Design, develop, and implement sterile processing systems for pharmaceutical products.
Collaborate with cross-functional teams to ensure compliance with regulatory requirements and industry standards.
Conduct risk assessments and implement controls to prevent contamination or defects in the manufacturing process.
Develop and maintain documentation for sterile processes, including protocols, procedures, and reports.
Job Requirements :
8-20 years of experience in process engineering or a related field within the pharmaceutical industry.
Strong understanding of API (Active Pharmaceutical Ingredient) production processes and regulations.
Experience with project engineering, execution, control, monitoring & improvement initiatives.
Job Classification
Industry: InternetFunctional Area / Department: Research & DevelopmentRole Category: Research & Development - OtherRole: Research & Development - OtherEmployement Type: Full time