Drive innovation as a Quality Events Specialist at BIOVECTRA, now part of Agilent. This role focuses on investigations, compliance, and continuous improvement in the biotech field.

At BIOVECTRA, you will coordinate quality events and lead investigations for manufacturing deviations and process issues. Collaborating with cross-functional teams including Manufacturing, Quality, and Engineering, you will identify root causes and develop corrective actions (CAPAs) that ensure compliance with Health Canada, FDA, and EMA standards. Your expertise will contribute to enhancing patient care through better therapeutics.

Key Responsibilities:
• Lead investigations using structured tools like RCA and 5-Why
• Assess impact of deviations and contamination events




• Develop and document effective CAPAs over time
• Analyze trends for continuous process improvements
• Support audits and cleanroom compliance investigations

Requirements:
• Bachelor’s degree in Science, Engineering, or Biotechnology
• GMP manufacturing or quality experience in biologics
• Knowledge of RCA tools and investigation methodologies
• Ability to manage multiple priorities under pressure
• Proficiency with MS Office and QMS systems preferred

Utilize your expertise in quality events to advance robust processes at BIOVECTRA.
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📌 Quality Events Specialist at BIOVECTRA (Nova Scotia)
🏢 Agilent
📍 Nova Scotia