Drive quality assurance initiatives as a QA Compliance Specialist with Bora Pharmaceuticals. This full time role offers the chance to ensure GMP compliance in global pharmaceutical projects.

As a QA Compliance Specialist for an 18-month fixed-term at Bora Pharmaceuticals, you will play a key role in quality support across various departments, ensuring all regulatory requirements are met during product transfers. Utilize your knowledge of compliance frameworks to manage quality documentation and supplier assessments effectively.

Key Responsibilities:
• Provide quality support for project transfers
• Approve master data and other compliance documents
• Analyze processes to identify and mitigate risks
• Lead investigations using root cause analysis tools
• Engage in drug establishment license management

Requirements:
• Bachelor’s degree in a science-related field
• Minimum 5 years of relevant quality experience
• Strong understanding of global GMP and regulatory standards
• Proficient in Microsoft Office and data management tools
• Expertise in risk management principles

Make a difference in pharmaceutical quality assurance at Bora Pharmaceuticals.
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📌 Quality Assurance Specialist for Bora Pharmaceuticals (Ontario)
🏢 Bora Pharmaceutical Services
📍 Ontario