Biotechnology Production Pharmacist At Minapharm Pharmaceuticals
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
Plant: MiGenTra Egypt
Department: Manufacturing - Downstream
Job Summary:
Participate in downstream production processes in the mAB production areas of MiGenTra Egypt , and all related tasks ensuring successful purification runs to achieve the company’s goals.
Duties:
1.Perform mAB downstream processes according to production plan, and fulfil all duties required to ensure production (e.g. calibration of equipment, issuing materials and tools dispensing order, follow up of the stock). 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, participate in investigation and assessment of incidents, deviations and changes, perform root cause analysis and 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.
6.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.
7.Strongly cooperate with other departments (for instance BMP, USP, QA, QC, R&D, engineering, purchasing, warehouse) aiming at smooth and efficient production and process flow.
8. Perform any additional tasks as requested related to the field of employment.
Job Requirements:
A. Experience: 0 - 2 years of Experience
B. Education: Minimum Bachelor’s degree in Biotechnology or Pharmaceutical Science.
Work under pressure.
Ability to understand and follow written instructions.
Computer literate.
Proficient in English Language.