Why Patients Need YouWhether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, Importante empresa is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative Importante empresa team, youll help bring medicines to the world even faster by imagining what's possible and taking action.What You Will AchieveWorking with Pfizer's dynamic Importante empresa team, you will play a critical part in managing the maintenance and reliability Importante empresa activities involving the redesign, maintenance, and repair of utilities systems, buildings, and production/non:production equipment.As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in managing difficult issues and establishing consensus between teams.It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.How You Will Achieve ItContribute to completion of projects, manage own time to meet agreed targets, develop plans for short:term work activities on own projects.Provide Importante empresa support to develop scope of work, project execution plans, and associated Importante empresa studies for equipment and component installation, modification etc.Provide necessary operational support as needed.Review preventive and corrective work order activities, and provide equipment maintenance history review.Manage technical writing and document review.Ensure calibration compliance with (Current) Good Manufacturing Practices (part of GxP) contemporary technologies and best aseptic practices.Participate in equipment/system:based Root Cause Failure Analysis (RCFA) investigations andupdate equipment reliability plans.Partner with Production and Quality Team Leads on troubleshooting and scheduling.Promote safety within the workplace by following site safety procedures and perform proactive safety assessments, foster a safe work culture.Actively participate in site and corporate initiatives such as Communities of Practice, Limited Duration Teams.Facilitate and participate in the investigation teams created to determine root cause of exemption reports, QARs and laboratory investigation reports. Serve as a liaison between quality, Operations and regulatory/Compliance to facilitate timely closure of investigations.**Qualifications**:Must:HaveDiploma/ BTech:Electrical Importante empresa10+ years of experience / 6+ years of experienceExperience with Root Cause Failure Analysis, Equipment Criticality Ranking, PM/PdM optimization, and/or Failure Modes and Effects AnalysisUnderstanding and experience with process automation systemsStrong knowledge and understanding of Current Good Manufacturing Practices part of GxPExcellent oral and written communication skillsWorking knowledge of MS ExcelDemonstrated ability to provide technical solutions for complex problems through equipment and process understandingWorking knowledge of Food and Drug Administration Regulations, and Good Manufacturing PracticesProactive, has experience with high performance teams, strong interpersonal and project management skillsStrong written and verbal communication skillsMicrosoft Applications skillsShall be responsible for Installation, Operation and Maintenance of 33 KV line, 11 KV Line, LT Switch gears, HT Breaker, Transformer, Diesel Generators, Cooling towers and LightingTechnical Skills:Should have Knowledge on Operation and Maintenance Operation and Maintenance of 33 KV line, 11 KV Line, LT Switch gears, HT Breaker, Transformer, Diesel Generators and Cooling towersKnowledge of computation, calculation and verification of power distribution and consumption patternsKnowledge of electrical drawings and specifications of el
