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Non-Sterile Production pharmacist in IPC department which responsible to ensure all products, in process materials, production facilities and process comply with the Company’s Quality Management standards and Government’s cGMP requirements through proper monitoring procedures, effective training program and up-to-date documentations
Job Responsibility
Management of In-process control Process
IPC Documentation Management
Calibration / Qualification Plan
IPC Capex
Make annual plan for providing the department with process consumables
SMS Activities
Tablet compression sets Management
Working as Second Line for Solids and manufacturing areas and Dispensing Area
Responsible of Procurement activities through managing all OPEX & CAPEX for NS-production unit
HSE & Energy Role
Requirements
Bachelors' degree of Pharmacy
0-2 years of experience
Very Good written and spoken English
Strong communication, time management, and analytical skills
Ability to work under stress and in teams
Proactive, detail-oriented, and committed to continuous improvement
Leadership and strategic thinking capabilities
Good Manufacturing Practices (GMP) & Good Documentation Practices (GDP)