Deputy QPPV

Apex Multi-Apex Pharma is hiring a Deputy QPPV
Job requirements:
• Pharmacy graduate
• Completed PV training courses required by EPVC.
• At least one year Experience as a deputy QPPV.
• Experience in preparing PSUR, RMP, ICSR reporting…etc
• Excellent command of both written and spoken English.
• Presentable.
• Having a valid driving license. Kindly send your updated resume with a recent photo within one week.
E-mail subject: Deputy QPPV to


Habib Scientific office
+ We are announcing vacancies for (full time medical representative)
+ Area : Only in helwan district.
+ only vet or pharmacy graduates.
+ fresh graduated or experienced candidates.
+ Offer : A very attractive package and incentive scheme + Medical insurance Life insurance + Mobile line + USB modem
+ To apply send your CV to :
+ For more info call :
01224320306 ( dr mina )

+ لخريجي طب بيطري وصيدلة فقط
+ المرشحين من حديثي التخرج او اصحاب خبرة
+ يمكنك ارسال ال CV علي الايميل التالي :
+ لمعرفة التفاصيل يمكنك الاتصال :
01224320306 ( د/ مينا )


SEDICO pharmaceutical Co. plant in 6th of October city is hiring PRODUCTION PHARMACIST with the following qualifications

 Faculty of pharmacy graduate. (male only)

From 3 to 5 years experience

 Preferred Giza or October residency.

Completed or exempted military service If you meet the previous criteria

send your updated CV to and mention the job title in subject area

صيدلي/مساعد صيدلي/مبيعات/مدير مشتريات ادوية

Job Sender

مساعد صيدلي 
متخصص مبيعات تجميل
مدير مشتريات ادوية
الخبرة:لا تقل عن سنتين
مطلوب أيضا طيارين
لمجموعة صيدليات في الهرم 
برجاء إرسال السير الذاتية
والتواصل مع الرقم الاتي

Regulatory Affairs Specialist

Job Title Regulatory Affairs Specialist
Vacancy Deadline(mm/dd/yy) 3/31/2017

Languages English
Languages English, Excellent
Country Egypt
City Giza
Job Category Pharmacy
Job Type Full Time
Job Level Senior

-Prepare the regulatory documents needed to attain the approval of regulatory agencies needed for the registration of pharmaceutical products in addition to acting as the liaison between HIKMA and the regulatory authorities.
-Preparing clear arguments, explanations and presentations for regulatory organizations to resolve any issues related to new product licenses, renewals and variations.
-Reviewing company related practices, handling regulatory inspections and providing advice on required modifications to Hikma systems according to governmental policies and regulations.
-Writing clear comprehensive product labels and leaflets in compliance with regulations and specifications.
-Performing other duties related to the job as assigned by the direct supervisor.

Bsc. of Pharmacy
Gender Any
Car owner Any
Education major English
Experience 3 – 5 Years.

Other Skills
1.Concern for Quality
2.Follow-up & Coordination
3.Work Ethics & Values

Excellent remuneration package, Medical Insurance, Profits, incentive, life insurance, Annual Bonus, etc.
Salary (L.E.) Negotiable

Comments Kindly Send Your CV with A RECENT PHOTO, Stating job title in the subject .

Job Contact Email

QC Analyst

Employer Rameda Pharmaceuticals
Job Title QC Analyst

Vacancy Deadline(mm/dd/yy) 4/30/2017
Languages English, Excellent
Country Egypt
City Giza
Job Category Pharmacy, Chemistry, Quality Control
Job Type Full Time
Job Level Junior

1. To analyze all Raw Materials (initial and retest), vendor lots, and Non HPLC Finished Products (validation) according to company procedures and using some reference books (USP, EP, BP, etc.)
2. To analyze Qualification and Registration samples of new products
3. To test the Cleaning Validation samples
4. To perform Non HPLC Bulk Validation testing.
5. To analyze the purified water and water for Injection of Lactam and N/L water system.
6. To prepare and standardize of Volumetric Solutions, Reagents, Standards and Mobile Phases.
7. To perform the LIMS Activity on Computer as follows – Update loading data to get the results of the tested item. – Print out all work sheets for the tested items and their COAs. 8. To Perform the chemical testing for validation of sterile areas equipments
9. To perform testing according to company policies and GMP/GLP roles.
10. Calculation of results and issuing COA. In case of any abnormal results will inform direct supervisor.
11. Evaluation of results and reports affect releasing the Raw Material to production.
12. Any other duties and responsibilities as may be required from time to time by Section Head.
13. Ensures that all activities in his unit or section are done according the relevant cGMP and ISO standards (ISO 9001/2008, ISO 14001/2004, and OHSAS 18001/2007).

BSc of science or pharmacy, experience of 1 to 3 experience, Very good in English, Computer skills, flexibility, effective communication skills, Ability to solve problems,

Preferable October or Sheikh zaiyed resident.
Gender Any
Car owner Any
Education major Pharmacy
Experience 1 – 2 Years.

Other Skills Good Communication skills, Analytical character, result oriented, self-motivated.
Salary (L.E.) Negotiable

Job Contact Email Please send your CV to the following mail address quoting job title ,