القائمة الرئيسية

الصفحات

 Minapharm Pharmaceutical Vacancies 


Minapharm Pharmaceutical Vacancies





1-Biotechnology Production Specialist 

Qualifications:


Bachelor’s degree in Pharmaceutical or Biotechnology Sciences or other related field.

Experience: 0-3 years

Excellent communication in English (oral and written).

Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.



What we offer:


Transportation

Meal

Life & Medical Insurance

Profit Share

Working hours from 8:00 AM till 4:30 PM

5 working days from Sunday to Thursday.


Apply Here




2-Semisolid Production Pharmacist  

Job description
Minapharm is one of the leading pharmaceutical and biopharmaceutical companies in Egypt, Africa, and the Middle East striving to provide innovative yet affordable treatments. Making a difference and supporting our community is our main priority aligned with our mission, so we are looking for hardworking, creative, and data-driven calibers with strong communication and leadership skills allowing them to integrate well and work with diverse teams in an effective and resourceful way.

Title: Semisolid Production Pharmacist - 2nd shift

Summary:

Responsible for all operations & procedures done in the Semisolid & liquid department during the second shift.

Duties:

Monitor drugs manufacturing in the semi-solid department according to cGMP.
Ensure that all production equipment are maintained in good working order.
Ensure the availability of all required materials.
Take corrective and preventive actions in case of deviations.
Check and revise the preparation, filling & packaging processes according to Batch record and relevant SOPs.
Perform any additional tasks as requested.

Requirements:

Education: Pharmacy Graduate is a must.
Experience: 0 – 3 years experience.
Work Location: 10th of Ramadan.
Working Hours: From 3:00 PM to 11:00 PM.
Good Command of English Language.
Good communication skills.
Transportation is provided.
5 working days.

Apply Here


3-Research Specialist - Protein Stability & Drug Product Development 

Job description
Main job duties/tasks:

Performance and execution of experiments which are related to the improvement, implementation and validation of analytical methods for stability testing of products including all necessary documentational aspects.
Participate in overall drug product development including pre-formulation studies, selection of excipients/formulation buffer studies and lyophilization development. This applies to all potential dosage forms (prefilled syringes/vials, lyophilized powder,..).
Participate in screening of primary packaging material for each development project and establishing container closure integrity including extractables & leachables studies.
Participate in design and compatibility testing of the final sterile filtration step and subsequent filling procedures.
On-time planning of stability programs according to ICH guidelines.
Supporting and cooperation with Protein Characterization department in terms of method development/improvement and troubleshooting if applicable.
Issuing relevant standard operation procedures (SOP’s).
Analysis and evaluation of results including troubleshooting.
Documentation and filing of results.
Project related literature screening.
Writing of regular reports.
Communication with other departments such as upstream, protein purification, protein characterization, ware house, purchasing, etc.
Correspondence with international partner companies.

Qualifications:

Bachelor’s or Master’s degree in Pharmaceutical or Biotechnology Sciences or other related field.
Previous experience in instrumental analysis (eg. HPLC) is preferable up to 2 years.
Strong computer, scientific, and organizational skills.
Excellent communication in English (oral and written).
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.

Location: 10th of Ramadan, Sharkia, Egypt

What we offer:

Transportation
Meal
Life & Medical Insurance
Profit Share
Working hours from 8:00 AM till 4:30 PM
5 working days from Sunday to Thursday.

Apply Here



4-Internal Audit 

MiGen Tra-Egypt is one of the leading pharmaceutical and bio-pharmaceutical companies in Egypt, Africa, and the Middle East striving to provide innovative yet affordable treatments. Making a difference and supporting our community is our main priority aligned with our mission, so we are looking for hardworking, creative, and data-driven calibers with strong communication and leadership skills allowing them to integrate well and work with diverse teams in an effective and resourceful way.

Responsibilities                     

1 . Prepare and conduct cGMP internal audit activities

2. Ensure adherence to all relevant rules and regulations

3. Evaluate effectiveness of assigned CAPAs of conducted audits.

4. Audit third parties and sub-contractors for GMP Compliance.

5. Issue new relevant SOPs and revise the approved SOP according to revision plan.

Execute quality risk management projects

Qualifications

· Previous working experience in Quality assurance for 3 - 5 years

· Audit certification is preferred.

· Bachelor degree in pharmaceutical science/ Science

· Ability to work effectively with diverse populations.

· Knowledge of auditing concepts and principles.

· Ability to persuade and influence others.

· High attention to detail and excellent analytical skills

10th of Ramadan, Sharkia, Egypt

Notes:

- Please make sure to mention your full address in the CV.

Apply Here 


تعليقات