Full-time
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Quality Investigations Lead – GMP & Compliance
Posted by Agilent Technologies • June 05, 2026
Description
A leading biotechnology firm in Canada is seeking a qualified professional to lead investigations and ensure compliance with industry standards. The ideal candidate will hold a Bachelor's degree in a relevant field and have GMP manufacturing experience, preferably in biologics. Responsibilities include analyzing trends for process improvement, documenting CAPAs, and participating in audits to maintain high-quality standards. This is a full-time position offering competitive pay and benefits in a rewarding environment.
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