Maintenance Mechanic I/II/III (Process)

You are responsible for the maintenance of aseptic and non-aseptic process equipment (GMP & non-GMP) in the Bulk and Fill Finish, Inspection, labeling, and packaging areas.

You will engage in supporting manufacturing and the execution of maintenance tasks. You will report to the Team Lead, Maintenance.

Location: Onsite in Holly Springs, NC

• Work 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, assess and troubleshoot equipment and systems.

• Execute maintenance work for various customers with minimal interruptions.

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

• Provides support for start-up, 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.

• High school diploma or equivalent required

• Minimum of 1 year relevant industry experience, OR an Associate's degree in a relevant technical discipline, with 2+ years of experience OR equivalent

Experience

• Strong desire and/or experience with trouble-shooting pharmaceutical manufacturing process problems (e.g., centrifuges, pressure test failures, electrical, autoclaves, utilities, clean steam, filling/packaging, pneumatic systems, vision systems)

• Experience with maintenance principles within a cGMP Biotechnology / Pharmaceutical manufacturing environment.

• Knowledge of DCS, PLC, and/or Building Automation Systems (BAS) control systems.

• Knowledge of a Computerized Maintenance Management System (CMMS).

Benefits

Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. Learn more about some of the benefits you can participate in when you join Seqirus.

Our Benefits

Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. Learn more about some of the benefits you can participate in when you join Seqirus.

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

As a global organisation with employees in 35+ countries, CSL embraces diversity, equity and inclusion. Learn more about Diversity, Equity & Inclusion at Seqirus.