Job Description & How to Apply Below
Step into the role of SAS Stability Coordinator at Septodont in Cambridge, Canada. Oversee and manage stability studies, ensuring quality control in pharmaceutical products.
This position reports to the Stability and Analytical Services Manager and focuses on the comprehensive management of stability programs and data analysis. You will prepare technical documents, manage schedules, and troubleshoot stability chambers while engaging in proactive monitoring of samples. With at least 2 years in the pharmaceutical sector, you will contribute to regulatory compliance by maintaining rigorous quality standards.
Key Responsibilities:
• Manage and execute stability studies and risk assessments
• Document protocols and specifications in Electronic Management Systems
• Request, log, and verify stability samples accurately
• Communicate with vendors for equipment support and repairs
• Assist in preparing materials for regulatory assessments
Requirements:
• Degree in Chemistry or equivalent scientific discipline
• At least 2 years of experience in stability management
• Proven competence in LIMS and Microsoft Office Suite
• Detail-oriented with excellent organizational skills
• Effective communicator both verbally and in writing
Your expertise in stability testing and data management will support Septodont's mission to enhance public health through quality products.
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