbiological Support:

- Participate in special project work in which the Microbiology Department is involved.
- Assist in the successful completion of the activities outlined in the Business Plan of the Microbiology Department.
- Communicate and provide support to personnel in other departments, in relation to microbiological issues.
- Communicate to and provide support & guidance to team members and assist them in the completion of tasks.
- The collation of all results and trending data, which is used to provide reports as deemed necessary by the Microbiology supervisor.
- Maintain current qualification status in testing procedures.
- G-Training:

- Undertaking training and reading of Standard Operating Procedures as required.
- Assist in Microbiology Training Modules for Cleanroom.
- Assist with the training of new team members in key team related tasks.
- H-Environmental Health and Safety:

- Participate in and take responsibility for workplace environment, health and safety at the level required for this position, following the guidelines in the company Environmental, Health and Safety Management System Manual.
- I- Data Integrity:

- 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.
- J- Other:

- Delegate for Microbiology Section head in case of his absence (if needed).
- Delegate Microbiologist in case of absence.
- The minimum qualifications for this role are:

- Bachel

We are looking for a Quality Control engineer to develop and execute exploratory and automated tests to ensure product quality.

Quality Control responsibilities include designing and implementing tests, debugging and defining corrective actions. You will also review system requirements and track quality assurance metrics (e.g. defect densities and open defect counts.)
Ultimately, you should monitor all stages of software development to identify and resolve system malfunctions to meet quality standards.

**Responsibilities**
- Review requirements, specifications and technical design documents to provide timely and meaningful feedback
- Create detailed, comprehensive and well-structured test plans and test cases
- Estimate, prioritize, plan and coordinate testing activities
- Design, develop and execute automation scripts using open source tools
- Identify, record, document thoroughly and track bugs
- Perform thorough regression testing when bugs are resolved
- Liaise with internal teams (e.g. developers and product managers) to identify system requirements
- Monitor debugging process results
- Investigate the causes of non-conforming software and train users to implement solutions
- Track quality assurance metrics, like defect densities and open defect counts
- Stay up-to-date with new testing tools and test strategies

**Requirements and skills**
- Proven work experience in software development
- 1- 2 Years Of work experience in software quality assurance
- Strong knowledge of software QA methodologies, tools and processes
- Experience in writing clear, concise and comprehensive test plans and test cases
- Hands-on experience with both white box and black box testing
- Hands-on experience with automated testing tools
- Solid knowledge of SQL and scripting
- Experience working in an Agile/Scrum development process
- Experience with performance and/or security testing is a plus

Ability to commute/relocate:

- Maadi: Reliably commute or planning to relocate before starting work (required)

Application Question(s):

- Are You a Computer Science Major ?

**Education**:

- Bachelor's (required)

**Language**:

- English (required)

_**Deciding what to do in the future is tough. We can HELP!**_

**MultiCare’s Internship Vacancies**

**Gaining a practical experience while studying is not easy!**

**Recognizing where you want to be post-graduate is not easy!**

**Being engaged and involved in day-to-day real business is not easy!**

**Having hands-on with professional mentors is not easy!**

As a commitment, at **MultiCare** Egypt for Pharmaceutical Industries we are not only aiming to enable Egyptians to live healthier but also as part of Corporate Social Responsibility we help undergraduates to develop a thorough understanding of where they want to take their career during their scholar.

This can be achieved through the placements and internship we offer where you will be engaged to most of Pharmaceutical Functions and Departments accordingly you develop tentative career compass to lead your future.

**A. What is in it for you?**
- **Living the Experience**

MultiCare Egypt for Pharmaceutical Industries offers intern opportunities across most divisions to undergraduates from a variety of academic backgrounds. The program offers a unique opportunity to utilize, enhance and develop skills particular to your studies in a practical and engaging environment.

Our internship program offers you the chance to have real responsibility so you can make an impact on the business, as well as offering dedicated support and development opportunities to help you get the most from your time with us.
- **Learning, Development and Career Counselling**

This Summer Internship Program suits students who want a career with a real purpose. A development program equips students with the knowledge, skills and attributes that are needed to identify where they best fit in the industry. Participants benefit from a rich variety of structured training, individual mentoring, and opportunities to experience different aspects of the business.

At the same time, MultiCare also seeks to build our talent pipeline with the best and brightest undergraduate students. A positive internship program experience can pave the way to a successful tomorrow, as you enjoy valuable networking opportunities and hands-on exposure to real time projects in key functional areas

Program Structure

**The duration of the placement is 8 - 10 weeks at the Quality Control specifically in the Chemical Lab**

**B. Requirement/Profile**:

- Fresh graduates Life-Science (Pharmacy, Medicine, Vet. and Science)
- Good linguistic skills bilingual English/Arabic
- Excellent interpersonal and communication skills
- Ability to work as a member of team and on own

**You can visit us via**:
**About the Company**:
**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 +22 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).

**Job Type**: Internship
Contract length: 2 months

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 +40 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 at New Cairo as well close by the facility. 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**:
For the Quality Control Function, we are hiring a **QC Finished Products Supervisor** per the following details:

- **Location **:New Cairo, Industrial Zone, Third Settlement
- **Reporting**:Quality Control Manager
- **Grade**:qC01/qC03

**Purpose**:
Successful incumbent will be responsible for conducting different types of tests and analysis further to finish products in a timely manner for in-process and finished products to ensure products specifications fulfil the prevailing standards governed by Regulatory and GMP practice.

**A.Essential Duties and Responsibilities**:
*
- Analyze finished products assuring strict compliance with standards prior to the release and report results with conformity statement
- Perform physical testing and chemical analysis of different pharmaceutical dosage forms including Tablets and Capsules
- Adhere to the approved controlled standard operating procedures and work instructions of finished product specifications and test methods whilst testing performing
- Test system modifications in order to get ready for new process implementations and introduce databases of known test deficiencies
- Maintain the quality control approved control records related to the daily work and adhere to the governing record-retention and archiving policy
- Calibrate instruments according to work instructions to ensure compliance to standards
- Fully abide by the instructions of Environmental, Health and Safety in handling all job related tasks and activities
- Perform wet and instrumental analysis (HPLC, UV Spectrophotometer, Viscometer, Titro-processor, pH meter, Balance, ovens, Centrifuge, Dissolution tester, Disintegration tester, Hardness tester, Friability tester)of bulk, in-process and finished products

*
- Work in a testing environment, assess products, check quality and accuracy, and create tests scripts
- Report and participate in investigation of any NCR with assigned cross functional committee as appropriate
- Create and/or review the Certificate of Analysis (Test Notes) presented to the MoH

**B. Job Requirements**:

- 3-5 Years post-graduate pharmaceutical manufacturing experience preferably in Quality Control Dept.
- Experience of same role at reputable Pharmaceutical companies
- Ability to work autonomically or a member of diversified cross
- functional teams
- Ability to prioritize activities, to make difficult decisions to ensure efficient use of resources and address critical issues impacting the business

**C. Knowledge**:
Pharmaceutical manufacturing understanding preferably at different functional areas like Production, QC, QA, etc among them most work experience desired at Quality Control Supervisory role

**D. Education Requirements**:
A degree in Pharmacy is ESSENTIAL. Related post-graduate qualification is highly desired (GMP, TQM, etc)

**E.Competencies and Behaviors**:

- Indisputable leadership capabilities
- Strategic thinking and planning skills
- Excellent written and verbal skills in English
- Ability to handle simultaneously parallel task with quality delivery

**What we offer**:
With us, there are always opportunities to break new ground. We empower you to fulfill your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!

Ability to commute/relocate:

- Cairo: Reliably commute or planning to relocate before starting work (preferred)

Build a new team for the challenges of the new busbar

Methode Electronics is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, genetic information and other legally protected characteristics per the EEO