工作地点:中国上海外高桥保税区 To apply, please submit your CV and research summary to yan_lin@wuxiapptec.com Key accountabilities: 1. Able to applies expertise to cell line development projects to produce stable cell lines suitable for clients’ human clinical trials with experience of transfection, selection and amplification protocols 2. Design experimental plans, lead cell line development execution. Critically analyze cell culture data, interpret and integrate experiment results. 3. Responsibilities include regular communications with external clients to update project status, writing interim and final technical reports. Maintain records sufficient to support regulatory filings 4. Investigate, create and develop new methods and technologies for advancements in the area of cell line development 5. Contributor in a formulation team and then lead the team in Shanghai, China to support formulation development, stressed studies, container closure system selection and process development for protein drugs or other parenteral drugs. 6. Contribute to and then lead pre-formulation studies to characterize candidate molecule and elucidate degradation pathways to gain understanding of stability challenges and develop strategies for stabilization. 7. Collaborate with analytical, cell culture and purification and fill/finish teams to lead the development and transfer of biosimiliars, new formulations, container closure systems and fill-finish technology to support toxicology study, clinical development, tech transfer, and process validation for internal or external partners. 8. Collaborate with vendors, draft and then execute qualification of formulation and fill/finish instruments and equipments. 9. Plan, assign, direct and evaluate the work of technical staff when assigned to the project to meet aggressive project timelines. 10. Supervise lower level scientists and evaluate their performance. 11. Present results internally and externally at weekly and monthly meetings with customers as well as industrial and scientific conferences. REQUIREMENTS: 1. We are seeking a candidate with PhD degree and 0-2 years industry or postdoc experience. 2. Or Ph.D. degree preferably in pharmaceutical chemistry, biochemistry, biophysics, biology or engineering discipline. 3. Have background in one of the following fields: biochemical or biological engineering, cell/molecular biology, biochemistry, or microbiology. 4. Hands-on experience in mammalian cell culture or microbial fermentation using bioreactors is preferred 5. Experience with recombinant protein expression is a plus 6. Have strong expertise in process optimization, scale-up and technology transfer. 7. Experience with medium optimization, DoE studies, regulatory submission to the FDA/EMEA and personnel management is preferred. 8. Key aspects of the position include coaching, mentoring and managing junior staff members, 9. Technical oversight of study design, execution and results interpretation. 10. Ability to accomplish the described