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