Mechanic II/III, Maintenance - Day Shift (SA-mRNA) - Full-time

The Opportunity

Reporting to the Maintenance Manager, you will be responsible for the maintenance of aseptic and non-aseptic process equipment (GMP & non-GMP).

You will engage in supporting manufacturing and the execution of maintenance tasks, with minimal supervision.

• Level will be determined based on years of experience

You will report to the Team Lead, Maintenance

The Role

• 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.

• Maintain and perform corrective, preventative maintenance on aseptic and non-aseptic manufacturing equipment for in GMP & non-GMP systems.

• Maintain and provide recommendations for spare parts and PM procedures for equipment.

• Support other departments/areas to troubleshoot, test, repair, and optimize, equipment.

• Participate in the continuous improvement efforts within the site Maintenance Program (including reliability).

• Respond to alarms for assigned equipment/areas.

• Execute maintenance work for various customers with minimal interruptions.

• Work with contract service providers and support contractors executing maintenance activities.

• Support startup, commissioning and turnover of new systems in assigned area.

• Use tools and software (CMMS, PAS, Pi, PLCs, ETOPS, SAP) required to resolve equipment and process issues within all technical competencies.

• Assist other technicians and associates.

Your skills and experienceEducation

• High school diploma or Equivalent required.

• Minimum of 1 year relevant industry experience OR an Associate’s degree in relevant technical discipline with 2+ years of experience or equivalent.

Experience

• Strong desire for 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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Our Benefits

CSL Seqirus employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL Seqirus offers resources and benefits, from health care to financial protection, so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. Whether you are considering starting a family, need help paying for emergency back up care or summer camp, looking for mental health resources, planning for your financial future, or supporting your favorite charity with a matching contribution, CSL Seqirus has many benefits to help achieve your goals.

Please take the time to review our to see what’s available to you as a CSL Seqirus employee.

About CSL Seqirus CSL Seqirus is part of CSL Limited (ASX: CSL). As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. Learn more about CSL .We want CSL Seqirus to reflect the world around us

As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about at CSL Seqirus.

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