Global Manufacturing (US & APAC) was established to strengthen WuXi Biologics' global manufacturing network and capabilities, enhance cross-regional operational efficiency and organizational resilience, and support the long-term development of the company's CRDMO business. The organization consists of the Drug Substance Clinical Manufacturing sites in Shanghai and Suzhou, manufacturing sites in Cranbury, New Jersey and Worcester, Massachusetts, and WuXi Biologics' Singapore site. •You will be receiving technical trainings and soft skills trainings from companies’ Subject Matter Experts (SMEs). •You will have a mentor to help customize your individual development plan. The mentors are graduated from the top schools and have plenty of industrial experiences. The mentor will also follow your growth and make adjustment as needed to help your growth. •You will also have area coach to help you enhance knowledge and guide you on day-to-day job. •You will receive 6-12 months of training in China (Suzhou, Shanghai), with opportunities to work in overseas bases such as the US Cranbury site. •You may have opportunities to work in different functions to obtain in depth knowledge to develop area of expertise. •You may receive tasks to work with cross-functional team to polish soft skills (communications/transversal leadership/negotiations, etc.) •You may be directly involved in the new drug development projects from domestic and foreign customers. •You may have opportunities to understand new drug projects from multiple dimensions such as production project management, production operations, auditing, and manufacturing technical support. In addition, there is also rotation job opportunities provided to the trainees. See below examples of the areas that can be rotated in: • GMP production (Drug Substance /Cell Banking) • Project Management • Clinical Manufacturing Technical Support • Manufacturing Operation • Manufacturing Compliance Job Responsibilities (assignment vary based on your background): • Perform daily duties focused on DS manufacturing process tech transfer, scale up and cGMP manufacturing operation. • Perform cGMP cell bank manufacturing activities. • Assist to establish DS/Cell Banking manufacturing operation system including but not limited to operation documentation/training system, project production schedule and follow up. • Trained to be function lead of DS/CB projects to coordinate with clients and internal departments to facilitate the success drug substance/product/cell banking manufacturing. • Perform experiments in the lab for GMP satellite runs or assist in experimental design to support complex deviation investigation or other studies to support GMP operations. • Author cGMP documents and presentations for internal and external reporting. • Draw process flow diagram and assisted in map out the process flow for different business processed to identify improvement opportunities. • Assist in data analysis and modeling to provide insights on manufacturing. • Assist in conducting client audit to prepare audit notes. • Assist to develop training programs for the DS/CB manufacturing team, and align with Site and Corp employee training and development policies. • Performs other duties as assigned. Who you are: • Recent undergraduate, master's, or doctoral graduates. • Majors in Biology, chemical engineering, pharmaceutical related fields • Strong critical and analytical thinking • Self-starter and be creative • Can adapt to fast speed working environment and handle pressure at work • Excellent interpersonal communication and presentation skills • Excellent written skills in English. Fluent in English as the primary language of communication. • Able to adapt to and embrace a multicultural environment. • Willing to follow arrangements to work at various sites in either China (Suzhou, Shanghai) or US. • Foreign nationals are welcome to apply