96 Scientific Research & Development jobs in Egypt

Company Description

Groovy Aesthetic Clinics focus on holistic wellness, providing state-of-the-art, medical-grade spa services. Located in Heliopolis, our range of products and services includes skin-care treatments like derma fillers, laser procedures, nutritional services, spa treatments, and a complete, modern gym. Distinguishing Groovy from other spas is our high standard of professionalism and medical care, comparable to that of any medical clinic or hospital. All services are supervised by experienced doctors and medical professionals to ensure safe and effective procedures, all in a relaxing and comfortable atmosphere.

Role Description

This is a full-time, on-site role for a Quality Assurance Specialist (Pharmacist) at Groovy Aesthetic Clinics in Heliopolis. The Quality Assurance Specialist will be responsible for overseeing and maintaining the quality of our spa's medical services. Day-to-day tasks include quality control, quality assurance, implementing quality management systems, and ensuring adherence to Good Manufacturing Practice (GMP). The Specialist will also conduct quality audits to ensure compliance with regulatory standards.

Qualifications

• Skills in Quality Control, Quality Assurance, and Quality Management
• Knowledge and application of Good Manufacturing Practice (GMP)
• Experience in Quality Auditing
• Excellent attention to detail and analytical skills
• Strong organizational and communication skills
• Ability to work in a team-oriented environment
• Bachelor's degree in Pharmacy or related field
• Experience in the healthcare or cosmetics industry is a plus

Job Title:
Senior Research and Development Engineer

Job Description:

We are seeking a highly skilled Senior R&D Engineer
to join our team. The ideal candidate will be responsible for leading innovation, driving new product development, and improving existing products to meet market demands and organizational goals.

Key Responsibilities:

• Lead and manage R&D projects from concept through to production.
• Conduct research, feasibility studies, and develop prototypes.
• Design, test, and validate new products and processes.
• Collaborate with cross-functional teams (design, manufacturing, quality, and supply chain).
• Provide technical expertise and mentor junior engineers.
• Monitor industry trends and integrate new technologies into product development.
• Ensure compliance with safety standards, regulations, and quality requirements.

Qualifications:

• Bachelor's or Master's degree in Engineering (Mechanical, Electrical, or related field).
• Proven experience (5+ years) in R&D or product development.
• Strong knowledge of CAD tools, prototyping, and testing methods.
• Excellent problem-solving and analytical skills.
• Strong communication and leadership abilities.

Company Description

MICO WORLD is an Internet company specializing in the social entertainment industry. It has developed several popular social entertainment applications, including MICO, YoHo, TopTop, and SUGO. With a strong presence in markets like the Middle East, Southeast Asia, North America, Japan, and Korea, MICO WORLD operates in over 150 countries and regions. The company boasts over 200 million global registered users of its products.

Role Description

This is a full-time on-site role for a Quality Assurance Specialist - Live streaming, located in Cairo, Egypt. The Quality Assurance Specialist will be responsible for conducting quality control and assurance tasks, ensuring compliance with quality standards, and implementing quality management practices. Day-to-day tasks will include monitoring live streaming content, performing quality audits, and ensuring adherence to Good Manufacturing Practice (GMP).

Qualifications

• Quality Control, Quality Assurance, and Quality Management skills
• Quality Auditing skills
• Excellent attention to detail and problem-solving skills
• Strong communication and teamwork abilities
• Relevant experience in the live streaming or social entertainment industry is a plus
• Fluency in English

About Minapharm:

Minapharm Pharmaceuticals is a leading pharmaceutical company in Egypt and the Middle East and the largest end-to-end manufacturer of biological therapies in MEA with over 20 years of experience in cellular and bioprocess engineering. Headquartered in Cairo, Minapharm commercializes over 100 lifesaving and life-enhancing products ranging from small molecules to complex bioengineered proteins and viral vectors, with an impressive immunotherapy pipeline. Together with its wholly owned Berlin-based subsidiary, ProBioGen AG - a world-leading CDMO, Minapharm has established an integrated business model making it the only gene-to-market company in the region. Consolidating its international platform of intelligent biopharmaceutical technologies with the longstanding process development and manufacturing expertise in the MEA, Minapharm, together with ProBioGen, has incorporated MiGenTra GmbH headquartered in Berlin and manufacturing in Cairo, to enhance the accessibility to critical healthcare transforming medicines through product development and commercialization of Biosimilar mABs, Cell, and Gene Therapies and vaccines, at affordable prices in Egypt, and MEA.

Our Values:

• Diversity & Respect
• Integrity & Accountability
• Collaboration
• Leadership & Empowerment
• Innovation & Continuous Learning

QA Compliance Specialist Job Summary:

Perform all quality assurance compliance activities including but not limited to GMP and pharmaceutical quality system compliance, gap analysis, internal audits, supplier audits, PQR, complaints, quality risk management and GMP training.

QA Validation Specialist Job Summary:

To execute qualification and validation for all manufacturing and cleaning procedures.

QA Compliance Specialist Duties & Responsibilities:

1. Participate in update procedures relevant to pharmaceutical quality system compliance, gap analysis, internal audits, supplier audits, quality risk management and GMP training.
2. Participate in annual internal audit schedule, prepare internal audit reports, send approved internal audit reports to owners, agree with owners on SMART CAPAs, follow up closure of CAPA and evaluate CAPA effectiveness and quarterly report status of internal audit QKPIs.
3. Participate in audits of supplier / contractor / contract acceptors, prepare audit reports, send approved audit reports to supplier / contractor / contract acceptors, agree with them on SMART CAPAs, follow up closure of CAPA and evaluate CAPA effectiveness and quarterly report status of supplier / contractor / contract acceptors audit QKPIs.
4. Ensure that all employees (permanent, temporary) and contractor / visitors receive required GMP training before they independently certified to perform their tasks independently.
5. Prepares a register of qualified trainers, participate in preparation of training programs, participate in evaluation of training effectiveness and quarterly report status of GMP training QKPIs.
6. Participate in all quality risk management activities with cross-functional teams of SMEs. Follow-up closure of all actions required to reduce risks to an acceptable level and evaluate effectiveness of these actions through after-action risk review. Quarterly report status of quality risk management QKPIs.
7. Work with cross-functional team to develop and maintain site contamination control strategy. Prepare a quarter report indicating status of contamination control strategy and its effectiveness in controlling contamination and cross-contamination risks and recommendations for improvement.
8. Perform PQR data collection, review, analysis and reporting for all manufactured products. Set recommended actions and required SMART CAPA with follow up closure of CAPA and evaluate CAPA effectiveness and quarterly report status of PQR reports in QKPIs.
9. Handling of received Customer Complaints ( starting from receiving of complaint, numbering, evaluation and investigation, impact assessment, set SMART CAPA, immediate action and CAPA follow up, closure and trending )
10. Participate in different multidisciplinary teams and relevant activities as required.

QA Validation Specialist Job Responsibilities:

1. Follow equipment calibration plan and coordinate with concerned departments to perform qualification/validation activities.

2. Witness equipment qualification/calibration activities and review qualification documents and calibration certificates supplied by external service providers.

3. Prepare protocols, execute qualification protocols and report outcomes for process and cleaning validation in addition to Equipment / Utilities qualification.

4. Issue new SOPs and revise SOPs as requested.

5. Record incidents, deviations, changes and participate in the investigation and assessment.

6. Implementation of CAPA, additional controls, change control actions, annual report actions, management review actions.

7. Execute quality risk management-projects, health and safety risk-assessment and environmental aspects & impacts.

8. Perform on-site training sessions as relevant.

Needed qualifications:

• 1-3 years in pharmaceutical industry preferably experience in quality operations & in sterile manufacturing, hands on experience in validation activities.
• Minimum BSc in pharmaceutical sciences is a must.
• GMDP requirements for sterile biological products.
• Ability to implement and follow-up of validation or qualification requirements.
• Ability to evaluate data generated from validation studies.
• Basic GMP.
• Proficiency in English language.

Job Location:
10th of Ramadan.

• Transportation is provided.
• Medical Insurance.
• Life Insurance.
• Profit share.

Good Luck to All

Responsibilities:

• Develop procedures to ensure that Quality System documents are originated, changed, reviewed, distributed, archived and periodically reviewed using systems that are efficient and meet all regulatory requirements.
• Develop and maintains systems that effectively archive and retrieve quality records assigned to the Document Control, including external standards, technical reports, etc.
• Ensure that the Document Control systems used at all company sites are harmonized where appropriate.
• Prepare periodic summaries of document and record control activities, including the analysis of the types of changed documents, change order cycle times.
• Follow-up filling & packaging inkjet data, analysis results and release batches on Oracle system for Exportation invoices.
• Follow up the exportation registration requirements (samples, certificates, specifications, methods of analysis and letters) for the exportation department.
• Organize and coordinate with the external audit authorization to proceed and follow surveillance and recertification audits.
• Determine weighing of Toll Manufacturing products for filling process.
• Creation, update & issue batch records required for production – Filling & Packaging.
• Creation, update & issue batch records required for production – Mixing & filling and packaging – for toll manufacturing products.
• Follow up toll manufacturing requirements and documents.

Qualifications

Education:
Bachelor Degree in any relevant discipline.

Years of experience:
3-5 years of experience.

Computer skills: Very
good Computer skills proficiency (Microsoft Office and Oracle).

Language skills:
Very good English Language.

What will you do:

• Drive new product development across the Easy Care category.
• Lead laboratory testing, pilot runs, and validation of raw materials and finished goods.
• Optimize formulations, improve product performance, and enhance efficiency.
• Introducing new technologies, materials, and continuous improvement initiatives.
• Collaborate with Operations, Marketing, Quality, Supply Chain, and Regulatory teams.
• Ensure full compliance with national and international regulations.
• Lead, mentor, and inspire the R&D team.

What you will need:

• Bachelor's or Master's in Chemical Engineering, Chemistry, or related Science field.
• 10+ years of R&D experience, preferably in FMCG or hygienic products.
• Strong knowledge of raw materials, formulations, and production technologies.
• Proven success in taking products from concept to commercialization.
• Familiarity with ISO, GMP, and sustainability practices.
• Strong leadership, project management, and problem-solving skills.

You'll love this job if you're:

• Passionate about innovation and eager to bring ideas to life.
• Excited by the challenge of turning concepts into products that impact millions.
• A natural leader who thrives on mentoring and developing teams.
• Detail-oriented but always keeping the big picture in mind.
• Motivated by solving problems and driving continuous improvement.
• Someone who values collaboration across functions and cultures.

Company Description

Pharco Corporation, a leading pharmaceutical group, is dedicated to the development, manufacturing, marketing, distributing, and exporting of branded and generic drugs. With operations dating back to 1987, Pharco has grown to employ 5700 individuals and ranks number one in the Egyptian pharmaceutical market. The company's mission is to provide highly effective and safe pharmaceutical products at affordable prices.

Role Description

• To Develop & Update R&D Methodology activities related to (Testing methods of new & current products to ensure effective Analytical & Cleaning testing Methods supports Process & Product conformity throughout Product life cycle.
• Analyze research and development samples.
• Develop new analysis methods for products.
• Update analysis methods.
• Ensure the accuracy of the analysis methods.
• Conduct comparative studies to compare the company's product with the global reference product.
• Comply with the company's policies and regulations.

Qualifications

• Bachelor's degree in pharmacy or science
• 1 to 3 years' experience in Pharmaceutical Industry (a similar role)
• Exposure and hands-on different roles at different manufacturing disciplines (e.g. Production, Quality, Engineering, EHS)
• Very Good verbal, written and interpersonal communication skills. English fluency is essential

Main Tasks:

• Conduct audits across all departments, including Customer Service, Sales, Customer Experience, Operations, and Back Office.
• Ensure compliance with company policies, industry regulations, and quality benchmarks.
• Identify process gaps, inefficiencies, and risks, recommending corrective actions and improvements.
• Monitor the implementation of quality assurance measures and maintain accurate documentation of audit findings.
• Provide data analysis and performance reports to senior management, highlighting trends and areas for improvement.
• Develop strategies to enhance operational efficiency, service quality, and compliance.
• Deliver training sessions, refresher courses, and coaching to employees on quality standards, audit procedures, and best practices.
• Mentor and support teams to ensure adherence to operational protocols.
• Customer Service & Quality Monitoring:
• Conduct quality assessments of customer interactions (calls, emails, and chats) to ensure service excellence.
• Implement quality assurance procedures to enhance customer experience and satisfaction.
• Work closely with teams to address quality-related issues and customer concerns.
• Collaborate with department heads to optimize processes and streamline operations.
• Stay updated on industry trends, regulatory changes, and best practices to drive continuous improvement.

Requirements:

• Bachelor's degree in a relevant field.
• From 1 to 3 years of experience in quality assurance, auditing, or process improvement.
• Strong analytical, problem-solving, and reporting skills.
• Excellent communication and interpersonal abilities.
• Familiarity with quality standards, compliance regulations, and operational audits.
• Holds a Quality Certification or has completed a relevant course (e.g., Lean Six Sigma, TQM, or ISO 9001 Auditor Certification) is preferred.

Interested candidates please send your CV to with Quality Assurance Specialist in the subject.

Job Type: Full-time

Application Question(s):

• What is your current and expected salary?

Experience:

• Quality Assurance: 1 year (Preferred)

The information extraction team in shopping is seeking a highly motivated and talented Applied Scientist to work on cutting-edge technologies in the field of information extraction in the shopping domain.

As an Applied Scientist you will gain extensive experience in information extraction using the latest AI advances and LLMs. You will gain valuable experience in building real-world information extraction systems at a Web scale. This opportunity will allow you to use cutting-edge AI technologies, accelerate your career growth and develop deep business acumen.

Microsoft's mission is to empower every person and every organization on the planet to achieve more. As employees we come together with a growth mindset, innovate to empower others, and collaborate to realize our shared goals. Each day we build on our values of respect, integrity, and accountability to create a culture of inclusion where everyone can thrive at work and beyond.

• You will gain a basic understanding of a broad area of research and applicable research techniques. You'll also develop a basic knowledge of industry trends and share your knowledge with immediate team members.
• You will apply strategies provided by senior team members. Following guidance from team leaders, you'll also research relevant tools and technologies being used in the community.
• You will reinforce a positive environment by learning and adopting best practices. Additionally, you will also maintain or develop ties with an external network of peers and identify prospective talent for Microsoft research pipelines when asked.
• You will assist with documentation for senior team members, as needed.
• You will also learn and follow ethics and privacy policies while executing research processes or collecting information.

Required Qualifcations:

• Bachelor's Degree in Computer Science, Electrical or Computer Engineering or related field AND relevant internship experience (e.g., statistics, predictive analytics, research)
• OR Master's Degree in Computer Science, Electrical or Computer Engineering, or related field
• OR equivalent experience.
• You must be legally authorised to work in Egypt to be eligible for this role (Legally authorised = has citizenship or has been granted a valid visa or work permit)
• Fluency in English

Preferred Qualifications:

• Bachelor's Degree in Computer Science, Electrical or Computer Engineering,
• OR related field AND 2+ years related experience (e.g., statistics, predictive analytics, research)
• OR Master's Degree in Computer Science, Electrical or Computer Engineering, or related field
• OR equivalent experience.
• Solid machine learning/AI/LLM knowledge.
• Experience building and deploying ML/Ai systems including investigation, prototyping, deployment and continuous measurement.
• Solid knowledge of python/other ML languages and frameworks.

Microsoft is an equal opportunity employer. Consistent with applicable law, all qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, color, family or medical care leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran or military status, race, ethnicity, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable local laws, regulations and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application process, read more about requesting accommodations.