Temporary Pu Process Specialist

Sandoz

Perform initial investigation of all incidents in the area Second level trouble shooting support to the operator End to end production plan follow-up (Multiple product groups during the shift coverage) MES and SAP key user to inform on call IT support Involve OpEx projects HSE incidents reporting & action follow-up SOP review & revision•Area responsibility and daily walkthrough Operator Training Batch record review and handover to QP for release responsibility • To make the necessary coordinaton and organisation studies to ensure that production process and the relevant procedures are performed properly and on time. • To conduct works that will increase the production and improve the quality, minimize the wastage. • To document Batch records and deviations on regular basis. • To check whether the production is carried out in compliance with production protocols and processed at the time of production, at the end of the production to make final check and approve of the protocols. • To prepare the production prescriptions and revise them. • To ensure that the training program is composed and actively implemented. • To lead the production consumption material needs. • To ensure that the working area is kept clean and neat in accordance with GMP rules. • To coordinate with all directorates related to the production and help the division work efficiently.

To continually observe the behaviors of the personnel and insure compatible working within the divisions and support it. To improve the personnel management by taking the personnel policy into account. • To build the most rational and efficient relation between the labor and the machine. • To ensure that the anticipated flexible time and multiple-shift system is implemented. • To insure physical order of the production areas and preserve it. To appropriately assign and manage the employees reporting to himself/herself in order to make the most effective use of the working time. • To motivate his/her team positively. • To prepare and achieve Annual Performance Targets • To ensure continuous GMP and technical of his/her personnel in line with GMP rules and according to the approved training program. • To ensure the initial and periodical training of production personnel and contribute to training programs. • To ensure performance criteria deployed by top management are achieved. • To support his personnel in the preparation of annal performance goals and the realization of them. To follow that GMP requirements defined by MOH, Novartis / Sandoz Quality Manual are completely and effectively implemented. To follow Novartis  Information Security  policy & rules. To comply with Novartis Privacy declaration & procedures. Responsible for all aspects of health, safety, quality, and environment at the responsible area. Ensure implementation of needs regarding local legislation, Novartis HSE policy, GuideLines / Procedures and Business Continuity Guides in responsible operations. Conduct the duties given in scope of Novartis Emergency Response Procedures. Implementation of Emergency preparedness requirements according to global and local requirements at the responsible area. Ensure all assignment and schedules prepared considering employees health and safety, To know workplace risks in their area of responsibility and execute instruction and procedures determined according to risk assessments. Ensure implementation of all precautions to reduce the risks. Ensure proper workplace safety training are given to the employees. To offer proper precautions to reduce the risks. Ensure the proper Personal Protection Equipment (PPE) is given to all employee and in use. To inspect and follow up associates (including contractors) to ensure compliance with HSE & Quality rules, and give them notifications on the spot, and/or verbal or written warning if necessary.

Minimum requirements:Bachelor Degree English - Advanced 0-5 years relevant experience.