Major responsibilities

• Full time facility management for Suzhou 12#, 8# and Shanghai Xinsi site.
• Manage the procurement process for spare parts, maintenance and modification projects related to engineering equipment and system.
• Archive for engineering documentation and drawing, such as Shop drawing, as-build drawing, GMP drawing, SOP, SMP, Record, and hand-over documentation of projects.
• Ensure archived documents comply with company quality systems and GMP requirements.
• Drive project EHS and GMP compliance.
• Participate in quality activities, such as deviation, CAPA, CC and others.
• Provide timely document retrieval, loan, and copy services for project teams, operation departments, and other functional units.
• Develop and implement annual, foundational and on-job training plans, track training execution and maintain staff training files.
• Participate in and support internal and external audits and assist in the implementation of audit corrective actions.

Education, Qualifications, Skills and Experience

• Education background: Bachelor or above.
• At least 2-3 year work experience in Bio pharmaceutics manufacture (Experience working in a foreign company is preferred.)or related industrial company.
• Have the acknowledge of facility and process equipment management.
• Have the experience of document management.
• Have the background and acknowledge of GMP system.
• English skills: Fluent oral English, listening, Reading, Writing.