|Exova, Inc. operates over 35 facilities throughout Canada, USA and Mexico, with its head office located in Mississauga, Ontario. Four of the divisions (Materials Testing, Health Science, Environmental, Engineering & Technology) offer services in the Americas.
At Exova, Inc. our mission is to provide world-class companies with testing services that make a positive contribution to the success of their business. Committed to earning sustainable profits that attract shareholders interest and maintaining our status as a good corporate citizen, we continue to engage, develop, and retain competent people by harnessing their enthusiasm and inspiring them to excel.
Reporting to the Quality Assurance Officer, you will be responsible for assisting the QA department in internal auditing, protocol writing, KPI trending, third party audit hosting, and laboratory investigations. Applicant must be able to effectively multitask and work independently in a fast-paced, highly regulated environment.
Author method validation and instrument qualification protocols
Perform internal audits and track CAPAs to completion
Investigate deviations, perform root cause analysis, and develop CAPAs
Create quality system trend reports for management
Perform statistical analysis of data, including generation of control charts
Host client audits and assists with regulatory inspections, including responding to audit observations
Write, review, and revise SOP's
Bachelor Degree or higher in the sciences
Five years experience as a quality professional in the pharmaceutical or medical device industry
Excellent English grammar, technical writing, and proof-reading skills required
Proficient in word processing, spreadsheet management, and data entry
Internal auditing experience required, ASQ Certified Quality Auditor or ISO Lead
Experience with Master Control QMS software a plus
Positive and energized individual who is detail oriented
State or Province