Cytiva Analytical Development Co-op Vancouver
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As an Analytical Development Co-op, you will engage in quality control testing of raw materials and finished products. This on-site role within the BioPharmaceutical Operations group involves utilizing techniques like HPLC and LC-MS. Your responsibilities will include maintaining accurate documentation, preparing technical reports, and supporting daily lab operations while adhering to GMP standards.
Key Responsibilities:
• Perform quality control testing on RNA Lipid Nanoparticles
• Document laboratory activities in compliance with GMP
• Assist in preparing analytical findings and reports
• Support lab operations including equipment calibration
• Manage reagent preparation and inventory
Requirements:
• Pursuing a degree in relevant scientific fields
• Experience with analytical or bioassay techniques
• Familiarity with chromatography and gel electrophoresis
• Hands-on laboratory experience required
• Strong understanding of data integrity principles
Elevate your career by contributing to significant advancements in human health at Cytiva.
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