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Department: Quality AssuranceEmployment Type: Full TimeLocation: SudairDescriptionContribute to the daily administration and coordination of training functions and events.Organize training programs and activities. Hold presentations and education resources on learning material.Coordinated orientation sessions for new employees. Review of Non-GMP Policy, Protocols, Reports, etc.Coordinate training as per the annual training calendar. To maintain all records related to training.To coordinate the training session as per the training plan in coordination with trainers.To follow up on the individual training files of employees. Oversee employee attendance and performance in training.To coordinate the training of the Qualified Saudi Program (QSP).Follow up the Responsible Sourcing activities. Provide administrative support to the departments.Develop training materials, manuals, and regulations. Maintain updated curriculum database and records.Conduct and organize workshops and orientation programs for new recruits. Run and communicate reports on events and training programs.Maintain and manage events and schedules calendar of the training department.Oversees and/or participates in the coordination, and completion of special projects and/or events. Assisting with special projects, such as process improvements.Delegating tasks and ensuring that they are completed in accordance with existing policies and procedures.Oversight of training files and all related training activities (e.g. Signing of training plans, employees certificates, etc.)All QMS Activities, like SOPs, CAPA, Oversight, Deviations, and other QA activities.Responsible for all DTC activities in coordination with the QA department.Skills, Knowledge And ExpertiseBatchelor's Degree in Pharmacy, Chemistry, Biotechnology, Biochemistry or any other related field. 3 years or more in Pharmaceutical/ Biotechnology Manufacturing Organization with EU-GMP environment.