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 robust analytical abilities Leverage your QC expertise at Evonik and shape the future of biopharmaceutical manufacturing in Burnaby.

📌 Evonik Qc Specialist Opportunity, Burnaby
🏢 Evonik group
📍 Burnaby