Jobs in Edmonton, Canada

About the role

We are seeking a detail-oriented Coordinator, Compliance to support pharmaceutical manufacturing operations at our Biotechnology Business Development Centre. This role is responsible for creating and managing GMP-compliant technical documentation, ensuring regulatory adherence, and supporting batch record review, audits, and quality processes. The successful candidate will be working cross-functionally with Production, Quality, and Engineering teams and will help maintain inspection readiness and uphold data integrity in a fast-paced, regulated environment, contributing to critical drug development and manufacturing initiatives.

What you'll bring

• Bachelor’s or Master’s degree related to pharmaceutical product manufacture.
• An equivalent combination of education and experience will be considered.
• 1-3 years of experience in cGMP regulated pharmaceutical manufacturing environment.
• Ability to take direction.
• Enthusiastic and willing to learn.
• Strong oral and written communication.
• Good interpersonal skills with the ability to interact with people at all levels with sensitivity and tact
• Applications submitted without a resume AND cover letter will not be reviewed.
• Experience in pharmaceutical manufacturing is preferred.
• Strong technical writing skills, independently create SOPs, investigate and write deviations, initiate change controls is preferred.

Benefits