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 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.
Evonik Vancouver QC Specialist in Burnaby employer: Evonik Canada Inc.
Evonik Canada Inc. is an exceptional employer that fosters a collaborative and innovative work culture in Burnaby, BC. With a strong emphasis on employee growth and development, we offer comprehensive training programs and opportunities for advancement within a dynamic and regulated environment. Join us to be part of a team that values accuracy, efficiency, and the importance of effective documentation management.
