Description

Support quality assurance operations within a GMP manufacturing environment by reviewing batch records, clearing backlogs, and managing room releases.

This role is on-site.

Responsibilities

• Review executed batch records and production documents to clear existing backlogs.
• Manage day-to-day operational tasks including room release and equipment changeover reviews.
• Investigate quality events such as deviations, lab investigations, CAPAs, and change controls.
• Review technical documentation including SOPs, COAs, protocols, and reports.
• Collaborate with Manufacturing, Quality Control, and Facilities teams to resolve quality matters.

Required Skills

• 1-2 years of experience working within a GMP industry.
• Bachelor's or Master's degree in biological sciences, analytical chemistry, or chemical engineering.
• Experience reviewing SOPs and COAs.
• Strong critical thinking skills for evaluating new procedures or process improvements.
• Ability to work on-site in Toronto.

Preferred Skills

• Prior experience within the biotechnology industry.

Key Skills

Education

Bachelor's