Site Name: Canada - Ontario - Mississauga
Posted Date: May 23 2020
** Only candidates currently living in Canada, with the legal right to work here, will be considered **
Facilitate and complete the L 1 audit program for all engineering
Participate in other audits as part of the 'Mission control team' as requested for L2-L3-L4 audits and act as the engineering point of contact for coordination of answer to L2 findings.
Archive the engineering related audit report and update the tracker accordingly.
Ensure that Engineering is compliant with latest applicable EHS, Quality or Engineering alerts by taking part of the assessment, definition of action plans and answer coordination when applicable.
Ensure that site keeps up to date and compliant on all (GES) Global Engineering Standards by facilitating the completion and making sure the gaps are properly identified and tracked.
Act as the expert on compliance level and provide oversight and guidance in site wide processes like Contractor Management, Legionella Management, Zero Access, etc.
Track engineering SOP & MF lifecycle. Support author to make sure all documents are current and reviewed on time to avoid compliance issues.
Participate in the Plant Recovery Report process and Root Cause Analysis as requested.
Facilitate the process of raising, tracking and managing different kind of notifications (Y3-Q4-Z1etc.) and of collecting data for reports (EVR-FVR) for all Engineering departments to make sure that actions are completed in a timely manner to avoid compliance issues.
Collect data and generates meaningful metrics to asses performance.
Lead a weekly meeting to review the KPls with all Engineering Managers, define Compliance Top 3 problems and initiate problem solving.
Collect monthly data, update the Above Site Compliance tracker and send it for approval by Engineering Lead.
Provide support to other Engineering teams as required.
University Bachelor’s Degree (Engineering, Sciences, Architectural)
In depth knowledge related to complex facility/building systems
5+ years’ experience in pharmaceutical manufacturing and packaging
Detailed knowledge of current GMP, EHS, and pharmaceutical industry practices.
Excellent technical communication skills.
Excellent computer skills
Experience with Root Cause Analysis
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