Maintenance Specialist
4 settimane fa
As a Maintenance Specialist at Novartis, you will be responsible for planning and coordinating maintenance and calibration activities, project execution, and continuous improvement at site level. This includes ensuring equipment operates to required HSE, Quality, Environmental, and Reliability standards.
About the Role- Develop and implement strategies for equipment maintenance and calibration.
- Lead or contribute to equipment, utility, and facility improvement projects.
- Ensure compliance with HSE, Quality, Environmental, and Reliability standards.
- Manage maintenance improvement projects and initiatives.
- Establish maintenance and calibration plans.
- Coordinate maintenance and calibration activities.
- Plan resources for maintenance and calibration.
- Allocate work for maintenance and calibration to technicians.
- Maintain Master Instrument Inventory (MII) and Master Equipment Inventory (MEI).
- Enter work orders into CMMS for maintenance and calibration.
- Develop method statements for maintenance and calibration.
- Perform risk assessments for maintenance and calibration.
- Provide frontline support for technicians.
- Supervise maintenance and calibration work.
- Assess quality impact and release after maintenance.
- Assess equipment fit for purpose.
- Set up maintenance for new equipment.
- Develop, monitor, and improve KPIs for maintenance and calibration.
- Execute FMEA and define maintenance type for each asset.
- Manage technical and engineering changes.
- Investigate deviations.
- Create and maintain engineering documents.
- Plan spare parts.
- Manage stores for spare parts.
- Establish vendor contracts.
- Identify technical solutions.
- Prepare equipment specifications and system requirements.
- Prepare, review, and approve drawings and documents.
- Develop project turnover plans.
- Perform new equipment FAT/SAT/inspections.
- Perform commission activities.
- Manage project deficiencies and deviations.
- Perform provisional and final project handovers.
- Provide technical troubleshooting during PQ and validation.
- Develop periodic requalification plans.
- Execute periodic requalification plans.
- Develop and implement coding and recipes.
- Monitor automation hardware.
- Design, implement, and maintain historian configurations.
- Implement software change controls.
- Design and implement Master Batch Records (MBR) for MES.
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Division: International
Business Unit: Innovative Medicines
Location: Italy
Site: Ivrea
Company / Legal Entity: IT58 (FCRS = IT058) AAA Italy Srl.
Functional Area: Technical Operations
Job Type: Full time
Employment Type: Regular
Shift Work: No
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