Production Pharmacist

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

About The Job

Participate in production processes in the production areas of MiGenTra Egypt, and all related tasks ensuring successful fermentation process to achieve the company's goals.

Responsibilities

1. Strongly obey all GMP rules related to the field of employment. Comply with the IMS requirements, record all processes within the good documentation practice
2. Comply with the annual objective of departments, Company's policy and the predetermined KPIs
3. Supervise the technicians during the production process.
4. Issue new SOPs and revise approved SOP according to revision plan and current needs, initiate change controls according to instructions.
5. Notify timely supervisor and QA about all incidents while participating in investigation and assessment of incidents, deviations and changes, perform root cause analysis.
6. Contribute to SMART corrective and preventive actions for audit findings, implement CAPA, additional controls, change control actions, annual report actions and management review actions according to instructions.
7. Contribute to quality risk management projects, support continuous process improvements, report and support assessing environmental hazard aspects and impacts, report and support assessing health and safety risk assessment.
8. Strongly cooperating with other departments (for instance DSP, QA, QC, R&D, engineering, warehouse) aiming at smooth and efficient production and process flow.
9. Perform any additional tasks as requested related to the field of employment.

Requirements:

Education: bachelor's degree in Pharmaceutical Science.

Experience: 0-1 years of relevant experience.

Location:
10th of Ramadan