Take your career to new 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 plansEnsure timely testing of stability samplesConduct peer reviews of raw and stability materialsCollaborate with external labs for testing requirementsSupport various QC team projects and initiativesRequirements:Degree in Chemistry, Biochemistry, or related field5 to 8 years in the biopharmaceutical sectorFamiliarity with program management toolsStrong writing and communication skillsDetail-oriented approach to data managementEnhance your QC expertise and contribute to cutting-edge drug solutions at Evonik in Vancouver.