Sterile Area Specialist

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 life-saving 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

Job Summary:

Execute all preparation processes and supervise operators in all manufacturing steps of Parenteral Sterile Department.

Duties will include but not limited to:

1. Receive weekly production plan and follow up the execution steps.
2. Follow up product preparation, filtration, filling and capping processes and related processes according to Production Batch Record and SOPs.
3. Issue and update SOP's and batch record.
4. Follow up execution for sterile area controls according to SOPs.
5. Communicate with other related departments (QA, Validation Engineering, QC, R&D, Warehouse, etc.).
6. Record all relevant data related to SOP, Batch Records and logbooks.
7. Perform any additional tasks as requested.

The right applicant should have:

1. BSc. in pharmaceutical science or Science (chemistry section).
2. 0-3 years of relevant experience in Production Planning or Production.
3. Trainings:

• Good Manufacturing Practice
• ISO Standards 9001
• Advance knowledge Hygiene, cross contamination, cleaning process & operation controls.

Good Luck to All!