Get ready! WuXi Biologics’ Summer Internship Program launches June 2, 2025. This is your chance to gain hands-on experience, learn from industry leaders, and make a real impact in the world of biologics. Whether you're in the lab, on the floor, or in the office—your journey starts here.
At WuXi Biologics, we’re shaping the future. As a global leader in biologics development and manufacturing, we support 600+ customers—including all top 20 biopharma companies.
Our 12,000+ team members drive innovation through our PROUD culture: Passion, Reward, Opportunity, Unity, and Determination. Join us and be part of something bigger.
Innovate. Grow. Make a difference. Your future starts now.
Purpose
To ensure operation of WuXi Biologics to meet regulatory and compliance requirement, strengthen QA management in document control
Job Responsibility
Responsible for the GMP document management and control;
Responsible for the production, review, release and recovery of GMP documents and blank record forms, and supervise the implementation of quality document management process in all departments.
Responsible for document electronic system maintenance and management, launch of new electronic system, etc.;
Responsible for maintenance and training of related documents process in MC system;
Responsible for the distributing, recycling, scanning and archiving of BPR and analysis records etc.;
Responsible for the archiving, loaning management and destruction of the executed records;
Responsible for the management, Labelling and putting on shelves of archive document;
Responsible for scanning archived ,Records and keeping electronic records;
Responsible for the preparation and provision of customer requirement documents;
Assist to find and provide document and records during audit
Responsible for training coordination of QA department;
Other work assigned by superior leader
Qualifications
Good Communication, teamwork and organization skills. Proficient in computer software.
Bachelor of Science or higher degree in Chemistry, Microbiology, Biochemistry or equivalent field.
The job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability
Seniority level
Internship
Employment type
Internship
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing
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