Systems Reliability Specialist
4 weeks ago
Responsibilities
- Lead, develop/scope and execute an investigation. Strategize in collaboration with Manufacturing, Quality Operations, and SMEs - (MTech, ETS trades, QC, QOVS, QOSA, etc.), as required.
- Perform Root Cause Analysis by conducting Shop Floor Walkthrough (GEMBA), select appropriate analytical tools to collect and analyze data to determine true root cause. Leverage analytical engineering approach, the CMMS (SAP-PM), other historical or process data, as required.
- Work with Reliability professional to utilize appropriate Reliability Centered Maintenance (RCM) tools (Root Cause Analysis, Reliability modeling, FMEA's, Failure reporting, Statistical Process control monitoring, etc.), to investigate & implement appropriate Preventative actions for deviations.
- Prepare timely manufacturing/maintenance investigations (MIs) to support other functional areas as requested. And ensure reports are technically sound, clear, concise, and comprehensive.
- Work with appropriate Engineering team to identify and develop process improvements to remediate risks, within specific platform or across the site.
- In collaboration with Reliability and other APU stakeholders, evaluate appropriate CAPAs scope & action, to ensure true root cause is addressed.
- Represent SP Toronto in applicable audits (TSSA & HSE). Manage all actions required to maintain compliance to all regulatory requirements, for systems active & in service.
- Evaluate Engineering/Vendor Turnover packages for system/equipment service life support and engage appropriately to sign-off as approver or re-submit to stakeholders for correction/completion.
- Prepare for Regulatory inspections by drafting investigation briefing packages / hot topics as applicable.
- Present and defend investigations and provide support to appropriate ETS department during Regulatory inspections and other audits.
- Participate in special project improvements for ETS systems to meet GMP requirements and address inspection observations.
- Participate in cross functional Engineering Technical Services team and/or deviation review board (DRB) meetings to support timely closures of Maintenance/Manufacturing Investigations and review of CAPAs for planning and execution.
- Support updating/implementing of GMP documents or actions arising from CAPAs.
- Works within the policies, procedures and regulations as required by the Company and under the Occupational Health and Safety Act.
- Collaborate with Quality Operations (QO), Manufacturing and Subject Matter Experts (SME) to ensure deviation investigations are closed according to targeted timelines.
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