לוח אפשרויות קריירה - הדרך החכמה להייטק

How you’ll spend your day
•    Carry out Preventive maintenance of all computer system of ICS (PLC, HMI, IPC, and SCADA).•    Troubleshooting and diagnosing hardware and software problems, including Server, desktop, laptop, LAN and Instrument/Equipment System.•    Install and configure Standalone instrument/Equipment/ Output devices at the premises.•    Managing and coordinating with vendor to resolve the issue of QC, QA laboratories instrument software.•    Ensure electronic records and electronic signatory system data is maintained and routinely backed up.•    Carry out FAT / SAT/ computer system validation for new system and other installation/Qualification supports in old systems as applicable.  •    User Management in computer system (QC, QA firmware based instrument/equipment and Production computers).•    Preparation of Annual planner for computer system validation.•    To plan and regulate the work of technical force during the shift for smooth functioning of the machines and other maintenance related activities.•    Planning and implementation of periodical servicing, annual maintenance contracts and other Engineering related works.•    Adhere Quality and safety standards, procedures, practices & ensure implementation of the same.•    To ensure Data integrity compliance with respect to laid down procedures and systems.•    Ensure the effective shift handover and takeover in order to make the effective communications within the team and CFT as well.•    Maintain the log books in good condition with required GDP requirements. •    Perfrom and Ensure On time closure of Safety and quality tasks.•    Analysis the Preventive , breakdown maintenance and implement best practices in order to improve OEE & change the approach from breakdown to PM.•    Maintain the inventory of critical spares and consumables by tracking consumption and monitoring of stocks.•    Ensure the ontime closure of the trainings.•    Monitor cGMP compliance in the impact domain and report any incident / cGMP deviation to the Shift In charge.•    Maintain online documentation and timely entries in all document in cGMP environment and their supporting documents•    Prepare and maintain engineering documents inline to cGMP and GEP & Global Engg Teva Standards •    Propose and implement new idea to enhance production, optimise the use of consumable goods and maximum utilization of resources•    Provide new ideas and simplify processes to reduce process cycle time and achieve new targets•    Always keep ready the systems, equipments, facility for the audits and production activities. •    Share and comply the safety observations.•    Ensure the ontime closure of planned maintenance, AMC‘s, BM‘s, Calibrations, Validations.•    Face the internal and external audits as applicable.  •    Implement action plans for improving on deficiencies observed through internal / external audits/inspections.•    Interact with OEMs for projects , automations, alternate vendor development , quality issues and maintenance.Your experience and qualifications
I.T.I/ Diploma/Engineering Degree
6+ years of experience