Take your career to recent heights as a QC Specialist with Evonik in Vancouver. Shape high-quality drug development initiatives by enhancing operational capabilities and supporting project management. Bringing 5 to 8 years of industry experience, you will be pivotal in optimizing QC processes and ensuring compliance with GxP standards.

Your responsibilities will include managing schedules, conducting reviews, and ensuring the proper handling of materials and samples across various projects. Key Responsibilities:
Prepare QC master schedules in line with business plans
Ensure timely testing of stability samples
Conduct peer reviews of raw and stability materials
Collaborate with external labs for testing requirements
Support various QC team projects and initiatives Requirements:
Degree in Chemistry, Biochemistry, or related field
5 to 8 years in the biopharmaceutical sector
Familiarity with program management tools
Solid writing and communication skills
Detail-oriented approach to data management Enhance your QC expertise and contribute to creative drug solutions at Evonik in Vancouver.

📌 Evonik Vancouver Qc Specialist Burnaby
🏢 Evonik Canada
📍 Burnaby