Job Description Your missions Support end-to-end manufacturing processes for biologics production (drug substance) Monitor and optimize process performance to ensure efficiency, quality, and compliance Troubleshoot process deviations and implement corrective and preventive actions (CAPA) Collaborate with cross-functional teams including Production, Quality, Validation, and Engineering Contribute to process validation activities and continuous improvement initiatives Ensure adherence to GMP, safety, and regulatory requirements Support documentation including SOPs, batch records, and technical reports
Your profile Bachelor's degree in Chemical Engineering, Biotechnology, Bioprocess Engineering, or related field 2–5+ years of experience in biopharmaceutical or biologics manufacturing Strong understanding of GMP and regulatory standards Experience in drug substance processes such as fermentation, purification, or filtration Familiarity with process validation and troubleshooting in a ma...