Posted in Other 30+ days ago.
Come join a company that tackles fascinating problems and find solutions to complex challenges. With deep expertise in influenza science, our team works on cutting-edge research, pioneering technologies to optimise the manufacturing process and improve the effectiveness of influenza vaccines. We operate as one integrated global organisation, drawing together expert staff from different countries to collaborate. Together, we are working on the front line to protect communities from seasonal influenza and global pandemic threats. When you join Seqirus, you join a team dedicated to making a difference in people's lives. It's a feeling of possibility, creativity, and purpose that inspires us every day.
Reporting to the Maintenance Manager, incumbent will be responsible for the maintenance of aseptic and non-aseptic process equipment (GMP & non-GMP).
Incumbent will engage in supporting manufacturing and the execution of maintenance tasks, with minimal supervision.
Shift - Days
Hours- 6AM-6PM
Follows the 2,2,3 schedule - off every other weekend
Level will be determined based on years of experience
Works closely with Quality, Engineering and Operations groups to ensure strict compliance with GMP guidelines at all times, specifically to ensure that the equipment is maintained in GMP compliance.
Maintains and performs corrective, preventative maintenance on aseptic and non-aseptic manufacturing equipment for in GMP & non-GMP systems.
Maintains and provides recommendations for spare parts and PM procedures for equipment.
Supports other departments/areas to troubleshoot, test, repair, and optimize, equipment.
Participates in the continuous improvement efforts within the site Maintenance Program (including reliability).
Responsible to respond to alarms for assigned equipment/areas.
Executes maintenance work for various customers with minimal interruptions.
Works with contract service providers and support contractors executing maintenance activities.
Provides support for start-up, commissioning and turnover of new systems in assigned area.
Uses tools and software (CMMS, PAS, Pi, PLCs, ETOPS, SAP) required to resolve equipment and process issues within all technical competencies.
Assists other technicians and associates.
High school diploma or Equivalent required.
Minimum of 3 years' relevant industry experience or an associate's degree in relevant technical discipline with 2+ years of experience OR equivalent.
Strong desire experience with trouble-shooting pharmaceutical manufacturing process problems (e.g., centrifuges, pressure test failures, electrical, autoclaves, utilities, clean steam, filling/packaging)
Experience and knowledge of maintenance principles within a cGMP Biotechnology / Pharmaceutical manufacturing environment.
Knowledge of DCS, PLC, and/or Building Automation Systems (BAS) control systems.
Proven knowledge of a Computerized Maintenance Management System (CMMS).
Ability to problem solve and troubleshoot systems in an industrial environment required
Ability to plan and organize tasks.
Interpersonal effectiveness and communication skills (written and oral) are required in order to interface across management levels and departments.
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