Enhance operational efficiency as a Manufacturing Compliance Specialist at Novocol Pharmaceutical in Cambridge, Canada. This full-time role focuses on investigations, corrective actions, and collaboration with cross-functional teams.

In this pivotal position, you will conduct investigations into deviations, ensuring timely identification of root causes and effective corrective actions. Your role will involve collaborating with Subject Matter Experts to facilitate problem-solving and drive investigations to completion. With your expertise in quality assurance and compliance, you will also write and review investigation reports, manage corrective action projects, and contribute to key performance indicators.

Key Responsibilities:
• Conduct investigations for deviation compliance




• Initiate timely corrective and preventative actions
• Write and review thorough investigation reports
• Facilitate cross-functional team collaboration
• Project manage corrective actions and follow-ups

Requirements:
• University degree in a related science
• Minimum 3 years in pharmaceutical QA/QC
• Proficiency in root cause analysis tools
• Robust technical writing and communication skills
• Knowledge of GMP regulations

Drive compliance and operational excellence through investigation and action management at Novocol Pharmaceutical in Cambridge.
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