Join Evonik as a QC Specialist in Burnaby, BC, and play a crucial role in enhancing quality control processes while ensuring operational excellence. This position supports multiple projects within a agile CDMO environment.
As a full time team member, your role will involve collaboration with various stakeholders to prioritize QC efforts. With a focus on strategic planning and operational efficiency, you'll prepare testing schedules and manage quality documentation, ensuring compliance with regulatory standards.
Key Responsibilities:
• Manage QC activities and optimize scheduling
• Provide operational insights for client projects
• Draft specifications and sampling plans accurately
• Supervise stability studies and track sample testing
• Coordinate with project teams on reference standards
Requirements:
• BSc or MSc in Chemistry or related fields
• 5 to 8 years’ experience in biopharmaceuticals
• Background in Quality Control is advantageous
• Skilled in project/resource management techniques
• Detail-oriented with robust analytical abilities
Leverage your QC expertise at Evonik and shape the future of biopharmaceutical manufacturing in Burnaby.
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