Description: Our client is a leading pharmaceutical company based in Kurdistan- Iraq.
Develop various robust pharmaceutical dosage forms based on sound science and quality risk management.
Develop process that can be scalable and optimized to commercial size based on current scientific approaches and in accordance with current regulations.
Develop department procedures and implement GLP and GMO understanding including SOP.
Provide thorough product development reports and practical batch manufacturing record and technology transfer.
Projects prioritization according to the company plan
Knowledgeable of product registration requirements
Coordinate with Regulatory Affair for file submission in timely manner and be able to answer all deficiencies.
Provide regular reports on project status and effective communication to overcome and offer solution to any issues related to project progress.
Prepare project updates, presentations and reports for senior management
Review and manage technical data and documentation to ensure timely action, compliant storage and efficient retrieval
Develop and maintain suitable project schedules, budgets and risk mitigation plans with project teams and external service providers
