Maintenance Engineer I - Maintenance IT - System Admin
Goa, India, 403722
Who we are
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
Teva’s Equal Employment Opportunity Commitment