Quality Manager • Mid-Level

Who you are

You have a strong background in quality management systems, particularly in the context of QC-related CMC/GMP activities. Your experience includes supporting the design and implementation of quality frameworks that ensure compliance with global regulations. You are detail-oriented and understand the importance of maintaining high standards in laboratory operations. You thrive in cross-functional environments and are passionate about fostering a culture of quality within an organization. You possess excellent communication skills, allowing you to work effectively with scientists, engineers, and business professionals. You are proactive in identifying areas for improvement and have the courage to innovate and implement changes that enhance quality processes.

What you'll do

In this role, you will support the ongoing management and continuous improvement of the Quality Management System (QMS) at AbCellera. You will be responsible for ensuring that the QC laboratory electronic systems are compliant and fit-for-purpose, enabling efficient laboratory operations. You will work closely with various teams to monitor and improve quality system processes, ensuring they align with regulatory expectations. Your contributions will play a vital role in the successful implementation of quality initiatives that impact the development of antibody-based medicines. You will have the autonomy to innovate and build scalable quality capabilities that leave a lasting impact on the organization and the industry.

What we offer

At AbCellera, you will have the opportunity to work on meaningful projects that contribute to the development of breakthrough medicines. We foster a collaborative environment where you can stretch your skills and explore new ideas. You will be part of a team that values scientific rigor and independent thinking, empowering you to make a significant impact in the field of biotechnology.