Maintenance Engineer

15 ore fa

Pisa, Tuscany, Italia Takeda Pharmaceutical Co. Tempo pieno

Job Description Previa verifica dei requisiti professionali, costituisce titolo preferenziale l’appartenenza alle Categorie Protette ai sensi dell’art 1 L. 68/99 e/o alle categorie di lavoratori che risultino percettori di interventi a sostegno del reddito e/o risultino disoccupati a seguito di procedure di licenziamento collettivo

OBJECTIVES/PURPOSE

  • Provides maintenance engineering support for pharmaceutical production equipment, with a specific process and technical focus on sterile filling lines, isolator technology, vial washers , depyrogenation tunnels, stopper processors, autoclaves.
  • Acts as a technical interface between Maintenance and Process Engineering, combining equipment reliability and maintenance expertise with a solid understanding of aseptic filling processes and contamination-control requirements.
  • Supports troubleshooting on corrective and preventive maintenance activities, in accordance with EHS and GMP rules, for GmP/non-GmP equipment /systems at the Pisa site, in support of production and filling plans.
  • Provides support on spare-parts management, maintenance documentation, maintenance contract review, SOP review within the assigned area of expertise.

ACCOUNTABILITIES

  • Supports the Maintenance Department in ensuring safe, compliant and reliable performance of assigned pharmaceutical equipment, with particular attention to sterile filling and isolator systems and ancillary systems.
  • Works closely with Process Engineering to investigate production problems, recurring alarms, stoppages, process deviations and performance losses involving sterile filling equipment.
  • Supports troubleshooting, RCA, technical investigations, CAPA and continuous improvement in accordance with EHS, cGMP, Quality and Data Integrity requirements.
  • Complies with EHS requirements and supports their implementation during maintenance activities.Supports the team in promoting the culture of operational safety and procedures development.
  • Works with RCM tools, dashboards and data analytics to increase OEE of filling line.
  • Supports spare-parts management for assigned equipment, including criticality assessment, identification of technical requirements, notification of system or inventory gaps and proposal of improvements.
  • Develops and maintains strong technical knowledge of the assigned equipment and process, including operating principles, critical parameters, equipment documentation, interfaces and failure modes.
  • Coordinate and technically supervises suppliers and contractors for maintenance, specialist support, service visits and improvement activities, ensuring compliance with EHS and site requirements.

CORE ELEMENTS RELATED TO THIS ROLE

  • Maintenance role with a differentiated process-engineering orientation and specialist focus on sterile filling technology, while keeping an olistic perspective on site activities.
  • Acts as a technical interface between Maintenance and Process Engineering for isolators, aseptic filling equipment, vial washers and depyrogenation tunnels.
  • Field-oriented contributor able to connect process behaviour, machine functionality, maintenance history and compliance requirements.
  • Contributes to site capability building through technical support, knowledge sharing, documentation, structured troubleshooting and dissemination of lessons learned.

DIMENSIONS AND ASPECTS

  • Technical/Functional (Line) Expertise
  • Applies engineering knowledge to maintenance and process-related issues on sterile pharmaceutical equipment.
  • Supports equipment reliability, maintenance strategy, technical documentation, validated-state maintenance and compliance with cGMP, EHS and Data Integrity requirements.
  • Leadership
  • Promotes technical excellence, safe behaviours and structured problem solving
  • Collaborates with cross-functional teams for problem solving and technical implementation / assessment
  • Decision-making and Autonomy
  • Performs assigned activities autonomously within approved procedures, defined priorities and the boundaries of the role.
  • Evaluates technical evidence, proposes actions and escalates significant risks and decisions to the Maintenance Lead and relevant Process Engineering or Quality stakeholders.
  • Interaction
  • Maintains regular interaction with Maintenance, Process Engineering, Production, Quality, Automation, Reliability, EHS, Validation and external suppliers.
  • Innovation
  • Uses equipment data, failure history and process observations to identify recurring issues and propose sustainable improvements.
  • Complexity
  • Operates in a regulated sterile-manufacturing environment where equipment reliability, aseptic-process performance, validated state, safety and production continuity are closely interconnected.