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 dynamic CDMO setting.
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 strong analytical abilities
Leverage your QC expertise at Evonik and shape the future of biopharmaceutical manufacturing in Burnaby.