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Evonik QC Specialist
Job Description & How to Apply Below
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
• Strong writing and communication skills
• Detail-oriented approach to data management
Enhance your QC expertise and contribute to innovative drug solutions at Evonik in Vancouver.
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