Quality Control Associate at CCRM

Advance your career as a Quality Control Data Reviewer Associate I at CCRM in Toronto. Be part of a pioneering team in regenerative medicine and quality assurance.

As a QC Data Reviewer Associate I, your role will encompass reviewing critical QC documentation and ensuring adherence to Good Manufacturing Practices. Your responsibility includes validating data accuracy, preventing non-compliance issues, and assisting in quality investigations. By maintaining the highest quality standards, you will help propel innovative cell and gene therapies to market.

Key Responsibilities:

• Assess QC documentation for GMP compliance

• Validate all data and calculations thoroughly

• Monitor reagent expiry and equipment calibration

• Report on deficiencies and participate in corrections

• Conduct timely data reviews before due dates

Requirements:

• Bachelor's in Science with 3+ years in GMP settings

• Prior experience in quality assurance is a plus

• Strong understanding of QC processes

• Capable of independent and collaborative work

• Proficient in English with strong communication skills

Contribute to CCRM's significant advances in medical technology while ensuring product excellence in quality management.
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