83 Pharmaceutical jobs in Egypt

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.

Job Summary

We are seeking a passionate and talented Pharmacovigilance Specialist to join our dynamic team.

The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry.

Key Responsibilities:

• Ensuring the necessary quality, including the correctness and completeness, of pharmacovigilance data submitted to EDA.
• Ensuring a full and prompt response to any request from EDA for the provision of additional information necessary for the benefit-risk evaluation of a pharmaceutical product.
• Providing any other information relevant to the benefit-risk evaluation to EDA.

Requirements

• Bachelor's degree in pharmacy, or Medicine.
• 1-2years of pharmaceutical experience.
• Certification in pharmacovigilance (e.g., Certified Pharmacovigilance Professional - CPVP) is a must

Job Title:
Medical Representative (Zayed Area)

Location:
Sheikh Zayed, October Area – Egypt

Industry:
Pharmaceuticals / Nutrition

Specialty:
Peptides & Nutrition

Job Type:
Full-Time

Job Overview
We are seeking a highly motivated and well-connected
Medical Representative
to join our team, specializing in
peptide-based products
. The ideal candidate must have
strong relationships with nutrition doctors
in the
October and Sheikh Zayed
areas and be familiar with the territory.

Key Responsibilities

• Promote and detail peptide-based pharmaceutical products to healthcare professionals, especially nutritionists and dietitians.
• Build and maintain strong, long-term relationships with doctors in the assigned territory.
• Execute sales strategies and achieve targets for the assigned area.
• Provide accurate product knowledge and handle objections professionally.
• Regularly report on field activities, market feedback, and competitor insights.
• Participate in conferences, meetings, and training sessions as required.

Requirements

• Bachelor's Degree in Pharmacy (mandatory)
• Proven experience as a Medical Rep, preferably in nutrition or peptide-related products
• Strong network and existing relationships with nutrition doctors in October/Zayed
• Deep knowledge of the Zayed/October area and its healthcare landscape
• Excellent communication, negotiation, and presentation skills
• Self-motivated and target-driven

What We Offer

• Competitive salary and commission structure
• Continuous training and professional development
• Supportive team environment
• Opportunities for growth within a dynamic and innovative company

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at

Job Function
Regulatory Affairs Group

Job Sub Function
Regulatory Product Submissions and Registration

Job Category
Professional

All Job Posting Locations:
Cairo, Egypt

Job Description
Summary of the job:
The main task of a Regulatory Affairs Specialist in Johnson & Johnson is to Develops skill set to enable value added individual contributions, who works under close supervision. Applies methods for planning, directing, coordinating and controlling regulatory affairs activities related to new and modified products worldwide in compliance with corporate policies and strategies. Interprets new and changing government regulations to ensure compliance with regulatory/ government standards.

Duties & Responsibilities
Assists by providing knowledge in implementing compliance with regulations to enable products that are developed, manufactured, or distributed meet regulatory agency requirements.

Applies functional analysis and interpretation of scientific data in assessing risk and creating regulatory strategies to expedite new product introductions to the market.

Contributes on cross-functional project teams in the development of compliant policies and operational plans to ensure timely commercialization of new and modified products into key markets.

Advises product development teams on input for product labeling, claims support, promotional and scientific materials, and other related activities to ensure all regulatory requirements are met throughout the development process.

Carries out the detailed regulatory submissions required for new and existing product approvals and registrations.

Coordinates Regulatory Affairs interpretation and feedback in support of federal, state, and/or international regulations by preparing documentation and reports to support internal and external audits.

Understands and applies Johnson & Johnson's Credo and Leadership Imperatives in day-to-day interactions with team.

This job is salaried.

• Education: a bachelor's degree in a life-sciences-related field like pharmacy, Science, or Veterinary Medicine
• Experience: 3-4 Years of experience in Regulator affairs working in multinational Medical Devices company
• Having an experience in dealing with Healthcare Authorities
• Language: Arabic, English, French (all are must)
• Location: Cairo, Egypt
• Relocation availability: No

Job Responsibilities:

• Develop and execute marketing plans and strategies.
• Conduct market research and competitive analysis to
• Identify new opportunities.
• Manage the launch and promotion of new products. .
• Collaborate with the sales team to provide training, support, and marketing tools.
• Monitor product performance and market trends, adjusting strategies as needed.
• Work closely with medical and regulatory teams to ensure compliance with industry standards.
• Build strong relationships with key opinion leaders (KOLs) and healthcare professionals.
• Manage budgeting and forecasting for assigned products.

Requirements:

• Minimum 1-2 years of experience as a Product Manager.
• Good relationships with GIT and IM doctors
• Good relationships with Gynecologist , maternity hospitals and IVF doctors
• Proven success in new product launches is a plus.
• Bachelor's degree in Pharmacy, Veterinary Medicine, or Science.
• Holding an MBA or Marketing Diploma is an advantage.
• Strong analytical and strategic thinking skills.
• Highly energetic, proactive, and results-driven.

Apply Now

Send your CV on with the subject line:
Product Manager- your specialty

Join Splendid Pharma and be part of a growing, innovative, and people-centric pharmaceutical company.

Splendid Pharma is looking for passionate and ambitious Medical Representatives to join our team, If you are a results-driven professional with a strong medical background and a desire to grow in the pharmaceutical industry, we want to hear from you

Requirements:

• Bachelor's degree in Pharmacy, Medicine, Veterinary, or Science (Biology/Chemistry-related fields)
• 0-3 years of experience in medical sales (Fresh graduates are welcome)
• Strong communication, negotiation, and presentation skills
• Self-motivated, ambitious, and target-oriented
• Ability to work independently and as part of a team
• A valid driver's license is preferred

What We Offer:

• Competitive Salary 15K+
• Attractive Incentive Scheme
• Medical and social insurance
• Career Growth Opportunities
• Continuous Training & Development
• A Dynamic & Supportive Work Environment

Apply Now

send your CV on with your title and area on the subject

Join Splendid Pharma and be part of a growing, innovative, and people-centric pharmaceutical company.

Job Title:
Junior Italian Quality Assurance Analyst.

Location:
Work from home.

Working Hours:
09:00 - 18:00 Portugal Time.

Work Week:
Monday to Friday.

Department:
Digital Services and Transformation; Operations.

Reports To:
Operations.

Position Overview:

The Quality Assurance Analyst is responsible for evaluating transactions between Operations Customer Experts (OCEs) and Customers (Voice, Email, Chat, Click-to-Call, social media or other channels) to identify and suggest opportunities for improvement within the project's processes in order to help TP meet our client's expectations and increase our end user's, OCEs and client's satisfaction.

Key Responsibilities

(may perform other duties as requested, not specifically addressed in this document)

Maintain independence and objectivity while evaluating and assessing OCEs quality performance. Ensuring independence in Quality Assurance (QA) evaluations of Operations Customer Experts (OCEs) is crucial to maintaining fairness, accuracy, and credibility. Independence means that QA analysts evaluate OCE performance objectively, free from personal biases or external influences, by adhering to the following principles:

• Avoid Conflicts of Interest: QA analysts should not evaluate Operations Customer Experts they supervise or work closely with to prevent biased assessments.
• Objective Oversight: Ensure QA analysts do not have personal or professional relationships with the Operations Customer Experts being evaluated. If this is the case, the evaluations must be performed by another Quality Assurance Analyst.
• Calibration Sessions: Regularly conduct calibration meetings to align evaluators and ensure consistent interpretation and application of evaluation criteria.
• Detailed Evaluations: QA analysts must clearly document the rationale for each score, providing specific evidence from the call or interaction to support their assessments.
• Spot Checks on Supervisor Evaluations: Conduct periodic spot checks on evaluations performed by Operations Supervisors to verify accuracy, consistency, and adherence to established QA guidelines. This helps identify and correct potential biases or discrepancies in their assessments.
• Findings/identification that allow the improvement of OCEs - Operations Customer Experts and operational results.
• Consistency.
• Identify risks in the projects and suggest ways of internal control to mitigate the associated risks.
• Identify potential fraud and security-related issues: short calls, authentication, tools, sales, referrals.
• Provide valuable information about the project to the Quality Assurance Assistance Manager.
• Deliver productivity.
• Identify training needs.
• Reporting of nonconforming situations; End Customers support through calls (inbound and outbound) and other channels (chat, email, click to call, back office.).
• Interaction with other departments in order to improve or maximize results.
• Be an active part in the processes of continuous improvement, proposing improvement and innovations methods across the department and the company (producing fresh and imaginative ideas and solutions).
• Ensure all TP processes, procedures and policies are fulfilled.

Required Qualifications:

• Education and specific Training: Bachelor's degree or Graduate (preferentially).
• Fluency in Italian and English.
• Work Experience: up to two years of experience in Contact Center.

Soft Skills &Other Requirements:

Technical Skills Hiring Requirements:

• Working knowledge of Microsoft Office Suite (Excel, Word, PowerPoint).
• Understands contact center business and trends.
• Analytical skills and proactive reporting insights. Skills to be trained:
• Client Product Training; Use of production tools.
• Use of phone - email System.
• Use of BMS System.

Competencies and specific skills:

• Achievement oriented.
• Communication skills.
• Customer oriented.
• Diversity orientation.
• Judgment.

لو حابب تنضم لكيان كبير و بيكبر كل يوم و هتكبر معاه

صيدلية وايت فرع حدائق الاهرام ترحب بالصيادلة

الشروط

(يفضل خبره لا تقل عن سنة في مجال الصيدليات)

1- مرتبات مميزة تفوق اسعار السوق

2- حوافز قيمة شهريا

3- اجازات سنوية مدفوعة الاجر

4- تأمينات حسب الرغبة

5- دورات تدريبية

سجل بياناتك و انت اشتغلت في مجال الصيدليات و حابب تنضم لينا او ابعت ال CV بتاعك علي

We're Hiring Regulatory Affairs and Logistics Specialist

Are you ready to start your career in the medical devices field?

Medica technology for health care product announcing for an expansion is looking for a Regulatory Affairs and logistics Specialist to join our growing team

Location: Mokattam

Employment Type: Full-Time

On-site
(8 AM to 4 PM)

2 Days Off

Requirements:

• Bachelor's degree in a science or Vet

• At least one year of experience in medical devices approvals and registration

• Proficiency in spoken & written English and Arabic

• Attention to details

• Excellent communication and negotiation skills

• Problem solving and time management skills

• Good attitude and willingness to learn

• Familiarity with government transactions is a plus

Job Description:

1- Prepare and submit all documents required for Importation approvals, customs release and customs exemptions.

2- Prepare registration file for our products.

3- Follow up on the registration process of each file and submit the vigilance year by year.

4- Communicate with the suppliers to confirm each order according to our plan.

5- Follow up with the shipping companies until the shipment arrives at our port.

6- Issuing the shipping documents of each shipment and issuing the ACID number.

7- Follow up with the customs companies until the shipment arrives at our warehouse.

If you're ready to take your first step in the medical industry and grow in a professional, supportive environment, we'd love to hear from you.

Benefits:

• Medical Insurance

• Social Insurance

• A Good Work Environment 

• A supportive environment for learning and growth.

If you're ready to take your
first step in the medical industry
and grow in a
professional, supportive environment
, we'd love to hear from you

To Apply:
Send your CV to

For inquiries:
WhatsApp

Are you a detail-obsessed professional with a passion for operational excellence and quality assurance? Jamjoom Pharma is seeking a dynamic Senior Validation Executive to drive precision, compliance, and efficiency in our fast-paced Quality team. This is your chance to make a measurable impact in one of the region's leading pharmaceutical companies.

Key Responsibilities:

• Ensure all validation activities comply fully with current Good Manufacturing Practices (cGMP).
• Prepare the Validation Master Plan and maintain the full validation lifecycle.
• Collaborate cross-functionally with Manufacturing, Quality Control, Engineering, and Regulatory Affairs.
• Support regulatory inspections and internal audits as a subject matter expert.
• Prepare and execute Aseptic Process Simulation (APS) protocols and reports.
• Develop and implement Cleaning Validation protocols aligned with global standards.
• Author and execute validation protocols (IQ/OQ/PQ) for equipment, APS, utilities, manufacturing processes, and cleaning procedures.
• Lead and manage smaller validation projects from initiation to completion.
• Analyze validation data, identify discrepancies, and author comprehensive summary reports.
• Investigate and resolve validation deviations and non-conformances.
• Collect, review, and verify complete documentation for validation processes.
• Prepare Process Validation files for export markets, including CTD and eCTD formats.
• Lead Performance Qualification (PQ) for machines, utilities, and production equipment.
• Prepare Computerized System Validation (CSV) protocols and reports to support data integrity and system compliance.
• Drive validation strategy in collaboration with QA, Production, Engineering, and RA teams.

What We're Looking For

• Proven experience in pharmaceutical validation.
• Strong knowledge of international regulatory frameworks (ICH, WHO, FDA, EMA, GMP).
• Detail-oriented, organized, and proactive leadership style.
• Excellent documentation, communication, and analytical skills.
• Strong problem-solving abilities and a collaborative team spirit.

Qualifications & Experience

• Bachelor's degree in Pharmacy.
• Minimum 8+ years of hands-on experience in Validation and Qualification within the pharmaceutical industry.
• Proven experience preparing CTD/eCTD dossiers for international markets.
• Hands-on execution of validation protocols including Equipment Qualification, CSV, Media Fill, Cleaning Validation, and Utilities Qualification.
• Deep understanding of cGMP, FDA 21 CFR Part 211, EU Annex 15, and other relevant guidelines.
• Ability to manage multiple priorities in a dynamic environment.