Specialist in Quality Systems Management

Join AbCellera as a Specialist in Quality Systems Management, focusing on QC-related activities and ensuring compliance with stringent global standards.

Your role will make a meaningful impact on data-driven laboratory operations.

This position requires you to support and enhance the Quality Management System (QMS) for QC operations within a GxP-regulated environment. By overseeing QC laboratory eSystems, you will help maintain compliance and operational excellence. Your initiative and innovative mindset will be crucial for continuous improvements within our quality framework.

Key Responsibilities:

• Continuously improve QC QMS framework and activities

• Administer QC electronic systems for effective laboratory workflows

• Identify needs for QC data architecture and system enhancements

• Support system changes and training for end-users

• Collaborate with teams to ensure eSystems' compliance

Requirements:

• 3+ years experience in a GxP quality systems role

• Bachelor’s in a relevant scientific or engineering field

• Strong background in continuous improvement methodologies

• Knowledge of drug development processes and regulations

• Experience with eSystems in GMP environments

Utilize your experience to contribute positively to AbCellera's innovative efforts.
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